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HBA_ISH_GeneList.txt
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HBA_ISH_GeneList.txt
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"TECHNICAL WHITE PAPER:
COMPLETE LIST OF GENES CHARACTERIZED BY IN SITU HYBRIDIZATION IN ADULT HUMAN BRAIN STUDIES"
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
A2M 2 alpha-2-macroglobulin extracellular matrix Alzheimer’s VEC
AANAT 15 arylalkylamine N-acetyltransferase metabolic enzyme protein evolution
AATF 26574 apoptosis antagonizing transcription factor transcription factor other neurodegenerative
ABAT 18 4-aminobutyrate aminotransferase metabolic enzyme epilepsy interneuron
ABCD1 215 "ATP-binding cassette, sub-family D (ALD), member 1" transporter other neurodegenerative
ACCN1 40 "amiloride-sensitive cation channel 1, neuronal (degenerin)" ion channel autism
ACE 1636 angiotensin I converting enzyme (peptidyl-dipeptidase A) 1 metabolic enzyme Alzheimer’s
ACHE 43 acetylcholinesterase (Yt blood group) metabolic enzyme Alzheimer’s
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
ACTB 60 "actin, beta" cytoskeletal protein mental retardation
ACTN2 88 "actinin, alpha 2" cytoskeletal protein schizophrenia
ADAM23 8745 ADAM metallopeptidase domain 23 extracellular matrix autism
ADAMTS8 11095 "ADAM metallopeptidase with thrombospondin type 1 motif, 8" extracellular matrix
ADAMTSL5 339366 ADAMTS-like 5 extracellular matrix
ADCY1 107 adenylate cyclase 1 (brain) signal transduction
ADCY2 108 adenylate cyclase 2 (brain) signal transduction
ADCYAP1 116 adenylate cyclase activating polypeptide 1 (pituitary) peptide ligand autism protein evolution
ADM 133 adrenomedullin peptide ligand interneuron or VEC
ADORA1 134 adenosine A1 receptor GPCR
ADORA2A 135 adenosine A2a receptor GPCR other neurodegenerative
ADORA3 140 adenosine A3 receptor GPCR
ADRA1A 148 "adrenergic, alpha-1A-, receptor" GPCR
ADRA1D 146 "adrenergic, alpha-1D-, receptor" GPCR
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
ADRA2A 150 "adrenergic, alpha-2A-, receptor" GPCR depression layer 6b
ADRA2B 151 "adrenergic, alpha-2B-, receptor" GPCR
ADRB2 154 "adrenergic, beta-2-, receptor, surface" GPCR obesity
ADRBK1 156 "adrenergic, beta, receptor kinase 1" kinase
ADRBK2 157 "adrenergic, beta, receptor kinase 2" kinase bipolar
AFAP1 60312 actin filament associated protein 1 cytoskeletal protein
AGAP1 116987 "ArfGAP with GTPase domain, ankyrin repeat and PH domain 1" signal transduction autism human accelerated regions
AGC1 176 "aggrecan 1 (chondroitin sulfate proteoglycan 1, large aggregating proteoglycan, antigen identified by monoclonal antibody A0122)" extracellular matrix
AGRN 375790 agrin cell adhesion other neurodegenerative
AGTR1 185 "angiotensin II receptor, type 1" GPCR
AGTR2 186 "angiotensin II receptor, type 2" GPCR mental retardation
AHI1 54806 Abelson helper integration site (Ahi1) other intracellular schizophrenia positive evolution
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
AKR1C2 1646 "aldo-keto reductase family 1, member C2 (dihydrodiol dehydrogenase 2; bile acid binding protein; 3-alpha hydroxysteroid dehydrogenase, type III)" metabolic enzyme obesity layer 6
AKR1C3 8644 "aldo-keto reductase family 1, member C3 (3-alpha hydroxysteroid dehydrogenase, type II)" metabolic enzyme layer 6
AKT1 207 v-akt murine thymoma viral oncogene homolog 1 kinase schizophrenia
ALDH5A1 7915 "aldhehyde dehydrogenase family 5, subfamily A1" metabolic enzyme epilepsy
ALDOC 230 "aldolase C, fructose-bisphosphate" metabolic enzyme
AMMECR1 9949 "Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region, gene 1" other intracellular mental retardation
AMPH 273 amphiphysin (Stiff-Man syndrome with breast cancer 128kDa autoantigen) synaptic protein
ANKHD1 54882 ankyrin repeat and KH domain containing 1 signal transduction schizophrenia
ANKRD34B 340120 ankyrin repeat domain 34B signal transduction
ANXA1 301 annexin A1 signal transduction layer 6
APBA1 320 "amyloid beta (A4) precursor protein- binding, family A, member 1 (X11)" signal transduction Alzheimer’s
APBB2 323 "amyloid beta (A4) precursor protein- binding, family B, member 2 (Fe65- like)" signal transduction Alzheimer’s
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
APLNR 187 apelin receptor GPCR
APLP1 333 amyloid beta (A4) precursor-like protein 1 other membrane protein Alzheimer’s
APLP2 334 amyloid beta (A4) precursor-like protein 2 other membrane protein Alzheimer’s
APOC1 341 apolipoprotein C-I transporter Alzheimer’s
APOL1 8542 "apolipoprotein L, 1" transporter schizophrenia
APOL2 23780 "apolipoprotein L, 2" transporter schizophrenia
APOL4 80832 "apolipoprotein L, 4" transporter schizophrenia
APP 351 "amyloid beta (A4) precursor protein (peptidase nexin-II, Alzheimer’s disease)" other membrane protein Alzheimer’s
ARC 23237 activity-regulated cytoskeleton- associated protein cytoskeletal protein epilepsy
ARFGEF2 10564 ADP-ribosylation factor guanine nucleotide-exchange factor 2 (brefeldin A-inhibited) signal transduction microcephaly microcephaly
ARHGEF10 9639 Rho guanine nucleotide exchange factor (GEF) 10 signal transduction epilepsy
ARHGEF6 9459 Rac/Cdc42 guanine nucleotide exchange factor (GEF) 6 signal transduction mental retardation
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
ARHGEF9 23229 Cdc42 guanine nucleotide exchange factor (GEF) 9 signal transduction mental retardation
ARL4C 10123 ADP-ribosylation factor-like 4C signal transduction
ARNTL2 56938 aryl hydrocarbon receptor nuclear translocator-like 2 transcription factor Hapmap
ASL 435 argininosuccinate lyase metabolic enzyme autism
ASPM 259266 "asp (abnormal spindle) homolog, microcephaly associated (Drosophila)" cytoskeletal protein microcephaly protein evolution; microcephaly
ATBF1 463 AT-binding transcription factor 1 transcription factor human accelerated regions
ATF4 468 activating transcription factor 4 (tax- responsive enhancer element B67) transcription factor schizophrenia
ATF5 22809 activating transcription factor 5 transcription factor schizophrenia
ATF7IP 55729 activating transcription factor 7 interacting protein transcription factor schizophrenia
ATP10A 57194 "ATPase, class V, type 10A" transporter autism
ATP1A2 477 "ATPase, Na+/K+ transporting, alpha 2 (+) polypeptide" transporter epilepsy astrocyte
ATP1A3 478 "ATPase, Na+/K+ transporting, alpha 3 polypeptide" transporter Parkinson’s
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
ATP2A2 488 "ATPase, Ca++ transporting, cardiac muscle, slow twitch 2" transporter epilepsy
ATP2B4 493 "ATPase, Ca++ transporting, plasma membrane 4" transporter layer 2/3/6
ATP6AP2 10159 "ATPase, H+ transporting, lysosomal accessory protein 2" transporter mental retardation
ATP8B1 5205 "ATPase, Class I, type 8B, member 1" transporter positive selection
ATR 545 ataxia telangiectasia and Rad3 related kinase microcephaly microcephaly
ATRX 546 "alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog,
S. cerevisiae)" other nuclear protein mental retardation
AUTS2 26053 autism susceptibility candidate 2 other intracellular autism
AVPR1A 552 arginine vasopressin receptor 1A GPCR autism
AVPR1B 553 arginine vasopressin receptor 1B GPCR depression
AVPR2 554 arginine vasopressin receptor 2 (nephrogenic diabetes insipidus) GPCR
B3GALT2 8707 "UDP-Gal:betaGlcNAc beta 1,3-
galactosyltransferase, polypeptide 2" metabolic enzyme layer 5/6
BACE2 25825 beta-site APP-cleaving enzyme 2 other membrane protein Alzheimer’s
BAD 572 BCL2-antagonist of cell death signal transduction other neurodegenerative
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
BAX 581 BCL2-associated X protein signal transduction other neurodegenerative
BCAN 63827 brevican extracellular matrix astrocyte
BCHE 590 butyrylcholinesterase metabolic enzyme Alzheimer’s
BCL2 596 B-cell CLL/lymphoma 2 signal transduction other neurodegenerative
BCL2L1 598 BCL2-like 1 signal transduction other neurodegenerative
BCL6 604 B-cell CLL/lymphoma 6 (zinc finger protein 51) transcription factor
BCOR 54880 BCL6 co-repressor other nuclear protein mental retardation
BDNF 627 brain-derived neurotrophic factor peptide ligand schizophrenia
BEND5 79656 BEN domain containing 5 other intracellular layer 5
BLMH 642 bleomycin hydrolase metabolic enzyme Alzheimer’s
BRCA1 672 "breast cancer 1, early onset" transcription factor microcephaly
BRD7 29117 bromodomain containing 7 other nuclear protein positive selection
BSN 8927 bassoon (presynaptic cytomatrix protein) synaptic protein other neurodegenerative
BTBD11 121551 BTB (POZ) domain containing 11 other membrane protein interneuron
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
BTN2A1 11120 "butyrophilin, subfamily 2, member A1" other membrane protein positive selection
C11orf87 399947 chromosome 11 open reading frame 87 other membrane protein positive selection
C1QL2 165257 "complement component 1, q subcomponent-like 2" peptide ligand layer 2/3
C20orf103 24141 chromosome 20 open reading frame 103 other membrane protein layer 2/3
C21orf57 54059 Chromosome 21 open reading frame 57 other intracellular "HLS: (IMAGE
clone ID) 50904"
C4orf31 79625 chromosome 4 open reading frame 31 extracellular matrix interneuron/ layer1
C7orf44 55744 chromosome 7 open reading frame 44 other membrane protein positive selection
C8orf59 401466 chromosome 8 open reading frame 59 other intracellular positive selection
C8orf79 57604 chromosome 8 open reading frame 79 other intracellular layer 5
CA2 760 carbonic anhydrase II metabolic enzyme mental retardation microarray expression oligodendrocyte
CA3 761 carbonic anhydrase 3 metabolic enzyme autism
CACNA1B 774 "calcium channel, voltage-dependent, L type, alpha 1B subunit" ion channel pain
CACNA1C 775 "calcium channel, voltage-dependent, L type, alpha 1C subunit" ion channel autism
CACNA1D 776 "calcium channel, voltage-dependent, L type, alpha 1D subunit" ion channel
CACNA1E 777 "calcium channel, voltage-dependent, alpha 1E subunit" ion channel layer 2/3/6
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
CACNA1F 778 "calcium channel, voltage-dependent, alpha 1F subunit" ion channel
CACNA1G 8913 "calcium channel, voltage-dependent, alpha 1G subunit" ion channel
CACNA1I 8911 "calcium channel, voltage-dependent, alpha 1I subunit" ion channel
CACNA1S 779 "calcium channel, voltage-dependent, L type, alpha 1S subunit" ion channel
CACNA2D1 781 "calcium channel, voltage-dependent, alpha 2/delta subunit 1" ion channel
CACNA2D2 9254 "calcium channel, voltage-dependent, alpha 2/delta subunit 2" ion channel interneuron
CACNA2D3 55799 "calcium channel, voltage-dependent, alpha 2/delta 3 subunit" ion channel
CACNA2D4 93589 "calcium channel, voltage-dependent, alpha 2/delta subunit 4" ion channel
CACNB1 782 "calcium channel, voltage-dependent, beta 1 subunit" ion channel epilepsy
CACNB3 784 "calcium channel, voltage-dependent, beta 3 subunit" ion channel
CACNB4 785 "calcium channel, voltage-dependent, beta 4 subunit" ion channel epilepsy
CACNG1 786 "calcium channel, voltage-dependent, gamma subunit 1" ion channel
CACNG2 10369 "calcium channel, voltage-dependent, gamma subunit 2" ion channel
CACNG3 10368 "calcium channel, voltage-dependent, gamma subunit 3" ion channel
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
CACNG4 27092 "calcium channel, voltage-dependent, gamma subunit 4" ion channel
CACNG5 27091 "calcium channel, voltage-dependent, gamma subunit 5" ion channel layer 4c
CACNG6 59285 "calcium channel, voltage-dependent, gamma subunit 6" ion channel
CACNG7 59284 "calcium channel, voltage-dependent, gamma subunit 7" ion channel
CACNG8 59283 "calcium channel, voltage-dependent, gamma subunit 8" ion channel
CADPS2 93664 Ca2+-dependent activator protein for secretion 2 synaptic protein autism
CALB1 793 "calbindin 1, 28kDa" signal transduction interneuron/ layer2
CALB2 794 "calbindin 2, 29kDa (calretinin)" signal transduction interneuron
CALY 50632 calcyon neuron-specific vesicular protein other membrane protein
CAMK2A 815 calcium/calmodulin-dependent protein kinase (CaM kinase) II alpha kinase microarray expression
CAMK4 814 calcium/calmodulin-dependent protein kinase IV kinase
CAMKK2 10645 "calcium/calmodulin-dependent protein kinase kinase 2, beta" kinase
CARTPT 9607 CART prepropeptide peptide ligand obesity layer 2/3
CASP1 834 "caspase 1, apoptosis-related cysteine peptidase (interleukin 1, beta, convertase)" metabolic enzyme other neurodegenerative
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
CASP3 836 "caspase 3, apoptosis-related cysteine peptidase" metabolic enzyme Alzheimer’s protein evolution
CASP7 840 "caspase 7, apoptosis-related cysteine peptidase" metabolic enzyme other neurodegenerative
CASP8 841 "caspase 8, apoptosis-related cysteine peptidase" metabolic enzyme other neurodegenerative
CBLN2 147381 cerebellin 2 precursor other membrane protein layer 2/3/6
CC2D1A 54862 coiled-coil and C2 domain containing 1A transcription factor mental retardation
CCDC141 285025 coiled-coil domain containing 141 cytoskeletal protein schizophrenia
CCK 885 cholecystokinin peptide ligand anxiety layer 2/3/5/6
CCKAR 886 cholecystokinin A receptor GPCR
CCKBR 887 cholecystokinin B receptor GPCR
CDH13 1012 "cadherin 13, H-cadherin (heart)" cell adhesion interneuron/ layer2
CDH24 64403 cadherin-like 24 cell adhesion layer 6
CDH7 1005 "cadherin 7, type 2" cell adhesion interneuron
CDK5 1020 cyclin-dependent kinase 5 kinase other neurodegenerative
CDK5R1 8851 "cyclin-dependent kinase 5, regulatory subunit 1 (p35)" signal transduction other neurodegenerative
CDK5R2 8941 "cyclin-dependent kinase 5, regulatory subunit 2 (p39)" signal transduction other neurodegenerative
CDK5RAP1 51654 CDK5 regulatory subunit associated protein 1 signal transduction
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
CDK5RAP2 55755 CDK5 regulatory subunit associated protein 2 signal transduction microcephaly microcephaly
CDK5RAP3 80279 CDK5 regulatory subunit associated protein 3 signal transduction
CDKL5 6792 cyclin-dependent kinase-like 5 kinase epilepsy
CENPJ 55835 centromere protein J cytoskeletal protein microcephaly microcephaly
CEP290 80184 centrosomal protein 290kDa other nuclear protein autism
CERK 64781 ceramide kinase kinase interneuron
CFC1 55997 "Cripto, FRL-1, cryptic family 1" signal transduction "HLS: (IMAGE
clone ID) 328821"
CFTR 1080 "cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)" transporter
CHEK1 1111 CHK1 checkpoint homolog (S. pombe) kinase microcephaly
CHRM1 1128 "cholinergic receptor, muscarinic 1" GPCR schizophrenia
CHRM2 1129 "cholinergic receptor, muscarinic 2" GPCR depression
CHRM3 1131 "cholinergic receptor, muscarinic 3" GPCR
CHRM4 1132 "cholinergic receptor, muscarinic 4" GPCR
CHRM5 1133 "cholinergic receptor, muscarinic 5" GPCR protein evolution
CHRNA10 57053 "cholinergic receptor, nicotinic, alpha 10" ion channel
CHRNA3 1136 "cholinergic receptor, nicotinic, alpha 3" ion channel Alzheimer’s layer 4c
CHRNA4 1137 "cholinergic receptor, nicotinic, alpha 4" ion channel epilepsy layer 5/6
CHRNA5 1138 "cholinergic receptor, nicotinic, alpha 5" ion channel protein evolution
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
CHRNA6 8973 "cholinergic receptor, nicotinic, alpha 6" ion channel
CHRNA7 1139 "cholinergic receptor, nicotinic, alpha 7" ion channel schizophrenia layer 1/2
CHRNA9 55584 "cholinergic receptor, nicotinic, alpha 9" ion channel
CHRNB2 1141 "cholinergic receptor, nicotinic, beta 2 (neuronal)" ion channel epilepsy
CHRNB3 1142 "cholinergic receptor, nicotinic, beta 3" ion channel
CHRNB4 1143 "cholinergic receptor, nicotinic, beta 4" ion channel
CHRND 1144 "cholinergic receptor, nicotinic, delta" ion channel
CHRNE 1145 "cholinergic receptor, nicotinic, epsilon" ion channel
CHRNG 1146 "cholinergic receptor, nicotinic, gamma" ion channel
CIT 11113 "citron (rho-interacting, serine/threonine kinase 21)" kinase schizophrenia
CLCA1 1179 "chloride channel, calcium activated, family member 1" ion channel positive selection
CLCA2 9635 "chloride channel, calcium activated, family member 2" ion channel
CLCA3 9629 "chloride channel, calcium activated, family member 3" ion channel
CLCA4 22802 "chloride channel, calcium activated, family member 4" ion channel positive selection
CLCN1 1180 "chloride channel 1, skeletal muscle (Thomsen disease, autosomal dominant)" ion channel
CLCN2 1181 chloride channel 2 ion channel epilepsy
CLCN3 1182 chloride channel 3 ion channel
CLCN4 1183 chloride channel 4 ion channel
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
CLCN5 1184 "chloride channel 5 (nephrolithiasis 2, X-linked, Dent disease)" ion channel
CLCN6 1185 chloride channel 6 ion channel
CLCN7 1186 chloride channel 7 ion channel
CLCNKA 1187 chloride channel Ka ion channel
CLCNKB 1188 chloride channel Kb ion channel
CLDN5 7122 claudin 5 (transmembrane protein deleted in velocardiofacial syndrome) other membrane protein VEC
CLIC1 1192 chloride intracellular channel 1 ion channel
CLIC2 1193 chloride intracellular channel 2 ion channel
CLIC3 9022 chloride intracellular channel 3 ion channel
CLIC4 25932 chloride intracellular channel 4 ion channel
CLIC5 53405 chloride intracellular channel 5 ion channel
CLIC6 54102 chloride intracellular channel 6 ion channel
CLN8 2055 "ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)" other membrane protein epilepsy
CLNS1A 1207 "chloride channel, nucleotide-sensitive, 1A" ion channel
CLOCK 9575 clock homolog (mouse) transcription factor bipolar
CNGA1 1259 cyclic nucleotide gated channel alpha 1 ion channel
CNGA2 1260 cyclic nucleotide gated channel alpha 2 ion channel
CNGA4 1262 cyclic nucleotide gated channel alpha 4 ion channel
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
CNGB3 54714 cyclic nucleotide gated channel beta 3 ion channel
CNP 1267 "2',3'-cyclic nucleotide 3' phosphodiesterase" metabolic enzyme oligodendrocyte
CNR1 1268 cannabinoid receptor 1 (brain) GPCR depression interneuron/ layer1/2/6
CNTNAP2 26047 contactin associated protein-like 2 cell adhesion epilepsy frontal cortex expression
CNTNAP4 85445 contactin associated protein-like 4 cell adhesion interneuron+ laminar
COL12A1 1303 "collagen, type XII, alpha 1" extracellular matrix
COL24A1 255631 "collagen, type XXIV, alpha 1" extracellular matrix layer 2/3/5/6
COL5A1 1289 "collagen, type V, alpha 1" extracellular matrix
COL6A1 1291 "collagen, type VI, alpha 1" extracellular matrix microarray expression layer 3/4/5/6
COL9A3 1299 "collagen, type IX, alpha 3" extracellular matrix interneuron
COMT 1312 catechol-O-methyltransferase metabolic enzyme schizophrenia
CORT 1325 cortistatin peptide ligand interneuron
COX6A2 1339 cytochrome c oxidase subunit VIa polypeptide 2 metabolic enzyme
COX8A 1351 cytochrome c oxidase subunit 8A (ubiquitous) metabolic enzyme energy demand
CPLX3 594855 complexin 3 synaptic protein interneuron
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
CPNE7 27132 copine VII signal transduction interneuron/ layer5/6
CPOX 1371 coproporphyrinogen oxidase metabolic enzyme positive selection
CRBN 51185 cereblon other intracellular mental retardation
CREB1 1385 cAMP responsive element binding protein 1 transcription factor depression
CRH 1392 corticotropin releasing hormone peptide ligand depression
CRHBP 1393 corticotropin releasing hormone binding protein secreted protein interneuron
CRHR1 1394 corticotropin releasing hormone receptor 1 GPCR depression
CRHR2 1395 corticotropin releasing hormone receptor 2 GPCR depression
CRYM 1428 "crystallin, mu" other intracellular layer 2/3/5/6
CSMD1 64478 CUB and Sushi multiple domains 1 other membrane protein CNV
CSNK1D 1453 "casein kinase 1, delta" kinase other neurodegenerative
CSPG3 1463 chondroitin sulfate proteoglycan 3 (neurocan) extracellular matrix protein evolution
CSRP1 1465 cysteine and glycine-rich protein 1 other nuclear protein oligodendrocyte
CST3 1471 cystatin C (amyloid angiopathy and cerebral hemorrhage) secreted protein epilepsy astrocyte
CSTB 1476 cystatin B (stefin B) other intracellular epilepsy
CTGF 1490 connective tissue growth factor peptide ligand layer 6b
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
CTNNB1 1499 "catenin (cadherin-associated protein), beta 1, 88kDa" cell adhesion
CTNND2 1501 "catenin (cadherin-associated protein), delta 2 (neural plakophilin-related arm- repeat protein)" cell adhesion mental retardation
CTSB 1508 cathepsin B metabolic enzyme Alzheimer’s
CUX1 1523 cut-like homeobox 1 transcription factor
CUX2 23316 cut-like homeobox 2 transcription factor depression Hapmap layer 2/3/4
CXCL12 6387 chemokine (C-X-C motif) ligand 12 (stromal cell-derived factor 1) peptide ligand
CXCL14 9547 chemokine (C-X-C motif) ligand 14 peptide ligand interneuron/ layer1
CYP26B1 56603 "cytochrome P450, family 26, subfamily B, polypeptide 1" metabolic enzyme
CYP39A1 51302 "cytochrome P450, family 39, subfamily A, polypeptide 1" metabolic enzyme
CYR61 3491 "cysteine-rich, angiogenic inducer, 61" secreted protein layer 6
DAO 1610 D-amino-acid oxidase metabolic enzyme schizophrenia
DAOA 267012 D-amino acid oxidase activator other intracellular schizophrenia
DBH 1621 dopamine beta-hydroxylase (dopamine beta-monooxygenase) metabolic enzyme Parkinson’s
DBN1 1627 drebrin 1 cytoskeletal protein Alzheimer’s
DCX 1641 "doublecortex; lissencephaly, X-linked (doublecortin)" cytoskeletal protein mental retardation
DDC 1644 dopa decarboxylase metabolic enzyme Parkinson’s
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
DDIT4L 115265 DNA-damage-inducible transcript 4- like signal transduction
DDT 1652 D-dopachrome tautomerase metabolic enzyme
DDX11 1663 "DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 11 (CHL1-like helicase homolog, S. cerevisiae)" other nuclear protein "HLS: (IMAGE
clone ID) 470930"
DECR1 1666 "2,4-dienoyl CoA reductase 1, mitochondrial" metabolic enzyme
DEPDC6 64798 DEP domain containing 6 signal transduction
DFNB31 25861 "deafness, autosomal recessive 31" cytoskeletal protein deafness
DHCR7 1717 7-dehydrocholesterol reductase metabolic enzyme autism
DHX9 1660 DEAH (Asp-Glu-Ala-His) box polypeptide 9 other nuclear protein positive selection
DISC1 27185 disrupted in schizophrenia 1 signal transduction schizophrenia layer 1
DKC1 1736 "dyskeratosis congenita 1, dyskerin" other nuclear protein microcephaly
DKK3 27122 dickkopf homolog 3 (Xenopus laevis) secreted protein
DLEC1 9940 deleted in lung and esophageal cancer 1 other intracellular positive selection
DLG1 1739 "discs, large homolog 1 (Drosophila)" synaptic protein
DLG2 1740 "discs, large homolog 2, chapsyn-110 (Drosophila)" synaptic protein
DLG3 1741 "discs, large homolog 3 (neuroendocrine-dlg, Drosophila)" synaptic protein mental retardation
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
DLG4 1742 "discs, large homolog 4 (Drosophila)" synaptic protein
DLG5 9231 "discs, large homolog 5 (Drosophila)" synaptic protein
DLGAP1 9229 "discs, large (Drosophila) homolog- associated protein 1" synaptic protein
DLGAP2 9228 "discs, large (Drosophila) homolog- associated protein 2" synaptic protein
DLX1 1745 distal-less homeobox 1 transcription factor autism interneuron
DLX5 1749 distal-less homeobox 5 transcription factor autism
DPP6 1804 dipeptidyl-peptidase 6 other membrane protein protein evolution
DRD1 1812 dopamine receptor D1 GPCR schizophrenia
DRD3 1814 dopamine receptor D3 GPCR schizophrenia
DRD5 1816 dopamine receptor D5 GPCR schizophrenia
DSG1 1828 desmoglein 1 cell adhesion positive selection
DTNA 1837 "dystrobrevin, alpha" synaptic protein
DTNBP1 84062 dystrobrevin binding protein 1 synaptic protein schizophrenia
DVL1 1855 "dishevelled, dsh homolog 1 (Drosophila)" signal transduction autism protein evolution
DYM 54808 dymeclin other intracellular microcephaly
DYNC1I2 1781 "Dynein, cytoplasmic 1, intermediate chain 2" cytoskeletal protein "HLS: (IMAGE
clone ID) 809714"
DYX1C1 161582 dyslexia susceptibility 1 candidate 1 other nuclear protein
ECE2 9718 endothelin converting enzyme 2 metabolic enzyme interneuron
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
EDNRA 1909 endothelin receptor type A GPCR
EDNRB 1910 endothelin receptor type B GPCR deafness
EN2 2020 engrailed homeobox 2 transcription factor autism
ENC1 8507 ectodermal-neural cortex (with BTB- like domain) cytoskeletal protein layer 2/3/5/6
ENDOD1 23052 endonuclease domain containing 1 secreted protein
EPHA6 285220 EPH receptor A6 kinase layer 2
ERBB3 2065 v-erb-b2 erythroblastic leukemia viral oncogene homolog 3 (avian) kinase schizophrenia
ERBB4 2066 v-erb-a erythroblastic leukemia viral oncogene homolog 4 (avian) kinase schizophrenia interneuron
ERCC2 2068 "excision repair cross-complementing rodent repair deficiency, complementation group 2 (xeroderma pigmentosum D)" other nuclear protein microcephaly
ERCC3 2071 "excision repair cross-complementing rodent repair deficiency, complementation group 3 (xeroderma pigmentosum group B complementing)" other nuclear protein microcephaly
ERCC5 2073 "excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G (Cockayne syndrome))" other nuclear protein microcephaly
ESCO2 157570 establishment of cohesion 1 homolog 2 (S. cerevisiae) other nuclear protein microcephaly
ESR1 2099 estrogen receptor 1 transcription factor Alzheimer’s
ESR2 2100 estrogen receptor 2 (ER beta) transcription factor
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
ETV1 2115 ets variant gene 1 transcription factor layer 5
EXT1 2131 exostoses (multiple) 1 metabolic enzyme autism
EYA4 2070 eyes absent homolog 4 (Drosophila) other nuclear protein deafness hearing interneuron
FABP7 2173 fatty acid binding protein 7 other intracellular
FAM111A 63901 "family with sequence similarity 111, member A" other intracellular positive selection
FAM111B 374393 "family with sequence similarity 111, member B" other intracellular positive selection
FAM20A 54757 "family with sequence similarity 20, member A" secreted protein
FAM3C 10447 "family with sequence similarity 3, member C" secreted protein layer 5
FAM46A 55603 "family with sequence similarity 46, member A" interneuron
FEZ1 9638 fasciculation and elongation protein zeta 1 (zygin I) signal transduction schizophrenia
FGD1 2245 "FYVE, RhoGEF and PH domain containing 1 (faciogenital dysplasia)" signal transduction mental retardation
FGF1 2246 fibroblast growth factor 1 (acidic) peptide ligand
FGF14 2259 fibroblast growth factor 14 peptide ligand other neurodegenerative
FGF2 2247 fibroblast growth factor 2 (basic) peptide ligand other neurodegenerative
FGF9 2254 fibroblast growth factor 9 (glia- activating factor) peptide ligand
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
FGFR1 2260 "fibroblast growth factor receptor 1 (fms-related tyrosine kinase 2, Pfeiffer syndrome)" kinase mental retardation
FGFR2 2263 "fibroblast growth factor receptor 2 (bacteria-expressed kinase, keratinocyte growth factor receptor, craniofacial dysostosis 1, Crouzon syndrome, Pfeiffer syndrome, Jackson-Weiss syndrome)" kinase
FMR1 2332 fragile X mental retardation 1 other intracellular mental retardation
FOXP2 93986 forkhead box P2 transcription factor autism positive evolution layer 6
FRA10AC1 118924 chromosome 10 open reading frame 4 other nuclear protein positive selection
FST 10468 follistatin secreted protein
FTSJ1 24140 FtsJ homolog 1 (E. coli) other nuclear protein mental retardation
FXYD6 53826 FXYD domain containing ion transport regulator 6 other membrane protein layer 2/3/5/6
FYN 2534 Fyn proto-oncogene kinase
GABARAP 11337 GABA(A) receptor-associated protein synaptic protein
GABARAPL1 23710 GABA(A) receptor-associated protein like 1 synaptic protein
GABARAPL2 11345 GABA(A) receptor-associated protein- like 2 synaptic protein
GABBR1 2550 "gamma-aminobutyric acid (GABA) B receptor, 1" GPCR epilepsy
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
GABBR2 9568 "gamma-aminobutyric acid (GABA) B receptor, 2" GPCR epilepsy
GABRA1 2554 "gamma-aminobutyric acid (GABA) A receptor, alpha 1" ion channel epilepsy
GABRA2 2555 "gamma-aminobutyric acid (GABA) A receptor, alpha 2" ion channel autism
GABRA3 2556 "gamma-aminobutyric acid (GABA) A receptor, alpha 3" ion channel
GABRA4 2557 "gamma-aminobutyric acid (GABA) A receptor, alpha 4" ion channel autism
GABRA5 2558 "gamma-aminobutyric acid (GABA) A receptor, alpha 5" ion channel autism layer 5/6
GABRA6 2559 "gamma-aminobutyric acid (GABA) A receptor, alpha 6" ion channel schizophrenia
GABRB1 2560 "gamma-aminobutyric acid (GABA) A receptor, beta 1" ion channel autism
GABRB2 2561 "gamma-aminobutyric acid (GABA) A receptor, beta 2" ion channel schizophrenia
GABRB3 2562 "gamma-aminobutyric acid (GABA) A receptor, beta 3" ion channel epilepsy
GABRD 2563 "gamma-aminobutyric acid (GABA) A receptor, delta" ion channel
GABRE 2564 "gamma-aminobutyric acid (GABA) A receptor, epsilon" ion channel epilepsy
GABRG1 2565 "gamma-aminobutyric acid (GABA) A receptor, gamma 1" ion channel autism
GABRG2 2566 "gamma-aminobutyric acid (GABA) A receptor, gamma 2" ion channel epilepsy
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
GABRG3 2567 "gamma-aminobutyric acid (GABA) A receptor, gamma 3" ion channel autism
GABRP 2568 "gamma-aminobutyric acid (GABA) A receptor, pi" ion channel
GABRQ 55879 "gamma-aminobutyric acid (GABA) receptor, theta" ion channel
GABRR1 2569 "gamma-aminobutyric acid (GABA) receptor, rho 1" ion channel
GABRR2 2570 "gamma-aminobutyric acid (GABA) receptor, rho 2" ion channel
GABRR3 200959 "gamma-aminobutyric acid (GABA) receptor, rho 3" ion channel
GAD1 2571 "glutamate decarboxylase 1 (brain, 67kDa)" metabolic enzyme schizophrenia interneuron
GAD2 2572 "glutamate decarboxylase 2 (pancreatic islets and brain, 65kDa)" metabolic enzyme depression interneuron
GALR2 8811 galanin receptor 2 GPCR
GAP43 2596 growth associated protein 43 synaptic protein epilepsy
GDI1 2664 GDP dissociation inhibitor 1 signal transduction mental retardation protein evolution
GFAP 2670 glial fibrillary acidic protein cytoskeletal protein other neurodegenerative astrocyte
GIPR 2696 gastric inhibitory polypeptide receptor GPCR
GJA1 2697 "gap junction protein, alpha 1, 43kDa (connexin 43)" other membrane protein microcephaly astrocyte
GLO1 2739 glyoxalase 1 metabolic enzyme autism CNV
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
GLRA1 2741 "glycine receptor, alpha 1 (startle disease/hyperekplexia, stiff man syndrome)" ion channel
GLRA2 2742 "glycine receptor, alpha 2" ion channel autism
GLRA3 8001 "glycine receptor, alpha 3" ion channel autism layer 2
GLRB 2743 "glycine receptor, beta" ion channel autism
GLUD2 2747 glutamate dehydrogenase 2 metabolic enzyme brain evolution
GM2A 2760 GM2 ganglioside activator metabolic enzyme microarray expression
GMPR 2766 guanosine monophosphate reductase metabolic enzyme
GNB4 59345 "guanine nucleotide binding protein (G protein), beta polypeptide 4" signal transduction
GNG7 2788 "guanine nucleotide binding protein (G protein), gamma 7" signal transduction
GNRHR 2798 gonadotropin-releasing hormone receptor GPCR
GOSR1 9527 golgi SNAP receptor complex member 1 synaptic protein microarray expression
GPHN 10243 gephyrin synaptic protein
GPR101 83550 G protein-coupled receptor 101 GPCR
GPR116 221395 G protein-coupled receptor 116 GPCR "HLS: (IMAGE
clone ID)307337"
GPR12 2835 G protein-coupled receptor 12 GPCR
GPR156 165829 G protein-coupled receptor 156 GPCR
GPR161 23432 G protein-coupled receptor 161 GPCR
GPR173 54328 G protein-coupled receptor 173 GPCR
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
GPR176 11245 G protein-coupled receptor 176 GPCR
GPR19 2842 G protein-coupled receptor 19 GPCR
GPR22 2845 G protein-coupled receptor 22 GPCR
GPR3 2827 G protein-coupled receptor 3 GPCR
GPR37 2861 G protein-coupled receptor 37 (endothelin receptor type B-like) GPCR
GPR50 9248 G protein-coupled receptor 50 GPCR depression
GPR56 9289 G protein-coupled receptor 56 GPCR
GPR6 2830 G protein-coupled receptor 6 GPCR
GPR78 27201 G protein-coupled receptor 78 GPCR
GPR83 10888 G protein-coupled receptor 83 GPCR
GPR85 54329 G protein-coupled receptor 85 GPCR
GPR88 54112 G protein-coupled receptor 88 GPCR
GPR98 84059 G protein-coupled receptor 98 GPCR epilepsy
GPRIN3 285513 GPRIN family member 3 signal transduction
GRB2 2885 growth factor receptor-bound protein 2 signal transduction other neurodegenerative "HLS: (IMAGE
clone ID)384872"
GRIA1 2890 "glutamate receptor, ionotropic, AMPA 1" ion channel epilepsy
GRIA2 2891 "glutamate receptor, ionotropic, AMPA 2" ion channel epilepsy
GRIA3 2892 "glutamate receptor, ionotrophic, AMPA 3" ion channel epilepsy
GRIA4 2893 "glutamate receptor, ionotrophic, AMPA 4" ion channel
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
GRID1 2894 "glutamate receptor, ionotropic, delta 1" ion channel
GRID2 2895 "glutamate receptor, ionotropic, delta 2" ion channel
GRIK1 2897 "glutamate receptor, ionotropic, kainate 1" ion channel epilepsy interneuron
GRIK2 2898 "glutamate receptor, ionotropic, kainate 2" ion channel mental retardation
GRIK3 2899 "glutamate receptor, ionotropic, kainate 3" ion channel
GRIK4 2900 "glutamate receptor, ionotropic, kainate 4" ion channel protein evolution layer 4c/6
GRIK5 2901 "glutamate receptor, ionotropic, kainate 5" ion channel
GRIN1 2902 "glutamate receptor, ionotropic, N- methyl D-aspartate 1" ion channel schizophrenia
GRIN2A 2903 "glutamate receptor, ionotropic, N- methyl D-aspartate 2A" ion channel schizophrenia protein evolution
GRIN2B 2904 "glutamate receptor, ionotropic, N- methyl D-aspartate 2B" ion channel schizophrenia
GRIN2C 2905 "glutamate receptor, ionotropic, N- methyl D-aspartate 2C" ion channel
GRIN2D 2906 "glutamate receptor, ionotropic, N- methyl D-aspartate 2D" ion channel
GRIN3A 116443 "glutamate receptor, ionotropic, N- methyl-D-aspartate 3A" ion channel interneuron/ layer5/6
GRIN3B 116444 "glutamate receptor, ionotropic, N- methyl-D-aspartate 3B" ion channel
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
GRINA 2907 "glutamate receptor, ionotropic, N- methyl D-asparate-associated protein 1 (glutamate binding)" ion channel
GRINL1A 81488 "glutamate receptor, ionotropic, N- methyl D-aspartate-like 1A" other nuclear protein
GRIP1 23426 glutamate receptor interacting protein 1 synaptic protein
GRIP2 80852 glutamate receptor interacting protein 2 synaptic protein
GRM1 2911 "glutamate receptor, metabotropic 1" GPCR epilepsy
GRM2 2912 "glutamate receptor, metabotropic 2" GPCR schizophrenia
GRM3 2913 "glutamate receptor, metabotropic 3" GPCR schizophrenia
GRM4 2914 "glutamate receptor, metabotropic 4" GPCR epilepsy
GRM6 2916 "glutamate receptor, metabotropic 6 (GluR6)" GPCR
GRM7 2917 "glutamate receptor, metabotropic 7" GPCR schizophrenia
GRM8 2918 "glutamate receptor, metabotropic 8" GPCR autism
GRPR 2925 gastrin releasing peptide receptor GPCR autism
GSG1L 146395 GSG1-like other membrane protein layer 2/3
GSK3B 2932 glycogen synthase kinase 3 beta kinase Alzheimer’s
GSN 2934 "gelsolin (amyloidosis, Finnish type)" cytoskeletal protein oligodendrocyte
GTF2H2C 728340 "general transcription factor IIH, polypeptide 2C" transcription factor "HLS: (IMAGE
clone ID) 712622"
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
GTF2I 2969 "general transcription factor II, i" transcription factor microarray expression
GXYLT2 727936 glucoside xylosyltransferase 2 extracellular matrix
HAPLN1 1404 hyaluronan and proteoglycan link protein 1 extracellular matrix
HBD 3045 "hemoglobin, delta" other intracellular VEC
HCN1 348980 hyperpolarization activated cyclic nucleotide-gated potassium channel 1 ion channel
HCN2 610 hyperpolarization activated cyclic nucleotide-gated potassium channel 2 ion channel
HCN3 57657 hyperpolarization activated cyclic nucleotide-gated potassium channel 3 ion channel
HCN4 10021 hyperpolarization activated cyclic nucleotide-gated potassium channel 4 ion channel
HCRTR1 3061 hypocretin (orexin) receptor 1 GPCR
HCRTR2 3062 hypocretin (orexin) receptor 2 GPCR
HOMER1 9456 homer homolog 1 (Drosophila) synaptic protein schizophrenia microarray expression
HPSE 10855 heparanase extracellular matrix interneuron
HRH1 3269 histamine receptor H1 GPCR
HRH4 59340 histamine receptor H4 GPCR
HSD11B1 3290 hydroxysteroid (11-beta) dehydrogenase 1 metabolic enzyme
HSPG2 3339 heparan sulfate proteoglycan 2 (perlecan) extracellular matrix
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
HTR1A 3350 5-hydroxytryptamine (serotonin) receptor 1A GPCR depression
HTR1B 3351 5-hydroxytryptamine (serotonin) receptor 1B GPCR depression
HTR1D 3352 5-hydroxytryptamine (serotonin) receptor 1D GPCR depression
HTR1E 3354 5-hydroxytryptamine (serotonin) receptor 1E GPCR
HTR1F 3355 5-hydroxytryptamine (serotonin) receptor 1F GPCR
HTR2A 3356 5-hydroxytryptamine (serotonin) receptor 2A GPCR schizophrenia
HTR2B 3357 5-hydroxytryptamine (serotonin) receptor 2B GPCR
HTR2C 3358 5-hydroxytryptamine (serotonin) receptor 2C GPCR schizophrenia layer 5
HTR3A 3359 5-hydroxytryptamine (serotonin) receptor 3A ion channel depression
HTR4 3360 5-hydroxytryptamine (serotonin) receptor 4 GPCR
HTR5A 3361 5-hydroxytryptamine (serotonin) receptor 5A GPCR depression
HTR6 3362 5-hydroxytryptamine (serotonin) receptor 6 GPCR schizophrenia
HTR7 3363 5-hydroxytryptamine (serotonin) receptor 7 (adenylate cyclase-coupled) GPCR autism
HTRA2 27429 HtrA serine peptidase 2 metabolic enzyme Parkinson’s
ID2 3398 inhibitor of DNA binding 2 transcription factor
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
IGBP1 3476 immunoglobulin (CD79A) binding protein 1 signal transduction mental retardation
IGF1 3479 insulin-like growth factor 1 (somatomedin C) peptide ligand mental retardation
IGFBP4 3487 insulin-like growth factor binding protein 4 secreted protein
IGFN1 91156 immunoglobulin-like and fibronectin type III domain containing 1 cell adhesion
IGSF11 152404 "immunoglobulin superfamily, member 11" cell adhesion layer 2/3
IGSF21 84966 "immunoglobin superfamily, member 21" secreted protein
IL1B 3553 "interleukin 1, beta" peptide ligand Alzheimer’s
IL1RAPL1 11141 interleukin 1 receptor accessory protein-like 1 other membrane protein mental retardation
INPP1 3628 inositol polyphosphate-1-phosphatase signal transduction autism
INPP4B 8821 "inositol polyphosphate-4-phosphatase, type II, 105kDa" signal transduction
INSR 3643 insulin receptor kinase other neurodegenerative
ITGA5 3678 "integrin, alpha 5 (fibronectin receptor, alpha polypeptide)" cell adhesion
ITPR2 3709 "inositol 1,4,5-triphosphate receptor, type 2" ion channel
ITSN1 6453 intersectin 1 (SH3 domain protein) signal transduction schizophrenia
JRK 8629 jerky homolog (mouse) other nuclear protein epilepsy
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
KCNA1 3736 "potassium voltage-gated channel, shaker-related subfamily, member 1 (episodic ataxia with myokymia)" ion channel epilepsy layer 3/5/6
KCNA10 3744 "potassium voltage-gated channel, shaker-related subfamily, member 10" ion channel
KCNA2 3737 "potassium voltage-gated channel, shaker-related subfamily, member 2" ion channel
KCNA3 3738 "potassium voltage-gated channel, shaker-related subfamily, member 3" ion channel
KCNA4 3739 "potassium voltage-gated channel, shaker-related subfamily, member 4" ion channel
KCNA5 3741 "potassium voltage-gated channel, shaker-related subfamily, member 5" ion channel
KCNA6 3742 "potassium voltage-gated channel, shaker-related subfamily, member 6" ion channel
KCNA7 3743 "potassium voltage-gated channel, shaker-related subfamily, member 7" ion channel
KCNAB1 7881 "potassium voltage-gated channel, shaker-related subfamily, beta member 1" ion channel interneuron
KCNAB2 8514 "potassium voltage-gated channel, shaker-related subfamily, beta member 2" ion channel
KCNAB3 9196 "potassium voltage-gated channel, shaker-related subfamily, beta member 3" ion channel
KCNB1 3745 "potassium voltage-gated channel, Shab-related subfamily, member 1" ion channel
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
KCNB2 9312 "potassium voltage-gated channel, Shab-related subfamily, member 2" ion channel
KCNC1 3746 "potassium voltage-gated channel, Shaw-related subfamily, member 1" ion channel
KCNC2 3747 "potassium voltage-gated channel, Shaw-related subfamily, member 2" ion channel interneuron
KCNC3 3748 "potassium voltage-gated channel, Shaw-related subfamily, member 3" ion channel
KCNC4 3749 "potassium voltage-gated channel, Shaw-related subfamily, member 4" ion channel
KCND1 3750 "potassium voltage-gated channel, Shal-related subfamily, member 1" ion channel
KCND2 3751 "potassium voltage-gated channel, Shal-related subfamily, member 2" ion channel
KCND3 3752 "potassium voltage-gated channel, Shal-related subfamily, member 3" ion channel
KCNE1 3753 "potassium voltage-gated channel, Isk- related family, member 1" ion channel
KCNE2 9992 "potassium voltage-gated channel, Isk- related family, member 2" ion channel
KCNE3 10008 "potassium voltage-gated channel, Isk- related family, member 3" ion channel
KCNE4 23704 "potassium voltage-gated channel, Isk- related family, member 4" ion channel
KCNF1 3754 "potassium voltage-gated channel, subfamily F, member 1" ion channel
KCNG3 170850 "potassium voltage-gated channel, subfamily G, member 3" ion channel
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
KCNG4 93107 "potassium voltage-gated channel, subfamily G, member 4" ion channel
KCNH1 3756 "potassium voltage-gated channel, subfamily H (eag-related), member 1" ion channel
KCNH2 3757 "potassium voltage-gated channel, subfamily H (eag-related), member 2" ion channel
KCNH3 23416 "potassium voltage-gated channel, subfamily H (eag-related), member 3" ion channel
KCNH4 23415 "potassium voltage-gated channel, subfamily H (eag-related), member 4" ion channel layer 2/3/6
KCNH5 27133 "potassium voltage-gated channel, subfamily H (eag-related), member 5" ion channel
KCNH6 81033 "potassium voltage-gated channel, subfamily H (eag-related), member 6" ion channel epilepsy
KCNH7 90134 "potassium voltage-gated channel, subfamily H (eag-related), member 7" ion channel
KCNH8 131096 "potassium voltage-gated channel, subfamily H (eag-related), member 8" ion channel
KCNIP1 30820 Kv channel interacting protein 1 signal transduction interneuron
KCNIP2 30819 Kv channel interacting protein 2 signal transduction interneuron/ layer2/3
KCNIP3 30818 "Kv channel interacting protein 3, calsenilin" signal transduction Alzheimer’s
KCNJ1 3758 "potassium inwardly-rectifying channel, subfamily J, member 1" ion channel
KCNJ10 3766 "potassium inwardly-rectifying channel, subfamily J, member 10" ion channel epilepsy
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
KCNJ11 3767 "potassium inwardly-rectifying channel, subfamily J, member 11" ion channel
KCNJ12 3768 "potassium inwardly-rectifying channel, subfamily J, member 12" ion channel
KCNJ13 3769 "potassium inwardly-rectifying channel, subfamily J, member 13" ion channel
KCNJ14 3770 "potassium inwardly-rectifying channel, subfamily J, member 14" ion channel
KCNJ15 3772 "potassium inwardly-rectifying channel, subfamily J, member 15" ion channel
KCNJ16 3773 "potassium inwardly-rectifying channel, subfamily J, member 16" ion channel
KCNJ2 3759 "potassium inwardly-rectifying channel, subfamily J, member 2" ion channel
KCNJ3 3760 "potassium inwardly-rectifying channel, subfamily J, member 3" ion channel epilepsy
KCNJ4 3761 "potassium inwardly-rectifying channel, subfamily J, member 4" ion channel
KCNJ5 3762 "potassium inwardly-rectifying channel, subfamily J, member 5" ion channel
KCNJ6 3763 "potassium inwardly-rectifying channel, subfamily J, member 6" ion channel epilepsy
KCNJ8 3764 "potassium inwardly-rectifying channel, subfamily J, member 8" ion channel
KCNK1 3775 "potassium channel, subfamily K, member 1" ion channel
KCNK10 54207 "potassium channel, subfamily K, member 10" ion channel
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
KCNK13 56659 "potassium channel, subfamily K, member 13" ion channel
KCNK15 60598 "potassium channel, subfamily K, member 15" ion channel
KCNK16 83795 "potassium channel, subfamily K, member 16" ion channel
KCNK17 89822 "potassium channel, subfamily K, member 17" ion channel
KCNK18 338567 "potassium channel, subfamily K, member 18" ion channel
KCNK2 3776 "potassium channel, subfamily K, member 2" ion channel layer 5/6
KCNK3 3777 "potassium channel, subfamily K, member 3" ion channel
KCNK4 50801 "potassium channel, subfamily K, member 4" ion channel
KCNK5 8645 "potassium channel, subfamily K, member 5" ion channel
KCNK6 9424 "potassium channel, subfamily K, member 6" ion channel
KCNK7 10089 "potassium channel, subfamily K, member 7" ion channel
KCNK9 51305 "potassium channel, subfamily K, member 9" ion channel epilepsy
KCNMB1 3779 "potassium large conductance calcium- activated channel, subfamily M, beta member 1" ion channel
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
KCNMB2 10242 "potassium large conductance calcium- activated channel, subfamily M, beta member 2" ion channel
KCNMB3 27094 "potassium large conductance calcium- activated channel, subfamily M beta member 3" ion channel
KCNMB4 27345 "potassium large conductance calcium- activated channel, subfamily M, beta member 4" ion channel
KCNN1 3780 "potassium intermediate/small conductance calcium-activated channel, subfamily N, member 1" ion channel
KCNN2 3781 "potassium intermediate/small conductance calcium-activated channel, subfamily N, member 2" ion channel
KCNN3 3782 "potassium intermediate/small conductance calcium-activated channel, subfamily N, member 3" ion channel schizophrenia
KCNN4 3783 "potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4" ion channel
KCNQ1 3784 "potassium voltage-gated channel, KQT-like subfamily, member 1" ion channel
KCNQ2 3785 "potassium voltage-gated channel, KQT-like subfamily, member 2" ion channel epilepsy
KCNQ3 3786 "potassium voltage-gated channel, KQT-like subfamily, member 3" ion channel epilepsy
KCNQ4 9132 "potassium voltage-gated channel, KQT-like subfamily, member 4" ion channel
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
KCNQ5 56479 "potassium voltage-gated channel, KQT-like subfamily, member 5" ion channel
KCNS2 3788 "potassium voltage-gated channel, delayed-rectifier, subfamily S, member 2" ion channel
KCNS3 3790 "potassium voltage-gated channel, delayed-rectifier, subfamily S, member 3" ion channel interneuron
KCNT1 57582 "potassium channel, subfamily T, member 1" ion channel
KCNT2 343450 "potassium channel, subfamily T, member 2" ion channel
KCNV1 27012 "potassium channel, subfamily V, member 1" ion channel epilepsy
KCNV2 169522 "potassium channel, subfamily V, member 2" ion channel
KCTD12 115207 potassium channel tetramerisation domain containing 12 signal transduction interneuron
KCTD4 386618 potassium channel tetramerisation domain containing 4 signal transduction
KIAA1024 23251 KIAA1024 protein other membrane protein
KIAA1199 57214 KIAA1199 other intracellular interneuron
KIAA1279 26128 KIAA1279 cytoskeletal protein microcephaly
KIAA1370 56204 KIAA1370 other intracellular
KIT 3815 v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog kinase interneuron
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
KLK6 5653 kallikrein-related peptidase 6 metabolic enzyme Alzheimer’s
KRT80 144501 keratin 80 cytoskeletal protein
KRT9 3857 keratin 9 (epidermolytic palmoplantar keratoderma) cytoskeletal protein
L1CAM 3897 L1 cell adhesion molecule cell adhesion mental retardation
LARGE 9215 like-glycosyltransferase metabolic enzyme mental retardation Hapmap
LAYN 143903 layilin other membrane protein
LDLR 3949 low density lipoprotein receptor (familial hypercholesterolemia) other membrane protein
LEPR 3953 leptin receptor other membrane protein obesity
LGALS1 3956 "lectin, galactoside-binding, soluble, 1 (galectin 1)" extracellular matrix layer 3/5
LGI1 9211 "leucine-rich, glioma inactivated 1" secreted protein epilepsy
LGI2 55203 "leucine-rich repeat LGI family, member 2" secreted protein interneuron
LGI3 203190 "leucine-rich repeat LGI family, member 3" secreted protein epilepsy
LGR4 55366 leucine-rich repeat-containing G protein-coupled receptor 4 GPCR
LGR5 8549 leucine-rich repeat-containing G protein-coupled receptor 5 GPCR
LGR6 59352 leucine-rich repeat-containing G protein-coupled receptor 6 GPCR
LHX1 3975 LIM homeobox 1 transcription factor protein evolution
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
LHX6 26468 LIM homeobox 6 transcription factor interneuron
LIG4 3981 "ligase IV, DNA, ATP-dependent" other nuclear protein microcephaly
LOC645166 645166 Similar to lymphocyte-specific protein 1 isoform 1 "HLS: (IMAGE
clone ID) 1592675"
LOC727820 727820 Hypothetical protein LOC727820 "HLS: (IMAGE
clone ID) 109123"
LOC727983 727983 Similar to Nuclear envelope pore membrane protein POM 121 (Pore membrane protein of 121 kDa) "HLS: (IMAGE
clone ID) 234376"
LOC728377 728377 Similar to rho guanine nucleotide exchange factor 5 other intracellular "HLS: (IMAGE
clone ID) 451095"
LRP1 4035 low density lipoprotein-related protein 1 (alpha-2-macroglobulin receptor) other membrane protein Alzheimer’s
LRP2 4036 low density lipoprotein-related protein 2 other membrane protein
LRP8 7804 "low density lipoprotein receptor-related protein 8, apolipoprotein e receptor" other membrane protein autism
LRRC1 55227 leucine rich repeat containing 1 signal transduction
LRRC15 131578 leucine rich repeat containing 15 cell adhesion Alzheimer’s
LRRK2 120892 leucine-rich repeat kinase 2 kinase Parkinson’s
LRRN3 54674 "leucine rich repeat protein 3, neuronal" cell adhesion autism
LSAMP 4045 limbic system-associated membrane protein cell adhesion
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
LXN 56925 latexin other intracellular
LYNX1 66004 Ly6/neurotoxin 1 secreted protein protein evolution
LYPD1 116372 LY6/PLAUR domain containing 1 secreted protein interneuron
LYPD6 130574 LY6/PLAUR domain containing 6 secreted protein
MAD1L1 8379 MAD1 mitotic arrest deficient-like 1 (yeast) other nuclear protein human accelerated regions
MAFB 9935 v-maf musculoaponeurotic fibrosarcoma oncogene homolog B (avian) transcription factor interneuron
MAOA 4128 monoamine oxidase A metabolic enzyme depression
MAOB 4129 monoamine oxidase B metabolic enzyme other neurodegenerative Hapmap
MAP1A 4130 microtubule-associated protein 1A cytoskeletal protein schizophrenia
MAPK1 5594 mitogen-activated protein kinase 1 kinase other neurodegenerative
MAPK10 5602 mitogen-activated protein kinase 10 kinase epilepsy
MAPT 4137 microtubule-associated protein tau cytoskeletal protein Alzheimer’s
MARCKSL1 65108 MARCKS-like 1 signal transduction
MBP 4155 myelin basic protein other intracellular other neurodegenerative oligodendrocyte
MC1R 4157 melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor) GPCR
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
MC2R 4158 melanocortin 2 receptor (adrenocorticotropic hormone) GPCR
MC3R 4159 melanocortin 3 receptor GPCR obesity
MC5R 4161 melanocortin 5 receptor GPCR
MCHR1 2847 melanin-concentrating hormone receptor 1 GPCR
MCHR2 84539 melanin-concentrating hormone receptor 2 GPCR
MCM7 4176 minichromosome maintenance deficient 7 (S. cerevisiae) other nuclear protein positive selection
MCPH1 79648 "microcephaly, primary autosomal recessive 1" other intracellular microcephaly protein evolution; microcephaly
MECP2 4204 methyl CpG binding protein 2 (Rett syndrome) other nuclear protein mental retardation
MEPCE 56257 methylphosphate capping enzyme metabolic enzyme positive selection
MET 4233 met proto-oncogene (hepatocyte growth factor receptor) kinase autism
MFGE8 4240 milk fat globule-EGF factor 8 protein cell adhesion layer 3
MME 4311 "membrane metallo-endopeptidase (neutral endopeptidase, enkephalinase)" other membrane protein
MOBP 4336 myelin-associated oligodendrocyte basic protein other intracellular oligodendrocyte
MOG 4340 myelin oligodendrocyte glycoprotein other membrane protein microarray expression oligodendrocyte
MPDZ 8777 multiple PDZ domain protein synaptic protein
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
MTDH 92140 metadherin other nuclear protein positive selection
MYBPC1 4604 "myosin binding protein C, slow type" cytoskeletal protein interneuron
MYL4 4635 "myosin, light polypeptide 4, alkali; atrial, embryonic" cytoskeletal protein
NAIP 4671 "NLR family, apoptosis inhibitory protein" other intracellular "HLS: (IMAGE
clone ID)755093"
NBN 4683 nibrin other nuclear protein microcephaly
NBPF14 25832 "neuroblastoma breakpoint family, member 14" other intracellular "HLS: (IMAGE
clone ID)843276"
NBPF3 84224 "neuroblastoma breakpoint family, member 3" other intracellular "HLS
amplification"
NCAM1 4684 neural cell adhesion molecule 1 cell adhesion
NDE1 54820 nudE nuclear distribution gene E homolog 1 (A. nidulans) cytoskeletal protein schizophrenia
NDEL1 81565 nudE nuclear distribution gene E homolog like 1 (A. nidulans) cytoskeletal protein schizophrenia
NEFH 4744 "neurofilament, heavy polypeptide 200kDa" cytoskeletal protein other neurodegenerative layer 5
NEFL 4747 "neurofilament, light polypeptide 68kDa" cytoskeletal protein other neurodegenerative
NEFM 4741 "neurofilament, medium polypeptide 150kDa" cytoskeletal protein
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
NEK2 4751 NIMA (never in mitosis gene a)-related kinase 2 kinase "HLS: (IMAGE
clone ID) 415089 and
2301826"
NETO2 81831 neuropilin (NRP) and tolloid (TLL)-like 2 other membrane protein
NGFB 4803 "nerve growth factor, beta polypeptide" peptide ligand other neurodegenerative
NGFR 4804 "nerve growth factor receptor (TNFR superfamily, member 16)" other membrane protein other neurodegenerative
NHEJ1 79840 nonhomologous end-joining factor 1 other nuclear protein microcephaly
NLGN1 22871 neuroligin 1 synaptic protein
NLGN2 57555 neuroligin 2 synaptic protein
NLGN3 54413 neuroligin 3 synaptic protein autism
NLGN4X 57502 neuroligin 4 synaptic protein autism
NMB 4828 neuromedin B peptide ligand
NNAT 4826 neuronatin other intracellular
NOS1 4842 nitric oxide synthase 1 (neuronal) metabolic enzyme epilepsy interneuron
NOV 4856 nephroblastoma overexpressed gene secreted protein
NPAS1 4861 neuronal PAS domain protein 1 transcription factor interneuron
NPAS3 64067 neuronal PAS domain protein 3 transcription factor schizophrenia interneuron
NPBWR2 2832 neuropeptides B/W receptor 2 GPCR
NPIPL3 23117 nuclear pore complex interacting protein-like 3 other membrane protein
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
NPR3 4883 natriuretic peptide receptor C/guanylate cyclase C (atrionatriuretic peptide receptor C) other membrane protein
NPSR1 387129 neuropeptide S receptor 1 GPCR
NPVF 64111 neuropeptide VF precursor peptide ligand
NPY 4852 neuropeptide Y peptide ligand other neurodegenerative microarray expression interneuron
NPY1R 4886 neuropeptide Y receptor Y1 GPCR autism
NPY2R 4887 neuropeptide Y receptor Y2 GPCR layer 6
NPY5R 4889 neuropeptide Y receptor Y5 GPCR epilepsy
NR2F2 7026 "nuclear receptor subfamily 2, group F, member 2" transcription factor
NR3C1 2908 "nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)" transcription factor
NR4A2 4929 "nuclear receptor subfamily 4, group A, member 2" transcription factor Parkinson’s layer 6b
NRCAM 4897 neuron-glia-CAM-related cell adhesion molecule cell adhesion autism protein evolution
NRG1 3084 neuregulin 1 other membrane protein schizophrenia
NRIP3 56675 nuclear receptor interacting protein 3 other intracellular interneuron
NRXN1 9378 neurexin I synaptic protein autism
NTF3 4908 neurotrophin 3 peptide ligand
NTNG2 84628 netrin G2 extracellular matrix layer 6
NTRK2 4915 "neurotrophic tyrosine kinase, receptor, type 2" kinase epilepsy
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
NTRK3 4916 "neurotrophic tyrosine kinase, receptor, type 3" kinase protein evolution
NTS 4922 neurotensin peptide ligand
NTSR2 23620 neurotensin receptor 2 GPCR
NUDT4 11163 Nudix (nucleoside diphosphate linked moiety X)-type motif 4 signal transduction "HLS: (IMAGE
clone ID) 768643"
NXPH1 30010 neurexophilin 1 secreted protein interneuron
OMG 4974 oligodendrocyte myelin glycoprotein cell adhesion autism
OPHN1 4983 oligophrenin 1 synaptic protein mental retardation
OPRD1 4985 "opioid receptor, delta 1" GPCR
OPRK1 4986 "opioid receptor, kappa 1" GPCR pain layer 6
OPRL1 4987 opiate receptor-like 1 GPCR
OPRM1 4988 "opioid receptor, mu 1" GPCR epilepsy protein evolution
OXT 5020 "oxytocin, prepro- (neurophysin I)" peptide ligand
OXTR 5021 oxytocin receptor GPCR autism
PAFAH1B1 5048 "platelet-activating factor acetylhydrolase, isoform Ib, alpha subunit 45kDa" metabolic enzyme schizophrenia protein evolution
PAIP1 10605 Poly(A) binding protein interacting protein 1 signal transduction "HLS: (IMAGE
clone ID) 231802"
PAK2 5062 P21 (CDKN1A)-activated kinase 2 kinase epilepsy "HLS: (IMAGE
clone ID) 136324"
PAK3 5063 p21 (CDKN1A)-activated kinase 3 kinase mental retardation
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
PARK2 5071 "Parkinson’s disease (autosomal recessive, juvenile) 2, parkin" other intracellular Parkinson’s
PARK7 11315 "Parkinson’s disease (autosomal recessive, early onset) 7" other intracellular Parkinson’s
PARM1 25849 prostate androgen-regulated mucin- like protein 1 other membrane protein
PAX6 5080 "paired box gene 6 (aniridia, keratitis)" transcription factor microcephaly
PCDH17 27253 protocadherin 17 cell adhesion frontal cortex expression layer 6
PCDH18 54510 protocadherin 18 cell adhesion interneuron
PCDH20 64881 protocadherin 20 cell adhesion layer 5/6
PCDHA6 56142 protocadherin alpha 6 cell adhesion
PCNT 5116 pericentrin (kendrin) cytoskeletal protein schizophrenia
PCP4 5121 Purkinje cell protein 4 other intracellular layer 5/6
PDE10A 10846 phosphodiesterase 10A signal transduction
PDE1A 5136 "phosphodiesterase 1A, calmodulin- dependent" signal transduction depression layer 5/6
PDE4B 5142 "phosphodiesterase 4B, cAMP-specific (phosphodiesterase E4 dunce homolog, Drosophila)" signal transduction schizophrenia
PDE4DIP 9659 phosphodiesterase 4D interacting protein (myomegalin) signal transduction microarray expression; HLS (IMAGE clone ID) 2170455
PDE5A 8654 "phosphodiesterase 5A, cGMP-specific" signal transduction
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
PDHX 8050 "pyruvate dehydrogenase complex, component X" metabolic enzyme mental retardation
PDLIM5 10611 PDZ and LIM domain 5 cytoskeletal protein schizophrenia
PDYN 5173 prodynorphin peptide ligand epilepsy promoter interneuron/ layer4
PEG3 5178 paternally expressed 3 transcription factor protein evolution
PENK 5179 proenkephalin 1 peptide ligand layer 2/3/6
PHF8 23133 PHD finger protein 8 other nuclear protein mental retardation
PHGDH 26227 phosphoglycerate dehydrogenase metabolic enzyme microcephaly
PIK3CB 5291 "phosphoinositide-3-kinase, catalytic, beta polypeptide" kinase
PIK3CG 5294 "phosphoinositide-3-kinase, catalytic, gamma polypeptide" kinase autism
PINK1 65018 PTEN induced putative kinase 1 kinase Parkinson’s
PLAU 5328 "plasminogen activator, urokinase" extracellular matrix Alzheimer’s
PLAUR 5329 urokinase plasminogen activator receptor extracellular matrix autism
PLTP 5360 phospholipid transfer protein secreted protein VEC
PLXNA2 5362 plexin A2 kinase schizophrenia
PLXND1 23129 plexin D1 kinase
PMCH 5367 pro-melanin-concentrating hormone peptide ligand
PNOC 5368 prepronociceptin peptide ligand interneuron
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
POM121 9883 POM121 membrane glycoprotein (rat) other nuclear protein "HLS: (IMAGE
clone ID) 548957"
POMT1 10585 protein-O-mannosyltransferase 1 metabolic enzyme microcephaly
PPAP2B 8613 phosphatidic acid phosphatase type 2B signal transduction astrocyte
PPP1R1B 84152 "protein phosphatase 1, regulatory (inhibitor) subunit 1B (dopamine and cAMP regulated phosphoprotein, DARPP-32)" signal transduction schizophrenia
PPP3CA 5530 "protein phosphatase 3 (formerly 2B), catalytic subunit, alpha isoform (calcineurin A alpha)" signal transduction schizophrenia
PPP3CB 5532 "protein phosphatase 3 (formerly 2B), catalytic subunit, beta isoform" signal transduction
PPP3CC 5533 "protein phosphatase 3 (formerly 2B), catalytic subunit, gamma isoform" signal transduction schizophrenia
PQBP1 10084 polyglutamine binding protein 1 other nuclear protein mental retardation
PRKCB 5579 "protein kinase C, beta" kinase autism
PRKCG 5582 "protein kinase C, gamma" kinase other neurodegenerative
PRLH 51052 prolactin releasing hormone peptide ligand
PRLHR 2834 prolactin releasing hormone receptor GPCR
PRODH 5625 proline dehydrogenase (oxidase) 1 metabolic enzyme schizophrenia CNV interneuron
PRSS12 8492 "protease, serine, 12 (neurotrypsin, motopsin)" secreted protein mental retardation CNV layer 5/6
PRSS23 11098 "protease, serine, 23" secreted protein
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
PSEN1 5663 presenilin 1 (Alzheimer’s disease 3) other membrane protein Alzheimer’s
PSEN2 5664 presenilin 2 (Alzheimer’s disease 4) other membrane protein Alzheimer’s
PTEN 5728 phosphatase and tensin homolog signal transduction autism
PTGS2 5743 prostaglandin-endoperoxide synthase 2 (Ptgs2) metabolic enzyme autism
PTHLH 5744 parathyroid hormone-like hormone peptide ligand interneuron
PVALB 5816 Parvalbumin signal transduction schizophrenia interneuron
PVRL3 25945 poliovirus receptor-related 3 cell adhesion layer 2/3
QDPR 5860 quinoid dihydropteridine reductase metabolic enzyme microcephaly oligodendrocyte
QRFPR 84109 pyroglutamylated RFamide peptide receptor GPCR
RAB3B 5865 "RAB3B, member RAS oncogene family" signal transduction
RAB3C 115827 "RAB3C, member RAS oncogene family" signal transduction interneuron
RAB3GAP1 22930 RAB3 GTPase activating protein subunit 1 (catalytic) signal transduction mental retardation
RAB3IP 117177 RAB3A interacting protein (rabin3) signal transduction positive selection
RAB6A 5870 "RAB6A, member RAS oncogene family" signal transduction "HLS: (IMAGE
clone ID) 321470"
RANBP9 10048 RAN binding protein 9 signal transduction schizophrenia
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
RAPGEF4 11069 Rap guanine nucleotide exchange factor (GEF) 4 signal transduction autism
RASGRF2 5924 Ras protein-specific guanine nucleotide-releasing factor 2 signal transduction layer 2/3
RASSF7 8045 Ras association (RalGDS/AF-6) domain family 7 signal transduction schizophrenia
RELN 5649 reelin extracellular matrix autism interneuron
REST 5978 RE1-silencing transcription factor (Rest) transcription factor
RGS10 6001 regulator of G-protein signalling 10 signal transduction
RGS4 5999 regulator of G-protein signalling 4 signal transduction schizophrenia
RNASEH2A 10535 "ribonuclease H2, subunit A" other nuclear protein microcephaly
RNASEH2B 79621 "ribonuclease H2, subunit B" other nuclear protein microcephaly
RNASEH2C 84153 "ribonuclease H2, subunit C" other nuclear protein microcephaly
RND2 8153 Rho family GTPase 2 signal transduction
RNF144B 255488 ring finger protein 144B other membrane protein interneuron
ROCK1 6093 "Rho-associated, coiled-coil containing protein kinase 1" kinase "HLS: (IMAGE
clone ID) 824758"
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
RORB 6096 RAR-related orphan receptor B transcription factor microarray expression layer 4
RPRM 56475 "reprimo, TP53 dependent G2 arrest mediator candidate" signal transduction layer 5/6
RPS6KA3 6197 "ribosomal protein S6 kinase, 90kDa, polypeptide 3" kinase mental retardation
RRP8 23378 "ribosomal RNA processing 8, methyltransferase, homolog (yeast)" other nuclear protein positive selection
RSPO1 284654 R-spondin homolog (Xenopus laevis) secreted protein
RTN4 57142 reticulon 4 other membrane protein schizophrenia
RTN4R 65078 reticulon 4 receptor other membrane protein schizophrenia
RXFP1 59350 relaxin/insulin-like family peptide receptor 1 GPCR layer 5/6
RXFP3 51289 relaxin/insulin-like family peptide receptor 3 GPCR
RXFP4 339403 relaxin/insulin-like family peptide receptor 4 GPCR
S100A10 6281 S100 calcium binding protein A10 signal transduction
S100B 6285 S100 calcium binding protein B signal transduction other neurodegenerative oligodendrocyte
SCN10A 6336 "sodium channel, voltage-gated, type X, alpha" ion channel
SCN11A 11280 "sodium channel, voltage-gated, type XI, alpha" ion channel
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
SCN1A 6323 "sodium channel, voltage-gated, type I, alpha" ion channel epilepsy
SCN1B 6324 "sodium channel, voltage-gated, type I, beta" ion channel epilepsy
SCN2A 6326 "sodium channel, voltage-gated, type II, alpha subunit" ion channel epilepsy
SCN2B 6327 "sodium channel, voltage-gated, type II, beta" ion channel epilepsy
SCN3A 6328 "sodium channel, voltage-gated, type III, alpha" ion channel
SCN3B 55800 "sodium channel, voltage-gated, type III, beta" ion channel layer 2/3/6
SCN4A 6329 "sodium channel, voltage-gated, type IV, alpha" ion channel
SCN4B 6330 "sodium channel, voltage-gated, type IV, beta" ion channel layer 3/5
SCN5A 6331 "sodium channel, voltage-gated, type V, alpha (long QT syndrome 3)" ion channel epilepsy
SCN7A 6332 "sodium channel, voltage-gated, type VII, alpha" ion channel
SCN8A 6334 "sodium channel, voltage gated, type VIII, alpha" ion channel
SCN9A 6335 "sodium channel, voltage-gated, type IX, alpha" ion channel
SCNN1A 6337 "sodium channel, nonvoltage-gated 1 alpha" ion channel
SCNN1B 6338 "sodium channel, nonvoltage-gated 1, beta (Liddle syndrome)" ion channel
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category
Gene Symbol EntrezID Gene Description Gene Family Disease Comparative Genomics Marker Type
SCNN1D 6339 "sodium channel, nonvoltage-gated 1, delta" ion channel
SCNN1G 6340 "sodium channel, nonvoltage-gated 1, gamma" ion channel
SCRT1 83482 "scratch homolog 1, zinc finger protein (Drosophila)" transcription factor
SDK1 221935 sidekick homolog 1 (chicken) cell adhesion CNV
SEMA3C 10512 "sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C" secreted protein interneuron/ layer6
SEMA3F 6405 "sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F" secreted protein
SEMA4G 57715 "sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4G" secreted protein
SEMA5B 54437 "sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B" secreted protein
SERF1A 8293 Small EDRK-rich factor 1A (telomeric) other intracellular "HLS: (IMAGE
clone ID) 767345 and
305677 and
191877"
SGK 6446 serum/glucocorticoid regulated kinase kinase other neurodegenerative
"Table 1. Genes characterized by ISH in 1,000 gene survey in cortex (Cortex Study)."
Category