Entity Details
| Primary name |
CNGA3_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q16281 |
| EntryName | CNGA3_HUMAN |
| FullName | Cyclic nucleotide-gated cation channel alpha-3 |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 694 |
| SequenceStatus | complete |
| DateCreated | 1997-11-01 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Membrane |
Domains
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| Domain | Name | Category | Type |
| IPR000595 | Cyclic nucleotide-binding domain | Domain | Domain |
| IPR005821 | Ion transport domain | Domain | Domain |
| IPR014710 | RmlC-like jelly roll fold | Family | Homologous superfamily |
| IPR018488 | Cyclic nucleotide-binding, conserved site | Site | Conserved site |
| IPR018490 | Cyclic nucleotide-binding-like | Family | Homologous superfamily |
| IPR032406 | Cyclic nucleotide-gated channel, C-terminal leucine zipper domain | Domain | Domain |
Diseases
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| Disease ID | Source | Name | Description |
| 216900 | OMIM | Achromatopsia 2 (ACHM2) | 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. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
3 interactions