OPN1SW
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 7[12]
- Cytogenetic location
- 7q32.1[15]
- Expressed in
- sural nerve, Brodmann area 46, stromal cell of endometrium, retinal pigment epithelium, Achilles tendon, Descending thoracic aorta, apex of heart, prefrontal cortex, ganglionic eminence, exocrine gland[16][17][18][19][20][21][22][23][24][25]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- tritanopia[13]
- HomoloGene ID
- 1291[3]
- Strand orientation
- reverse strand[14]
🏷️ Also known as
en BCP
en BOP
en CBT
en OPN1SW
en opsin 1 (cone pigments), short-wave-sensitive
en opsin 1, short wave sensitive
🔖 Identifiers · 11
- Image (Wikimedia Commons)
- OPN1SW.png ↗
- Ensembl gene ID
- ENSG00000128617
- Ensembl transcript ID
- ENST00000249389
- Entrez Gene ID
- 611
- Exact match
- identifiers.org
- Freebase ID
- /m/03d309d
- HGNC ID
- 1012
- HGNC gene symbol
- OPN1SW
- OMIM ID
- 613522
- RefSeq RNA ID
- NM_001708, NM_001385125
- UMLS CUI
- C1412770
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