sensory perception of light stimulus Gene Set

Dataset GO Biological Process Annotations
Category structural or functional annotations
Type biological process
Description The series of events required for an organism to receive a sensory light stimulus, convert it to a molecular signal, and recognize and characterize the signal. This is a neurological process. (Gene Ontology, GO_0050953)
External Link http://amigo.geneontology.org/amigo/term/GO:0050953
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Genes

189 genes participating in the sensory perception of light stimulus biological process from the curated GO Biological Process Annotations dataset.

Symbol Name
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4
ABCC6 ATP-binding cassette, sub-family C (CFTR/MRP), member 6
ABLIM1 actin binding LIM protein 1
ADGRV1 adhesion G protein-coupled receptor V1
AIPL1 aryl hydrocarbon receptor interacting protein-like 1
AOC2 amine oxidase, copper containing 2 (retina-specific)
ARL6 ADP-ribosylation factor-like 6
ARR3 arrestin 3, retinal (X-arrestin)
ATXN7 ataxin 7
BBS1 Bardet-Biedl syndrome 1
BBS10 Bardet-Biedl syndrome 10
BBS2 Bardet-Biedl syndrome 2
BBS4 Bardet-Biedl syndrome 4
BBS5 Bardet-Biedl syndrome 5
BBS7 Bardet-Biedl syndrome 7
BBS9 Bardet-Biedl syndrome 9
BEST1 bestrophin 1
BFSP2 beaded filament structural protein 2, phakinin
C2ORF71 chromosome 2 open reading frame 71
CABP4 calcium binding protein 4
CACNA1F calcium channel, voltage-dependent, L type, alpha 1F subunit
CACNB2 calcium channel, voltage-dependent, beta 2 subunit
CDH23 cadherin-related 23
CDH3 cadherin 3, type 1, P-cadherin (placental)
CHM choroideremia (Rab escort protein 1)
CHRNB2 cholinergic receptor, nicotinic, beta 2 (neuronal)
CLDN19 claudin 19
CLN6 ceroid-lipofuscinosis, neuronal 6, late infantile, variant
CLN8 ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)
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
COL11A1 collagen, type XI, alpha 1
COL18A1 collagen, type XVIII, alpha 1
COL1A1 collagen, type I, alpha 1
COL2A1 collagen, type II, alpha 1
CRX cone-rod homeobox
CRYBA1 crystallin, beta A1
CRYBA4 crystallin, beta A4
CRYBB1 crystallin, beta B1
CRYBB2 crystallin, beta B2
CRYBB3 crystallin, beta B3
CRYGA crystallin, gamma A
CRYGB crystallin, gamma B
CRYGC crystallin, gamma C
CRYGD crystallin, gamma D
CRYZ crystallin, zeta (quinone reductase)
CYP1B1 cytochrome P450, family 1, subfamily B, polypeptide 1
CYP4V2 cytochrome P450, family 4, subfamily V, polypeptide 2
DFNB31 deafness, autosomal recessive 31
DHRS3 dehydrogenase/reductase (SDR family) member 3
DLL4 delta-like 4 (Drosophila)
DNAJC19 DnaJ (Hsp40) homolog, subfamily C, member 19
EFEMP1 EGF containing fibulin-like extracellular matrix protein 1
EML2 echinoderm microtubule associated protein like 2
EPAS1 endothelial PAS domain protein 1
EYA3 EYA transcriptional coactivator and phosphatase 3
EYA4 EYA transcriptional coactivator and phosphatase 4
FAM161A family with sequence similarity 161, member A
FSCN2 fascin actin-bundling protein 2, retinal
GABRR2 gamma-aminobutyric acid (GABA) A receptor, rho 2
GJA3 gap junction protein, alpha 3, 46kDa
GJA8 gap junction protein, alpha 8, 50kDa
GJC1 gap junction protein, gamma 1, 45kDa
GJD2 gap junction protein, delta 2, 36kDa
GLRA1 glycine receptor, alpha 1
GLRB glycine receptor, beta
GNAT1 guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 1
GNAT2 guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2
GPR143 G protein-coupled receptor 143
GPR179 G protein-coupled receptor 179
GRK1 G protein-coupled receptor kinase 1
GRK7 G protein-coupled receptor kinase 7
GRM8 glutamate receptor, metabotropic 8
GUCA1A guanylate cyclase activator 1A (retina)
GUCA1B guanylate cyclase activator 1B (retina)
GUCA1C guanylate cyclase activator 1C
GUCY2D guanylate cyclase 2D, membrane (retina-specific)
GUCY2F guanylate cyclase 2F, retinal
HMCN1 hemicentin 1
HPS1 Hermansky-Pudlak syndrome 1
IMPG1 interphotoreceptor matrix proteoglycan 1
IMPG2 interphotoreceptor matrix proteoglycan 2
IRX5 iroquois homeobox 5
KCNJ10 potassium channel, inwardly rectifying subfamily J, member 10
KERA keratocan
KIFC3 kinesin family member C3
KRT12 keratin 12, type I
LAMB2 laminin, beta 2 (laminin S)
LAMC3 laminin, gamma 3
LRAT lecithin retinol acyltransferase (phosphatidylcholine--retinol O-acyltransferase)
LUM lumican
MIP major intrinsic protein of lens fiber
MKKS McKusick-Kaufman syndrome
MYO3A myosin IIIA
MYO3B myosin IIIB
MYO5A myosin VA (heavy chain 12, myoxin)
MYO7A myosin VIIA
MYO9A myosin IXA
NDP Norrie disease (pseudoglioma)
NOB1 NIN1/RPN12 binding protein 1 homolog (S. cerevisiae)
NR2E1 nuclear receptor subfamily 2, group E, member 1
NR2E3 nuclear receptor subfamily 2, group E, member 3
NRL neural retina leucine zipper
NXNL2 nucleoredoxin-like 2
NYX nyctalopin
OAT ornithine aminotransferase
OCLM oculomedin
OPA1 optic atrophy 1 (autosomal dominant)
OPA3 optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
OPN1SW opsin 1 (cone pigments), short-wave-sensitive
OPN4 opsin 4
OPN5 opsin 5
PAX2 paired box 2
PAX6 paired box 6
PCDH15 protocadherin-related 15
PDC phosducin
PDCL phosducin-like
PDE6A phosphodiesterase 6A, cGMP-specific, rod, alpha
PDE6B phosphodiesterase 6B, cGMP-specific, rod, beta
PDE6C phosphodiesterase 6C, cGMP-specific, cone, alpha prime
PDE6D phosphodiesterase 6D, cGMP-specific, rod, delta
PDE6G phosphodiesterase 6G, cGMP-specific, rod, gamma
PDE6H phosphodiesterase 6H, cGMP-specific, cone, gamma
PITPNA phosphatidylinositol transfer protein, alpha
POU4F3 POU class 4 homeobox 3
POU6F2 POU class 6 homeobox 2
PPEF2 protein phosphatase, EF-hand calcium binding domain 2
PPT1 palmitoyl-protein thioesterase 1
PRCD progressive rod-cone degeneration
PRPH2 peripherin 2 (retinal degeneration, slow)
PRR4 proline rich 4 (lacrimal)
RABGGTA Rab geranylgeranyltransferase, alpha subunit
RABGGTB Rab geranylgeranyltransferase, beta subunit
RAX retina and anterior neural fold homeobox
RAX2 retina and anterior neural fold homeobox 2
RBP3 retinol binding protein 3, interstitial
RCVRN recoverin
RD3 retinal degeneration 3
RDH10 retinol dehydrogenase 10 (all-trans)
RDH12 retinol dehydrogenase 12 (all-trans/9-cis/11-cis)
RDH5 retinol dehydrogenase 5 (11-cis/9-cis)
RDH8 retinol dehydrogenase 8 (all-trans)
RGR retinal G protein coupled receptor
RGS16 regulator of G-protein signaling 16
RGS9 regulator of G-protein signaling 9
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)
RPE65 retinal pigment epithelium-specific protein 65kDa
RPGR retinitis pigmentosa GTPase regulator
RPGRIP1 retinitis pigmentosa GTPase regulator interacting protein 1
RRH retinal pigment epithelium-derived rhodopsin homolog
RS1 retinoschisin 1
SAG S-antigen; retina and pineal gland (arrestin)
SFRP5 secreted frizzled-related protein 5
SIX3 SIX homeobox 3
SIX6 SIX homeobox 6
SLC24A1 solute carrier family 24 (sodium/potassium/calcium exchanger), member 1
SLC24A2 solute carrier family 24 (sodium/potassium/calcium exchanger), member 2
SLC45A2 solute carrier family 45, member 2
SLITRK6 SLIT and NTRK-like family, member 6
SOX14 SRY (sex determining region Y)-box 14
SPATA7 spermatogenesis associated 7
TACSTD2 tumor-associated calcium signal transducer 2
TGFBI transforming growth factor, beta-induced, 68kDa
TH tyrosine hydroxylase
TIMP3 TIMP metallopeptidase inhibitor 3
TRPM1 transient receptor potential cation channel, subfamily M, member 1
TULP1 tubby like protein 1
TULP2 tubby like protein 2
TYR tyrosinase
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)
VAX2 ventral anterior homeobox 2
VSX1 visual system homeobox 1
VSX2 visual system homeobox 2
WDR36 WD repeat domain 36
WFS1 Wolfram syndrome 1 (wolframin)
ZIC2 Zic family member 2
ZNF513 zinc finger protein 513