ATP6V0A2
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 12[13]
- Cytogenetic location
- 12q24.31[16]
- Expressed in
- skin of leg, sural nerve, stromal cell of endometrium, skin of abdomen, gonad, endothelial cell, body of stomach, gastric mucosa, monocyte, minor salivary glands[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- wrinkly skin syndrome[14]
- HomoloGene ID
- 56523[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en A2
en ARCL
en ARCL2A
en ATP6A2
en ATP6N1D
en ATP6V0A2
en ATPase H+ transporting V0 subunit a2
en J6B7
en RTF
en STV1
en TJ6
en TJ6M
en TJ6S
en VPH1
en WSS
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000185344
- Ensembl transcript ID
- ENST00000613625, ENST00000330342, ENST00000504192, ENST00000534943, ENST00000536426, ENST00000540368, ENST00000543687, ENST00000544833, ENST00000545059
- Entrez Gene ID
- 23545
- Exact match
- identifiers.org
- Freebase ID
- /m/03h04p5
- HGNC ID
- 18481
- HGNC gene symbol
- ATP6V0A2
- OMIM ID
- 611716
- RefSeq RNA ID
- NM_012463
- UMLS CUI
- C1425544
Press Enter · cited answer in seconds