Gene Details



CNGB3 and homologs in 1 species are found in 121 GeneSets:


- Entrez   - GeneNetwork   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Human GO 786 Genes GS195226: GO:0015075 ion transmembrane transporter activity
Expand Human 19 Genes GS219505: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_LIPOPROTEIN_METABOLISM
Expand Human 469 Genes GS222864: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_METABOLISM_OF_LIPIDS_AND_LIPOPROTEINS
Expand Tier I Human 10 Genes GS172863: HP:0000666 Horizontal nystagmus
Expand Tier I Human 124 Genes GS175492: HP:0000512 Abnormal electroretinogram
Expand Tier I Human GO 392 Genes GS199854: GO:0019001 guanyl nucleotide binding
Expand Tier I Human GO 1869 Genes GS200446: GO:0017076 purine nucleotide binding
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 414 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human GO 9 Genes GS200068: GO:0005221 intracellular cyclic nucleotide activated cation channel activity
Expand Human 40 Genes GS219610: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_GLYCEROLIPID_METABOLISM
Expand Tier I Human GO 1693 Genes GS209960: GO:0003008 system process
Expand Tier I Human GO 137 Genes GS199995: GO:0015276 ligand-gated ion channel activity
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human GO 302 Genes GS205812: GO:0022836 gated channel activity
Expand Human 37 Genes GS222851: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_LIPID_DIGESTION_MOBILIZATION_AND_TRANSPORT
Expand Tier I Human GO 392 Genes GS200393: GO:0032561 guanyl ribonucleotide binding
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 8137 Genes GS202316: GO:0050789 regulation of biological process
Expand Human 37 Genes GS219509: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_LIPID_DIGESTION_MOBILIZATION_AND_TRANSPORT
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 5436 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human GO 419 Genes GS202908: GO:0022803 passive transmembrane transporter activity
Expand Tier I Human GO 28 Genes GS203648: GO:0030551 cyclic nucleotide binding
Expand Tier I Human GO 12 Genes GS203646: GO:0030553 cGMP binding
Expand Tier I Human GO 4719 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human GO 5320 Genes GS207615: GO:0016021 integral to membrane
Expand Human 40 Genes GS222847: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_GLYCEROLIPID_METABOLISM
Expand Tier I Human 120 Genes GS171657: HP:0000613 Photophobia
Expand Tier I Human GO 2 Genes GS198430: GO:0005223 intracellular cGMP activated cation channel activity
Expand Tier I Human GO 9 Genes GS200265: GO:0043855 cyclic nucleotide-gated ion channel activity
Expand Tier I Human GO 5452 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human GO 401 Genes GS205817: GO:0022838 substrate-specific channel activity
Expand Tier III Human 10 Genes GS46983: Nicotine Dependence in Dutch Sample
Expand Tier I Human GO 2392 Genes GS206737: GO:0043168 anion binding
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human 17 Genes GS171439: HP:0000608 Macular degeneration
Expand Tier I Human 202 Genes GS171631: HP:0008051 Abnormality of the retinal pigment epithelium
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human GO 2432 Genes GS209108: GO:0000166 nucleotide binding
Expand Tier I Human GO 78 Genes GS206917: GO:0031513 nonmotile primary cilium
Expand Tier I Human GO 495 Genes GS209225: GO:0007600 sensory perception
Expand Tier I Human GO 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human GO 5400 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human GO 37 Genes GS202821: GO:0001750 photoreceptor outer segment
Expand Tier I Human GO 980 Genes GS198214: GO:0022892 substrate-specific transporter activity
Expand Tier I Human CTD 766 Genes GS124457: Mustard Gas interacting genes (MeSH:D009151) in CTD
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 22 Genes GS196170: GO:0005217 intracellular ligand-gated ion channel activity
Expand Tier I Human GO 4144 Genes GS200341: GO:0051179 localization
Expand Tier I Human GO 2433 Genes GS203886: GO:1901265 nucleoside phosphate binding
Expand Tier I Human GO 5810 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human GO 925 Genes GS197610: GO:0022857 transmembrane transporter activity
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human GO 3372 Genes GS194459: GO:0051234 establishment of localization
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 845 Genes GS198212: GO:0022891 substrate-specific transmembrane transporter activity
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Human 40 Genes GS221246: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_GLYCEROLIPID_METABOLISM
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human 398 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human 4 Genes GS174356: HP:0012043 Pendular nystagmus
Expand Tier I Human 11 Genes GS175392: HP:0011003 Severe Myopia
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 393 Genes GS196169: GO:0005216 ion channel activity
Expand Tier I Human GO 569 Genes GS209735: GO:0008324 cation transmembrane transporter activity
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human GO 1877 Genes GS201800: GO:0032553 ribonucleotide binding
Expand Tier I Human GO 302 Genes GS205816: GO:0022839 ion gated channel activity
Expand Tier I Human GO 1224 Genes GS208482: GO:0042995 cell projection
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 1236 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human GO 7689 Genes GS206623: GO:0050794 regulation of cellular process
Expand Human 37 Genes GS221076: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_LIPID_DIGESTION_MOBILIZATION_AND_TRANSPORT
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 4593 Genes GS204007: GO:0044700 single organism signaling
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human 141 Genes GS174906: HP:0000545 Myopia
Expand Human 40 Genes GS220997: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_GLYCEROLIPID_METABOLISM
Expand Tier I Human 6 Genes GS176152: HP:0001141 Severe visual impairment
Expand Tier I Human GO 205 Genes GS209987: GO:0050953 sensory perception of light stimulus
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human 66 Genes GS173753: HP:0000510 Retinitis pigmentosa
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 4983 Genes GS199124: GO:0051716 cellular response to stimulus
Expand Tier I Human GO 2625 Genes GS196343: GO:0036094 small molecule binding
Expand Tier I Human 2 Genes GS174803: HP:0007811 Horizontal pendular nystagmus
Expand Human 37 Genes GS221325: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_LIPID_DIGESTION_MOBILIZATION_AND_TRANSPORT
Expand Tier I Human GO 1862 Genes GS201794: GO:0032555 purine ribonucleotide binding
Expand Tier I Human GO 1195 Genes GS196168: GO:0005215 transporter activity
Expand Tier I Human 46 Genes GS174869: HP:0000551 Abnormality of color vision
Expand Tier III Human 19 Genes GS46981: Meta-Analysis of Nicotine Dependence in Australian and Dutch Samples
Expand Tier I Human 2 Genes GS175939: HP:0008035 Retinitis pigmentosa inversa
Expand Tier I Human GO 273 Genes GS199357: GO:0005261 cation channel activity
Expand Human 19 Genes GS220076: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_LIPOPROTEIN_METABOLISM
Expand Tier I Human GO 95 Genes GS195352: GO:0072372 primary cilium
Expand Tier I Human GO 204 Genes GS210485: GO:0007601 visual perception
Expand Tier I Human 189 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Human GO 419 Genes GS195569: GO:0015267 channel activity
Expand Tier I Human 5 Genes GS175011: HP:0007803 Monochromacy
Expand Tier I Human GO 11955 Genes GS198263: GO:0005488 binding
Expand Tier I Human GO 137 Genes GS205814: GO:0022834 ligand-gated channel activity
Expand Tier I Human 188 Genes GS171512: HP:0007703 Abnormal retinal pigmentation
Expand Tier I Human GO 4593 Genes GS206355: GO:0023052 signaling
Expand Tier I Human GO 238 Genes GS196129: GO:0005929 cilium
Expand Human 37 Genes GS220075: http://www.broadinstitute.org/gsea/msigdb/cards/REACTOME_LIPID_DIGESTION_MOBILIZATION_AND_TRANSPORT
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 4084 Genes GS209199: GO:0007165 signal transduction
Expand Tier I Human 51 Genes GS173976: HP:0001103 Abnormality of the macula
Expand Human 40 Genes GS222155: http://www.broadinstitute.org/gsea/msigdb/cards/KEGG_GLYCEROLIPID_METABOLISM
Expand Tier I Human GO 3318 Genes GS209452: GO:0006810 transport