ATP6AP1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human X chromosome[13]
- Cytogenetic location
- Xq28[16]
- Expressed in
- Brodmann area 10, paraflocculus of cerebellum, islet of Langerhans, stromal cell of endometrium, right hemisphere of cerebellum, right frontal lobe, anterior pituitary, frontal pole, middle frontal gyrus, cingulate gyrus[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- immunodeficiency 47[14]
- HomoloGene ID
- 914[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en 16A
en Ac45
en ATP6AP1
en ATP6IP1
en ATP6S1
en ATPase H+ transporting accessory protein 1
en CF2
en VATPS1
en XAP-3
en XAP3
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000071553
- Ensembl transcript ID
- ENST00000619046, ENST00000369762, ENST00000422890, ENST00000429585, ENST00000439372, ENST00000446552, ENST00000449556, ENST00000455205, ENST00000484908, ENST00000491569, ENST00000677342, ENST00000677332, ENST00000678317, ENST00000679241
- Entrez Gene ID
- 537
- Exact match
- identifiers.org
- Freebase ID
- /m/03gy5s0
- HGNC ID
- 868
- HGNC gene symbol
- ATP6AP1
- Microsoft Academic ID (discontinued)
- 2779832556
- OMIM ID
- 300197
- RefSeq RNA ID
- NM_001183
- UMLS CUI
- C1412687
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Summary
ATP6AP1 is a gene[1].