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MIRAGE
Retinal guanylyl cyclase 1
Summary
- UniProt ID
- Q02846
- Gene Symbol
-
- CORD6
- GUC1A4
- GUC2D
- GUCY2D
- RETGC
- RETGC1
- Gene ID
- 3000
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- Q02846
- PubChem
- Q02846
- The Human Metabolome Database
- HMDBP01067
- The O-GlcNAc Database
- Q02846
- Re-Glyco
- Q02846
Annotation
- Keyword
-
- Cell projection
- Cone-rod dystrophy
- Congenital stationary night blindness
- Disease variant
- Disulfide bond
- Endoplasmic reticulum
- GTP-binding
- Glycoprotein
- Leber congenital amaurosis
- Lyase
- Reference proteome
- Signal
- Transmembrane helix
- Vision
- cGMP biosynthesis
- Gene Ontology (GO)
Sequence
MTACARRAGGLPDPGLCGPAWWAPSLPRLPRALPRLPLLLLLLLLQPPALSAVFTVGVLGPWACDPIFSRARPDLAARLAAARLNRDPGLAGGPRFEVALLPEPCRTPGSLGAVSSALARVSGLVGPVNPAACRPAELLAEEAGIALVPWGCPWTQAEGTTAPAVTPAADALYALLRAFGWARVALVTAPQDLWVEAGRSLSTALRARGLPVASVTSMEPLDLSGAREALRKVRDGPRVTAVIMVMHSVLLGGEEQRYLLEAAEELGLTDGSLVFLPFDTIHYALSPGPEALAALANSSQLRRAHDAVLTLTRHCPSEGSVLDSLRRAQERRELPSDLNLQQVSPLFGTIYDAVFLLARGVAEARAAAGGRWVSGAAVARHIRDAQVPGFCGDLGGDEEPPFVLLDTDAAGDRLFATYMLDPARGSFLSAGTRMHFPRGGSAPGPDPSCWFDPNNICGGGLEPGLVFLGFLLVVGMGLAGAFLAHYVRHRLLHMQMVSGPNKIILTVDDITFLHPHGGTSRKVAQGSRSSLGARSMSDIRSGPSQHLDSPNIGVYEGDRVWLKKFPGDQHIAIRPATKTAFSKLQELRHENVALYLGLFLARGAEGPAALWEGNLAVVSEHCTRGSLQDLLAQREIKLDWMFKSSLLLDLIKGIRYLHHRGVAHGRLKSRNCIVDGRFVLKITDHGHGRLLEAQKVLPEPPRAEDQLWTAPELLRDPALERRGTLAGDVFSLAIIMQEVVCRSAPYAMLELTPEEVVQRVRSPPPLCRPLVSMDQAPVECILLMKQCWAEQPELRPSMDHTFDLFKNINKGRKTNIIDSMLRMLEQYSSNLEDLIRERTEELELEKQKTDRLLTQMLPPSVAEALKTGTPVEPEYFEQVTLYFSDIVGFTTISAMSEPIEVVDLLNDLYTLFDAIIGSHDVYKVETIGDAYMVASGLPQRNGQRHAAEIANMSLDILSAVGTFRMRHMPEVPVRIRIGLHSGPCVAGVVGLTMPRYCLFGDTVNTASRMESTGLPYRIHVNLSTVGILRALDSGYQVELRGRTELKGKGAEDTFWLVGRRGFNKPIPKPPDLQPGSSNHGISLQEIPPERRRKLEKARPGQFS
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 166 |
|
|
||
| 297 | N-linked (GlcNAc...) asparagine |
|
||
| 926 |
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Inactivation, recovery and regulation of the phototransduction cascade | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050534 | congenital stationary night blindness | |
| DOID:0110078 | Leber congenital amaurosis 1 | |
| DOID:0111011 | cone-rod dystrophy 6 | |
| DOID:10584 | retinitis pigmentosa | |
| DOID:980 | choroidal sclerosis |
