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Cancer Genome Characterization Initiative

Visit the database of genomic characterization data for multiple tumor types.

GO Gene List

GeneFinder Results For:Hs; sensory perception of light stimulus;
UniGene Build:Hs.234/Mm.193
[Text] [Clones]

Displaying 1 thru 225 of 225 items

SymbolNameSequence IDCGAP Gene Info
ABCA4ATP-binding cassette, sub-family A (ABC1), member 4NM_000350Gene Info
ABCC6ATP-binding cassette, sub-family C (CFTR/MRP), member 6NM_001171
NM_001079528
Gene Info
ABLIM1Actin binding LIM protein 1NM_001003408
NM_001003407
NM_002313
NM_006720
Gene Info
ABLIM1Actin binding LIM protein 1AK054890Gene Info
AIPL1Aryl hydrocarbon receptor interacting protein-like 1NM_014336
NM_001033055
NM_001033054
Gene Info
AOC2Amine oxidase, copper containing 2 (retina-specific)NM_009590
NM_001158
Gene Info
ARL6ADP-ribosylation factor-like 6NM_032146
NM_177976
Gene Info
ARR3Arrestin 3, retinal (X-arrestin)NM_004312Gene Info
ATXN7Ataxin 7NM_000333
NM_001177387
NM_001128149
Gene Info
BBS1Bardet-Biedl syndrome 1NM_024649Gene Info
BBS10Bardet-Biedl syndrome 10NM_024685Gene Info
BBS2Bardet-Biedl syndrome 2NM_031885Gene Info
BBS4Bardet-Biedl syndrome 4NM_033028
NM_001252678
Gene Info
BBS5Bardet-Biedl syndrome 5NM_152384Gene Info
BBS7Bardet-Biedl syndrome 7NM_176824
NM_018190
Gene Info
BBS9Bardet-Biedl syndrome 9NM_198428
NM_001033605
NM_001033604
NM_014451
Gene Info
BEST1Bestrophin 1NM_001139443
NM_004183
Gene Info
BFSP2Beaded filament structural protein 2, phakininNM_003571Gene Info
C2orf71Chromosome 2 open reading frame 71NM_001029883Gene Info
CABP4Calcium binding protein 4NM_145200Gene Info
CACNA1FCalcium channel, voltage-dependent, L type, alpha 1F subunitNM_005183
NM_001256789
NM_001256790
Gene Info
CACNB2Calcium channel, voltage-dependent, beta 2 subunitNM_000724
NM_201570
NM_201571
NM_201572
NM_001167945
NM_201590
NM_201596
NM_201597
NM_201593
Gene Info
CACNB4Calcium channel, voltage-dependent, beta 4 subunitNM_001005747
NM_000726
NM_001005746
NM_001145798
Gene Info
CDH23Cadherin-related 23NM_022124
NM_001171930
NM_001171933
NM_001171934
NM_001171931
NM_052836
NM_001171935
NM_001171932
NM_001171936
Gene Info
CDH3Cadherin 3, type 1, P-cadherin (placental)NM_001793Gene Info
CDHR1Cadherin-related family member 1NM_033100
NM_001171971
Gene Info
CHMChoroideremia (Rab escort protein 1)NM_000390
NM_001145414
Gene Info
CHMLChoroideremia-like (Rab escort protein 2)NM_001821Gene Info
CHRNB2Cholinergic receptor, nicotinic, beta 2 (neuronal)NM_000748Gene Info
CLDN19Claudin 19NM_001123395
NM_001185117
NM_148960
Gene Info
CLN5Ceroid-lipofuscinosis, neuronal 5NM_006493Gene Info
CLN6Ceroid-lipofuscinosis, neuronal 6, late infantile, variantNM_017882Gene Info
CLN8Ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)NM_018941Gene Info
CLRN1Clarin 1NM_001256819
NM_001195794
NM_174878
NM_052995
Gene Info
CNGA1Cyclic nucleotide gated channel alpha 1NM_001142564
NM_000087
Gene Info
CNGA3Cyclic nucleotide gated channel alpha 3NM_001298
NM_001079878
Gene Info
CNGB1Cyclic nucleotide gated channel beta 1NM_001297
NM_001135639
Gene Info
CNGB3Cyclic nucleotide gated channel beta 3NM_019098Gene Info
CNNM4Cyclin M4NM_020184Gene Info
COL11A1Collagen, type XI, alpha 1NM_080629
NM_001854
NM_001190709
NM_080630
Gene Info
COL18A1Collagen, type XVIII, alpha 1NM_030582
NM_130445
Gene Info
COL1A1Collagen, type I, alpha 1NM_000088Gene Info
COL2A1Collagen, type II, alpha 1NM_001844
NM_033150
Gene Info
CRXCone-rod homeoboxNM_000554Gene Info
CRXCone-rod homeoboxR93872Gene Info
CRXCone-rod homeoboxAF335593Gene Info
CRYAACrystallin, alpha ANM_000394Gene Info
CRYBA1Crystallin, beta A1NM_005208Gene Info
CRYBA4Crystallin, beta A4NM_001886Gene Info
CRYBB1Crystallin, beta B1NM_001887Gene Info
CRYBB2Crystallin, beta B2NM_000496Gene Info
CRYBB3Crystallin, beta B3NM_004076Gene Info
CRYGACrystallin, gamma ANM_014617Gene Info
CRYGBCrystallin, gamma BNM_005210Gene Info
CRYGCCrystallin, gamma CNM_020989Gene Info
CRYGDCrystallin, gamma DNM_006891Gene Info
CRYZCrystallin, zeta (quinone reductase)NM_001130042
NM_001889
NM_001130043
NM_001134759
Gene Info
CYP1B1Cytochrome P450, family 1, subfamily B, polypeptide 1NM_000104Gene Info
CYP4V2Cytochrome P450, family 4, subfamily V, polypeptide 2NM_207352Gene Info
DFNB31Deafness, autosomal recessive 31NM_015404
NM_001173425
NM_001083885
Gene Info
DHRS3Dehydrogenase/reductase (SDR family) member 3NM_004753Gene Info
DNAJC19DnaJ (Hsp40) homolog, subfamily C, member 19NM_001190233
NM_145261
Gene Info
EFEMP1EGF containing fibulin-like extracellular matrix protein 1NM_001039348
NM_001039349
Gene Info
EML2Echinoderm microtubule associated protein like 2NM_001193268
NM_001193269
NM_012155
Gene Info
EPAS1Endothelial PAS domain protein 1NM_001430Gene Info
ERCC6Excision repair cross-complementing rodent repair deficiency, complementation group 6NM_000124
NM_170753
Gene Info
EYA3Eyes absent homolog 3 (Drosophila)NM_001990Gene Info
EYA4Eyes absent homolog 4 (Drosophila)NM_004100
NM_172105
NM_172103
Gene Info
EYSEyes shut homolog (Drosophila)NM_001142800
NM_001142801
NM_198283
Gene Info
FAM161AFamily with sequence similarity 161, member ANM_001201543
NM_032180
Gene Info
FSCN2Fascin homolog 2, actin-bundling protein, retinal (Strongylocentrotus purpuratus)NM_001077182
NM_012418
Gene Info
FTH1Ferritin, heavy polypeptide 1NM_002032Gene Info
GABRR2Gamma-aminobutyric acid (GABA) A receptor, rho 2NM_002043Gene Info
GJA10Gap junction protein, alpha 10, 62kDaNM_032602Gene Info
GJA3Gap junction protein, alpha 3, 46kDaNM_021954Gene Info
GJA8Gap junction protein, alpha 8, 50kDaNM_005267Gene Info
GJC1Gap junction protein, gamma 1, 45kDaNM_005497
NM_001080383
Gene Info
GJD2Gap junction protein, delta 2, 36kDaNM_020660Gene Info
GLRA1Glycine receptor, alpha 1NM_001146040
NM_000171
Gene Info
GLRBGlycine receptor, betaNM_000824
NM_001166060
NM_001166061
Gene Info
GNAT1Guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 1NM_144499
NM_000172
Gene Info
GNAT2Guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2NM_005272Gene Info
GPR143G protein-coupled receptor 143NM_000273Gene Info
GPR179G protein-coupled receptor 179NM_001004334Gene Info
GPR98G protein-coupled receptor 98NM_032119Gene Info
GRK1G protein-coupled receptor kinase 1NM_002929Gene Info
GRK1G protein-coupled receptor kinase 1BX647503Gene Info
GRK7G protein-coupled receptor kinase 7NM_139209Gene Info
GRM6Glutamate receptor, metabotropic 6NM_000843Gene Info
GRM8Glutamate receptor, metabotropic 8NM_001127323
NM_000845
Gene Info
GUCA1AGuanylate cyclase activator 1A (retina)NM_000409Gene Info
GUCA1BGuanylate cyclase activator 1B (retina)NM_002098Gene Info
GUCA1CGuanylate cyclase activator 1CNM_005459Gene Info
GUCY2DGuanylate cyclase 2D, membrane (retina-specific)NM_000180Gene Info
GUCY2FGuanylate cyclase 2F, retinalNM_001522Gene Info
HMCN1Hemicentin 1NM_031935Gene Info
HPS1Hermansky-Pudlak syndrome 1NM_000195
NM_182639
Gene Info
IMPG1Interphotoreceptor matrix proteoglycan 1NM_001563Gene Info
IMPG2Interphotoreceptor matrix proteoglycan 2NM_016247Gene Info
IQCB1IQ motif containing B1NM_001023570
NM_001023571
Gene Info
SymbolNameSequence IDCGAP Gene Info
IRX5Iroquois homeobox 5NM_005853
NM_001252197
Gene Info
KCNJ10Potassium inwardly-rectifying channel, subfamily J, member 10NM_002241Gene Info
KERAKeratocanNM_007035Gene Info
KIFC3Kinesin family member C3NM_001130100
NM_005550
NM_001130099
Gene Info
KRT12Keratin 12NM_000223Gene Info
LAMB2Laminin, beta 2 (laminin S)NM_002292Gene Info
LAMC3Laminin, gamma 3NM_006059Gene Info
LRATLecithin retinol acyltransferase (phosphatidylcholine--retinol O-acyltransferase)NM_004744Gene Info
LUMLumicanNM_002345Gene Info
MAKMale germ cell-associated kinaseNM_001242957
NM_005906
NM_001242385
Gene Info
MIPMajor intrinsic protein of lens fiberNM_012064Gene Info
MKKSMcKusick-Kaufman syndromeNM_018848
NM_170784
Gene Info
MYO3AMyosin IIIANM_017433Gene Info
MYO3BMyosin IIIBNM_138995
NM_001083615
Gene Info
MYO5AMyosin VA (heavy chain 12, myoxin)NM_000259
NM_001142495
Gene Info
MYO7AMyosin VIIANM_000260
NM_001127180
NM_001127179
Gene Info
MYO9AMyosin IXANM_006901Gene Info
NDPNorrie disease (pseudoglioma)NM_000266Gene Info
NPHP3Nephronophthisis 3 (adolescent)NM_153240Gene Info
NR2E1Nuclear receptor subfamily 2, group E, member 1NM_003269Gene Info
NR2E3Nuclear receptor subfamily 2, group E, member 3NM_016346
NM_014249
Gene Info
NRLNeural retina leucine zipperNM_006177Gene Info
NYXNyctalopinNM_022567Gene Info
OATOrnithine aminotransferaseNM_000274
NM_001171814
Gene Info
OCLMOculomedinNM_022375Gene Info
OPA1Optic atrophy 1 (autosomal dominant)NM_130837
NM_130836
NM_130835
NM_130834
NM_130833
NM_015560
NM_130832
NM_130831
Gene Info
OPA3Optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)NM_025136
NM_001017989
Gene Info
OPN1LWOpsin 1 (cone pigments), long-wave-sensitiveNM_020061Gene Info
OPN1MWOpsin 1 (cone pigments), medium-wave-sensitiveNM_000513Gene Info
OPN1MW2Opsin 1 (cone pigments), medium-wave-sensitive 2NM_001048181Gene Info
OPN1SWOpsin 1 (cone pigments), short-wave-sensitiveNM_001708Gene Info
OPN3Opsin 3NM_014322Gene Info
OPN4Opsin 4NM_001030015
NM_033282
Gene Info
OPN5Opsin 5NM_181744Gene Info
PAX2Paired box 2NM_003988
NM_003987
NM_003990
NM_000278
NM_003989
Gene Info
PAX6Paired box 6NM_000280
NM_001258462
NM_001604
NM_001127612
NM_001258464
NM_001258463
NM_001258465
Gene Info
PCDH15Protocadherin-related 15NM_001142771
NM_001142772
NM_001142763
NM_001142764
NM_033056
NM_001142766
NM_001142768
NM_001142773
NM_001142767
NM_001142765
NM_001142770
NM_001142769
Gene Info
PDCPhosducinNM_002597
NM_022576
Gene Info
PDCLPhosducin-likeNM_005388Gene Info
PDE6APhosphodiesterase 6A, cGMP-specific, rod, alphaNM_000440Gene Info
PDE6BPhosphodiesterase 6B, cGMP-specific, rod, betaBC039412Gene Info
PDE6BPhosphodiesterase 6B, cGMP-specific, rod, betaNM_000283
NM_001145291
NM_001145292
Gene Info
PDE6CPhosphodiesterase 6C, cGMP-specific, cone, alpha primeNM_006204Gene Info
PDE6DPhosphodiesterase 6D, cGMP-specific, rod, deltaNM_002601Gene Info
PDE6GPhosphodiesterase 6G, cGMP-specific, rod, gammaNM_002602Gene Info
PDE6HPhosphodiesterase 6H, cGMP-specific, cone, gammaNM_006205Gene Info
PITPNAPhosphatidylinositol transfer protein, alphaNM_006224Gene Info
POU4F3POU class 4 homeobox 3NM_002700Gene Info
POU6F2POU class 6 homeobox 2NM_007252
NM_001166018
Gene Info
PPEF2Protein phosphatase, EF-hand calcium binding domain 2NM_006239Gene Info
PPT1Palmitoyl-protein thioesterase 1NM_000310
NM_001142604
Gene Info
PRCDProgressive rod-cone degenerationNM_001077620Gene Info
PRCDProgressive rod-cone degenerationAK054729Gene Info
PROM1Prominin 1NM_001145847
NM_006017
NM_001145848
NM_001145849
NM_001145850
NM_001145851
NM_001145852
Gene Info
PRPH2Peripherin 2 (retinal degeneration, slow)NM_000322Gene Info
PRR4Proline rich 4 (lacrimal)NM_007244
NM_001098538
Gene Info
RABGGTARab geranylgeranyltransferase, alpha subunitNM_004581
NM_182836
Gene Info
RABGGTBRab geranylgeranyltransferase, beta subunitNM_004582Gene Info
RAXRetina and anterior neural fold homeoboxNM_013435Gene Info
RAX2Retina and anterior neural fold homeobox 2NM_032753Gene Info
RBP3Retinol binding protein 3, interstitialNM_002900Gene Info
RBP4Retinol binding protein 4, plasmaNM_006744Gene Info
RCVRNRecoverinNM_002903Gene Info
RD3Retinal degeneration 3NM_183059
NM_001164688
Gene Info
RDH10Retinol dehydrogenase 10 (all-trans)NM_172037Gene Info
RDH12Retinol dehydrogenase 12 (all-trans/9-cis/11-cis)NM_152443Gene Info
RDH5Retinol dehydrogenase 5 (11-cis/9-cis)NM_001199771
NM_002905
Gene Info
RDH8Retinol dehydrogenase 8 (all-trans)NM_015725Gene Info
RGRRetinal G protein coupled receptorNM_002921
NM_001012720
NM_001012722
Gene Info
RGS16Regulator of G-protein signaling 16NM_002928Gene Info
RGS9Regulator of G-protein signaling 9NM_003835
NM_001081955
NM_001165933
Gene Info
RGS9BPRegulator of G protein signaling 9 binding proteinNM_207391Gene Info
RHORhodopsinNM_000539Gene Info
RIMS1Regulating synaptic membrane exocytosis 1NM_014989
NM_001168407
NM_001168410
NM_001168408
NM_001168409
NM_001168411
Gene Info
RLBP1Retinaldehyde binding protein 1NM_000326Gene Info
ROM1Retinal outer segment membrane protein 1NM_000327Gene Info
RORBRAR-related orphan receptor BNM_006914Gene Info
RP1Retinitis pigmentosa 1 (autosomal dominant)NM_006269Gene Info
RP1L1Retinitis pigmentosa 1-like 1NM_178857Gene Info
RP2Retinitis pigmentosa 2 (X-linked recessive)NM_006915Gene Info
RPE65Retinal pigment epithelium-specific protein 65kDaNM_000329Gene Info
RPGRRetinitis pigmentosa GTPase regulatorNM_001034853
NM_000328
Gene Info
RPGRIP1Retinitis pigmentosa GTPase regulator interacting protein 1NM_020366Gene Info
RRHRetinal pigment epithelium-derived rhodopsin homologNM_006583Gene Info
RS1Retinoschisin 1NM_000330Gene Info
SAGS-antigen; retina and pineal gland (arrestin)NM_000541Gene Info
SDR16C5Short chain dehydrogenase/reductase family 16C, member 5NM_138969Gene Info
SFRP5Secreted frizzled-related protein 5NM_003015Gene Info
SIX3SIX homeobox 3NM_005413Gene Info
SIX6SIX homeobox 6NM_007374Gene Info
SLC24A1Solute carrier family 24 (sodium/potassium/calcium exchanger), member 1NM_004727
NM_001254740
Gene Info
SLC24A2Solute carrier family 24 (sodium/potassium/calcium exchanger), member 2NM_020344
NM_001193288
Gene Info
SLC24A2Solute carrier family 24 (sodium/potassium/calcium exchanger), member 2DQ067464Gene Info
SLC24A2Solute carrier family 24 (sodium/potassium/calcium exchanger), member 2BP309913
BP309946
Gene Info
SLC45A2Solute carrier family 45, member 2NM_001012509
NM_016180
Gene Info
SPATA7Spermatogenesis associated 7NM_018418
NM_001040428
Gene Info
TACSTD2Tumor-associated calcium signal transducer 2NM_002353Gene Info
TGFBITransforming growth factor, beta-induced, 68kDaNM_000358Gene Info
THTyrosine hydroxylaseNM_199292
NM_199293
NM_000360
Gene Info
TIMP3TIMP metallopeptidase inhibitor 3NM_000362Gene Info
SymbolNameSequence IDCGAP Gene Info
TRPM1Transient receptor potential cation channel, subfamily M, member 1NM_001252020
NM_001252024
NM_002420
NM_001252030
Gene Info
TULP1Tubby like protein 1NM_003322Gene Info
TULP2Tubby like protein 2NM_003323Gene Info
TYRTyrosinase (oculocutaneous albinism IA)NM_000372Gene Info
UNC119Unc-119 homolog (C. elegans)NM_054035
NM_005148
Gene Info
USH1CUsher syndrome 1C (autosomal recessive, severe)NM_153676
NM_005709
Gene Info
USH1GUsher syndrome 1G (autosomal recessive)NM_173477Gene Info
USH2AUsher syndrome 2A (autosomal recessive, mild)NM_206933
NM_007123
Gene Info
VAX2Ventral anterior homeobox 2NM_012476Gene Info
VSX1Visual system homeobox 1NM_001256272
NM_014588
NM_001256271
NM_199425
Gene Info
VSX2Visual system homeobox 2NM_182894Gene Info
WDR36WD repeat domain 36NM_139281Gene Info
WFS1Wolfram syndrome 1 (wolframin)NM_006005
NM_001145853
Gene Info
WFS1Wolfram syndrome 1 (wolframin)AK295986Gene Info
ZIC2Zic family member 2NM_007129Gene Info
ZNF513Zinc finger protein 513NM_144631
NM_001201459
Gene Info
-Transcribed locusBG426037Gene Info
-Transcribed locusDB309144Gene Info
-Transcribed locusBE221553Gene Info
-Transcribed locusBQ775109Gene Info
-Transcribed locus, strongly similar to NP_001152854.1 gap junction gamma-1 protein [Mus musculus]CR933719Gene Info
-Transcribed locusCA944687Gene Info
-Transcribed locus, strongly similar to NP_001034437.1 EGF-containing fibulin-like extracellular matrix protein 1 precursor [Homo sapiens]AL603118Gene Info
-Transcribed locusBM724663Gene Info
-Transcribed locus, strongly similar to NP_766606.2 unconventional myosin-IXa [Mus musculus]AI539366Gene Info