Entity Details

Primary name CNGB3_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ9NQW8
EntryNameCNGB3_HUMAN
FullNameCyclic nucleotide-gated cation channel beta-3
TaxID9606
Evidenceevidence at protein level
Length809
SequenceStatuscomplete
DateCreated2004-03-29
DateModified2021-06-02

Ontological Relatives

GenesCNGB3

GO terms

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GOName
GO:0001750 photoreceptor outer segment
GO:0005222 intracellular cAMP-activated cation channel activity
GO:0005223 intracellular cGMP-activated cation channel activity
GO:0006812 cation transport
GO:0007165 signal transduction
GO:0007601 visual perception
GO:0030553 cGMP binding
GO:1902495 transmembrane transporter complex

Subcellular Location

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Subcellular Location
Membrane

Domains

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DomainNameCategoryType
IPR000595 Cyclic nucleotide-binding domainDomainDomain
IPR014710 RmlC-like jelly roll foldFamilyHomologous superfamily
IPR018488 Cyclic nucleotide-binding, conserved siteSiteConserved site
IPR018490 Cyclic nucleotide-binding-likeFamilyHomologous superfamily
IPR032943 Cyclic nucleotide-gated cation channel beta-3FamilyFamily

Diseases

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Disease IDSourceNameDescription
248200 OMIMStargardt disease 1 (STGD1)A common hereditary macular degeneration. It is characterized by decreased central vision, atrophy of the macula and underlying retinal pigment epithelium, and frequent presence of prominent flecks in the posterior pole of the retina. The disease is caused by variants affecting the gene represented in this entry.
262300 OMIMAchromatopsia 3 (ACHM3)An autosomal recessive, ocular stationary disorder due to the absence of functioning cone photoreceptors in the retina. It is characterized by total colorblindness, low visual acuity, photophobia and nystagmus. Achromatopsia type 3 patients manifest severe myopia. The disease is caused by variants affecting the gene represented in this entry.

Interactions

1 interaction

InteractorPartnerSourcesPublicationsLink
CNGB3_HUMANCNGA3_HUMANBioGRID15223812 details