OPN1MW
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human X chromosome[14]
- Cytogenetic location
- Xq28[17]
- Expressed in
- testicle, appendix, blood, urinary bladder, myometrium, left adrenal cortex, coronary artery, left coronary artery, right auricle of heart, stomach[18][19][20][21][22][23][24][25][26][27]
- Found in taxon
- Homo sapiens[13]
- Genetic association
- green color blindness[15]
- HomoloGene ID
- 88332[3]
- Strand orientation
- forward strand[16]
🏷️ Also known as
en CBBM
en CBD
en COD5
en GCP
en GOP
en OPN1MW
en OPN1MW1
en opsin 1 (cone pigments), medium-wave-sensitive
en opsin 1, medium wave sensitive
🔖 Identifiers · 12
- Image (Wikimedia Commons)
- OPN1MW.png ↗
- Ensembl gene ID
- ENSG00000268221
- Ensembl transcript ID
- ENST00000595290, ENST00000596998, ENST00000595330
- Entrez Gene ID
- 2652
- Exact match
- identifiers.org
- Freebase ID
- /m/03d8cfj
- HGNC ID
- 4206
- HGNC gene symbol
- OPN1MW
- Microsoft Academic ID (discontinued)
- 2780225373
- OMIM ID
- 300821
- RefSeq RNA ID
- NM_000513
- UMLS CUI
- C1415024
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Summary
OPN1MW is a gene[1].