ATP6V1E1
protein-coding gene in the species Homo sapiens
Facts
14 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 22
- Cytogenetic location
- 22q11.21
- Encodes
- ATPase H+ transporting V1 subunit E1, ATPase, H+ transporting, lysosomal 31kDa, V1 subunit E isoform 1, V-type proton ATPase subunit E 1[15][16]
- Expressed in
- middle temporal gyrus, prefrontal cortex, pons, right frontal lobe, Brodmann area 9, C1 segment, cingulate gyrus, anterior cingulate cortex, Brodmann area 46, nucleus accumbens
- Found in taxon
- Homo sapiens
- Genetic association
- autosomal recessive cutis laxa type IIC
- HomoloGene ID
- 1282[3]
- Imported from
- wholeness_audit_2026-05-02
- Strand orientation
- reverse strand
🏷️ Also known as
en ARCL2C
en ATP6E
en ATP6E2
en ATP6V1E
en ATP6V1E1
en ATPase H+ transporting V1 subunit E1
en P31
en Vma4
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000131100
- Ensembl transcript ID
- ENST00000484653, ENST00000253413, ENST00000399796, ENST00000399798, ENST00000413576, ENST00000460085, ENST00000473248, ENST00000478963, ENST00000481365
- Entrez Gene ID
- 529
- Exact match
- identifiers.org
- Freebase ID
- /m/03gx2vl
- HGNC ID
- 857
- HGNC gene symbol
- ATP6V1E1
- OMIM ID
- 108746
- RefSeq RNA ID
- NM_001696, NM_001039366, NM_001039367
- UMLS CUI
- C1412677
Press Enter · cited answer in seconds
0 sources
Summary
ATP6V1E1 is a gene[1].