sensory system disease Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A nervous system disease which is located in a part of the nervous system responsible for processing sensory information that consists of sensory receptors, neural pathways, and parts of the brain involved in sensory perception. Commonly recognized sensory systems are those for vision, hearing, somatic sensation (touch), taste and olfaction (smell). (Human Disease Ontology, DOID_0050155)
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Genes

300 genes involed in the disease sensory system disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4
ABCB6 ATP-binding cassette, sub-family B (MDR/TAP), member 6 (Langereis blood group)
ABHD12 abhydrolase domain containing 12
ABHD5 abhydrolase domain containing 5
ACTG1 actin gamma 1
ADAM9 ADAM metallopeptidase domain 9
ADCY1 adenylate cyclase 1 (brain)
ADGRV1 adhesion G protein-coupled receptor V1
AGK acylglycerol kinase
AGPS alkylglycerone phosphate synthase
AIPL1 aryl hydrocarbon receptor interacting protein-like 1
ALDH1A3 aldehyde dehydrogenase 1 family, member A3
ALMS1 Alstrom syndrome protein 1
APOE apolipoprotein E
ARL6 ADP-ribosylation factor-like 6
ASB10 ankyrin repeat and SOCS box containing 10
ASPM asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
BCOR BCL6 corepressor
BEST1 bestrophin 1
BFSP1 beaded filament structural protein 1, filensin
BFSP2 beaded filament structural protein 2, phakinin
BMP4 bone morphogenetic protein 4
C1QTNF5 C1q and tumor necrosis factor related protein 5
C2 complement component 2
C2ORF71 chromosome 2 open reading frame 71
C3 complement component 3
C8ORF37 chromosome 8 open reading frame 37
C9 complement component 9
CA4 carbonic anhydrase IV
CABP2 calcium binding protein 2
CABP4 calcium binding protein 4
CACNA1F calcium channel, voltage-dependent, L type, alpha 1F subunit
CCDC50 coiled-coil domain containing 50
CDH23 cadherin-related 23
CDHR1 cadherin-related family member 1
CEACAM16 carcinoembryonic antigen-related cell adhesion molecule 16
CEP290 centrosomal protein 290kDa
CERKL ceramide kinase-like
CETP cholesteryl ester transfer protein, plasma
CFB complement factor B
CFH complement factor H
CFHR2 complement factor H-related 2
CFHR4 complement factor H-related 4
CFHR5 complement factor H-related 5
CFI complement factor I
CHM choroideremia (Rab escort protein 1)
CHMP4B charged multivesicular body protein 4B
CHN1 chimerin 1
CIB2 calcium and integrin binding family member 2
CLDN14 claudin 14
CLRN1 clarin 1
CNGA1 cyclic nucleotide gated channel alpha 1
CNGA3 cyclic nucleotide gated channel alpha 3
CNGB1 cyclic nucleotide gated channel beta 1
CNGB3 cyclic nucleotide gated channel beta 3
CNNM4 cyclin and CBS domain divalent metal cation transport mediator 4
COCH cochlin
COL11A1 collagen, type XI, alpha 1
COL11A2 collagen, type XI, alpha 2
COL11A2P1 collagen, type XI, alpha 2 pseudogene 1
COL2A1 collagen, type II, alpha 1
COL4A6 collagen, type IV, alpha 6
CRB1 crumbs family member 1, photoreceptor morphogenesis associated
CRX cone-rod homeobox
CRYAA crystallin, alpha A
CRYAB crystallin, alpha B
CRYBA1 crystallin, beta A1
CRYBA2 crystallin, beta A2
CRYBA4 crystallin, beta A4
CRYBB1 crystallin, beta B1
CRYBB2 crystallin, beta B2
CRYBB3 crystallin, beta B3
CRYGB crystallin, gamma B
CRYGC crystallin, gamma C
CRYGD crystallin, gamma D
CRYGS crystallin, gamma S
CST3 cystatin C
CTDP1 CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1
CX3CR1 chemokine (C-X3-C motif) receptor 1
CYP1B1 cytochrome P450, family 1, subfamily B, polypeptide 1
CYP27A1 cytochrome P450, family 27, subfamily A, polypeptide 1
DFNA5 deafness, autosomal dominant 5
DFNB31 deafness, autosomal recessive 31
DFNB59 deafness, autosomal recessive 59
DHDDS dehydrodolichyl diphosphate synthase
DIABLO diablo, IAP-binding mitochondrial protein
DIAPH1 diaphanous-related formin 1
DIAPH3 diaphanous-related formin 3
DMPK dystrophia myotonica-protein kinase
EBP emopamil binding protein (sterol isomerase)
ELMOD3 ELMO/CED-12 domain containing 3
ELOVL4 ELOVL fatty acid elongase 4
EPG5 ectopic P-granules autophagy protein 5 homolog (C. elegans)
EPHA2 EPH receptor A2
ERCC1 excision repair cross-complementation group 1
ERCC2 excision repair cross-complementation group 2
ERCC6 excision repair cross-complementation group 6
ESPN espin
ESRRB estrogen-related receptor beta
EYA4 EYA transcriptional coactivator and phosphatase 4
EYS eyes shut homolog (Drosophila)
F13B coagulation factor XIII, B polypeptide
FAM126A family with sequence similarity 126, member A
FAM161A family with sequence similarity 161, member A
FBLN5 fibulin 5
FLVCR1 feline leukemia virus subgroup C cellular receptor 1
FOXC1 forkhead box C1
FOXE3 forkhead box E3
FSCN2 fascin actin-bundling protein 2, retinal
FTL ferritin, light polypeptide
FYCO1 FYVE and coiled-coil domain containing 1
FZD4 frizzled class receptor 4
GALK1 galactokinase 1
GALT galactose-1-phosphate uridylyltransferase
GDF3 growth differentiation factor 3
GDF6 growth differentiation factor 6
GFER growth factor, augmenter of liver regeneration
GJA1 gap junction protein, alpha 1, 43kDa
GJA3 gap junction protein, alpha 3, 46kDa
GJA8 gap junction protein, alpha 8, 50kDa
GJB2 gap junction protein, beta 2, 26kDa
GJB3 gap junction protein, beta 3, 31kDa
GJB6 gap junction protein, beta 6, 30kDa
GNAT1 guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 1
GNPAT glyceronephosphate O-acyltransferase
GPR143 G protein-coupled receptor 143
GPR179 G protein-coupled receptor 179
GRHL2 grainyhead-like 2 (Drosophila)
GRK1 G protein-coupled receptor kinase 1
GRM6 glutamate receptor, metabotropic 6
GRXCR1 glutaredoxin, cysteine rich 1
GRXCR2 glutaredoxin, cysteine rich 2
GUCA1B guanylate cyclase activator 1B (retina)
GUCY2D guanylate cyclase 2D, membrane (retina-specific)
HARS histidyl-tRNA synthetase
HCCS holocytochrome c synthase
HGF hepatocyte growth factor (hepapoietin A; scatter factor)
HMCN1 hemicentin 1
HMGB3 high mobility group box 3
HMX1 H6 family homeobox 1
HSF4 heat shock transcription factor 4
HTRA1 HtrA serine peptidase 1
IDH3B isocitrate dehydrogenase 3 (NAD+) beta
ILDR1 immunoglobulin-like domain containing receptor 1
IMPDH1 IMP (inosine 5'-monophosphate) dehydrogenase 1
IMPG2 interphotoreceptor matrix proteoglycan 2
KARS lysyl-tRNA synthetase
KCNJ13 potassium channel, inwardly rectifying subfamily J, member 13
KCNQ4 potassium channel, voltage gated KQT-like subfamily Q, member 4
KCNV2 potassium channel, voltage gated modifier subfamily V, member 2
KLHL7 kelch-like family member 7
LCA5 Leber congenital amaurosis 5
LHFPL5 lipoma HMGIC fusion partner-like 5
LIM2 lens intrinsic membrane protein 2, 19kDa
LIPC lipase, hepatic
LOXHD1 lipoxygenase homology domains 1
LOXL1 lysyl oxidase-like 1
LRAT lecithin retinol acyltransferase (phosphatidylcholine--retinol O-acyltransferase)
LRIT3 leucine-rich repeat, immunoglobulin-like and transmembrane domains 3
LRP5 low density lipoprotein receptor-related protein 5
LTBP2 latent transforming growth factor beta binding protein 2
MAF v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog
MAK male germ cell-associated kinase
MAP2 microtubule-associated protein 2
MARVELD2 MARVEL domain containing 2
MERTK MER proto-oncogene, tyrosine kinase
MFRP membrane frizzled-related protein
MIP major intrinsic protein of lens fiber
MSRB3 methionine sulfoxide reductase B3
MVK mevalonate kinase
MYH14 myosin, heavy chain 14, non-muscle
MYH9 myosin, heavy chain 9, non-muscle
MYO15A myosin XVA
MYO1A myosin IA
MYO3A myosin IIIA
MYO6 myosin VI
MYO7A myosin VIIA
MYOC myocilin, trabecular meshwork inducible glucocorticoid response
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
NDP Norrie disease (pseudoglioma)
NEK2 NIMA-related kinase 2
NHS Nance-Horan syndrome (congenital cataracts and dental anomalies)
NMNAT1 nicotinamide nucleotide adenylyltransferase 1
NR2E3 nuclear receptor subfamily 2, group E, member 3
NRL neural retina leucine zipper
NTF4 neurotrophin 4
NYX nyctalopin
OCRL oculocerebrorenal syndrome of Lowe
OPA3 optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
OPTN optineurin
OTOA otoancorin
OTOF otoferlin
OTOG otogelin
OTOGL otogelin-like
OTX2 orthodenticle homeobox 2
P2RX2 purinergic receptor P2X, ligand gated ion channel, 2
PABPN1 poly(A) binding protein, nuclear 1
PAX6 paired box 6
PCDH15 protocadherin-related 15
PCYT1A phosphate cytidylyltransferase 1, choline, alpha
PDE6A phosphodiesterase 6A, cGMP-specific, rod, alpha
PDE6B phosphodiesterase 6B, cGMP-specific, rod, beta
PDE6G phosphodiesterase 6G, cGMP-specific, rod, gamma
PDZD7 PDZ domain containing 7
PEX7 peroxisomal biogenesis factor 7
PHYH phytanoyl-CoA 2-hydroxylase
PITPNM3 PITPNM family member 3
PITX2 paired-like homeodomain 2
PITX3 paired-like homeodomain 3
PNPT1 polyribonucleotide nucleotidyltransferase 1
POU3F4 POU class 3 homeobox 4
POU4F3 POU class 4 homeobox 3
PRCD progressive rod-cone degeneration
PROM1 prominin 1
PRPF3 pre-mRNA processing factor 3
PRPF31 pre-mRNA processing factor 31
PRPF6 pre-mRNA processing factor 6
PRPF8 pre-mRNA processing factor 8
PRPH2 peripherin 2 (retinal degeneration, slow)
PRPS1 phosphoribosyl pyrophosphate synthetase 1
PTPRQ protein tyrosine phosphatase, receptor type, Q
RAB28 RAB28, member RAS oncogene family
RAB3GAP2 RAB3 GTPase activating protein subunit 2 (non-catalytic)
RARB retinoic acid receptor, beta
RAX retina and anterior neural fold homeobox
RAX2 retina and anterior neural fold homeobox 2
RB1 retinoblastoma 1
RBP3 retinol binding protein 3, interstitial
RD3 retinal degeneration 3
RDH12 retinol dehydrogenase 12 (all-trans/9-cis/11-cis)
RDX radixin
RECQL4 RecQ protein-like 4
RGR retinal G protein coupled receptor
RHO rhodopsin
RIMS1 regulating synaptic membrane exocytosis 1
RLBP1 retinaldehyde binding protein 1
ROM1 retinal outer segment membrane protein 1
RP1 retinitis pigmentosa 1 (autosomal dominant)
RP2 retinitis pigmentosa 2 (X-linked recessive)
RP9 retinitis pigmentosa 9 (autosomal dominant)
RPE65 retinal pigment epithelium-specific protein 65kDa
RPGR retinitis pigmentosa GTPase regulator
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1
SAG S-antigen; retina and pineal gland (arrestin)
SDCCAG8 serologically defined colon cancer antigen 8
SEMA4A sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A
SERPINB6 serpin peptidase inhibitor, clade B (ovalbumin), member 6
SHH sonic hedgehog
SIX1 SIX homeobox 1
SIX6 SIX homeobox 6
SLC16A12 solute carrier family 16, member 12
SLC17A8 solute carrier family 17 (vesicular glutamate transporter), member 8
SLC24A1 solute carrier family 24 (sodium/potassium/calcium exchanger), member 1
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SLC26A5 solute carrier family 26 (anion exchanger), member 5
SLC33A1 solute carrier family 33 (acetyl-CoA transporter), member 1
SLC4A4 solute carrier family 4 (sodium bicarbonate cotransporter), member 4
SLC7A14 solute carrier family 7, member 14
SMOC1 SPARC related modular calcium binding 1
SMPX small muscle protein, X-linked
SNRNP200 small nuclear ribonucleoprotein 200kDa (U5)
SNX3 sorting nexin 3
SOX2 SRY (sex determining region Y)-box 2
SPATA7 spermatogenesis associated 7
SRD5A3 steroid 5 alpha-reductase 3
STRA6 stimulated by retinoic acid 6
STRC stereocilin
STRCP1 stereocilin pseudogene 1
SYNE4 spectrin repeat containing, nuclear envelope family member 4
TBC1D24 TBC1 domain family, member 24
TBK1 TANK-binding kinase 1
TDRD7 tudor domain containing 7
TECTA tectorin alpha
TIMP3 TIMP metallopeptidase inhibitor 3
TLR4 toll-like receptor 4
TMC1 transmembrane channel-like 1
TMIE transmembrane inner ear
TMPRSS3 transmembrane protease, serine 3
TNC tenascin C
TOPORS topoisomerase I binding, arginine/serine-rich, E3 ubiquitin protein ligase
TPRN taperin
TRIOBP TRIO and F-actin binding protein
TRPM1 transient receptor potential cation channel, subfamily M, member 1
TSPEAR thrombospondin-type laminin G domain and EAR repeats
TTC8 tetratricopeptide repeat domain 8
TTLL5 tubulin tyrosine ligase-like family member 5
TULP1 tubby like protein 1
UNC119 unc-119 homolog (C. elegans)
USH1C Usher syndrome 1C (autosomal recessive, severe)
USH1G Usher syndrome 1G (autosomal recessive)
USH2A Usher syndrome 2A (autosomal recessive, mild)
VAX1 ventral anterior homeobox 1
VCAN versican
VIM vimentin
VSX2 visual system homeobox 2
WDR19 WD repeat domain 19
WDR36 WD repeat domain 36
WFS1 Wolfram syndrome 1 (wolframin)
ZNF513 zinc finger protein 513