sensory perception of light stimulus Gene Set

Dataset GO Biological Process Annotations 2023
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
Similar Terms
Downloads & Tools

Genes

103 genes participating in the sensory perception of light stimulus biological process from the curated GO Biological Process Annotations 2023 dataset.

Symbol Name
ABLIM1 actin binding LIM protein 1
ADGRV1 adhesion G protein-coupled receptor V1
AOC2 amine oxidase, copper containing 2 (retina-specific)
ARR3 arrestin 3, retinal (X-arrestin)
ARRB1 arrestin, beta 1
ATF6 activating transcription factor 6
ATXN7 ataxin 7
BBS2 Bardet-Biedl syndrome 2
BEST1 bestrophin 1
CABP2 calcium binding protein 2
CABP4 calcium binding protein 4
CACNA1F calcium channel, voltage-dependent, L type, alpha 1F subunit
CDH23 cadherin-related 23
CHRNB2 cholinergic receptor, nicotinic, beta 2 (neuronal)
CLRN1 clarin 1
CNGB1 cyclic nucleotide gated channel beta 1
COL11A1 collagen, type XI, alpha 1
COL18A1 collagen, type XVIII, alpha 1
COL1A1 collagen, type I, alpha 1
COL2A1 collagen, type II, alpha 1
CRYAA crystallin, alpha A
CRYBA1 crystallin, beta A1
CRYBA2 crystallin, beta A2
CRYBA4 crystallin, beta A4
CRYBB1 crystallin, beta B1
CRYBB2 crystallin, beta B2
CRYBB3 crystallin, beta B3
CRYBG3 beta-gamma crystallin domain containing 3
CRYGA crystallin, gamma A
CRYGB crystallin, gamma B
CRYGC crystallin, gamma C
CRYGD crystallin, gamma D
CRYGN crystallin, gamma N
CRYGS crystallin, gamma S
CRYZ crystallin, zeta (quinone reductase)
DFNB31 deafness, autosomal recessive 31
DHRS3 dehydrogenase/reductase (SDR family) member 3
DNAJC19 DnaJ (Hsp40) homolog, subfamily C, member 19
DRAM2 DNA-damage regulated autophagy modulator 2
E2F1 E2F transcription factor 1
EFEMP1 EGF containing fibulin-like extracellular matrix protein 1
EML2 echinoderm microtubule associated protein like 2
EYA3 EYA transcriptional coactivator and phosphatase 3
EYA4 EYA transcriptional coactivator and phosphatase 4
FSCN2 fascin actin-bundling protein 2, retinal
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
GRM8 glutamate receptor, metabotropic 8
GUCA1A guanylate cyclase activator 1A (retina)
GUCA1B guanylate cyclase activator 1B (retina)
GUCA1C guanylate cyclase activator 1C
GUCY2F guanylate cyclase 2F, retinal
IMPG2 interphotoreceptor matrix proteoglycan 2
KIFC3 kinesin family member C3
KRT12 keratin 12, type I
LUM lumican
MYO7A myosin VIIA
MYO9A myosin IXA
NXNL2 nucleoredoxin-like 2
OAT ornithine aminotransferase
OPA1 optic atrophy 1 (autosomal dominant)
OPA3 optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
PAX2 paired box 2
PAX6 paired box 6
PCDH15 protocadherin-related 15
PDE6C phosphodiesterase 6C, cGMP-specific, cone, alpha prime
PITPNA phosphatidylinositol transfer protein, alpha
POU4F3 POU class 4 homeobox 3
POU6F2 POU class 6 homeobox 2
PRKRA protein kinase, interferon-inducible double stranded RNA dependent activator
PRPH2 peripherin 2 (retinal degeneration, slow)
PRR4 proline rich 4 (lacrimal)
RABGGTA Rab geranylgeranyltransferase, alpha subunit
RABGGTB Rab geranylgeranyltransferase, beta subunit
RD3 retinal degeneration 3
RDH10 retinol dehydrogenase 10 (all-trans)
RDH12 retinol dehydrogenase 12 (all-trans/9-cis/11-cis)
RGS16 regulator of G-protein signaling 16
ROM1 retinal outer segment membrane protein 1
RP2 retinitis pigmentosa 2 (X-linked recessive)
RPE65 retinal pigment epithelium-specific protein 65kDa
RPGR retinitis pigmentosa GTPase regulator
RS1 retinoschisin 1
S100G S100 calcium binding protein G
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
SLC4A10 solute carrier family 4, sodium bicarbonate transporter, member 10
TH tyrosine hydroxylase
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
WFS1 Wolfram syndrome 1 (wolframin)
ZIC2 Zic family member 2