SCUBA

ATP6AP1 — ATPase H+ transporting accessory protein 1

ATP6AP1 belongs to a gene co-expression module in 2 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

ATP6AP1's module in each cell type

Cell typeModuleShares the module with
CD4⁺ T cellsAKT survival signaling
TCR/AP1/NFKb pathway
ABHD2, AKT1, ARL14EP, ATF7, CHD8, GNGT2, IP6K2, ITSN2 +10 moreView in SCUBA
MacrophagesER Protein Processing
Housekeeping
ACTR1A, ANXA7, ATP6AP2, ATP6V0B, ATP6V0E1, AUP1, BCAP31, BSG +41 moreView in SCUBA

About the gene

Synonyms16A, Ac45, ATP6IP1, ATP6S1, CF2, ORF, VATPS1, XAP-3, XAP3
ChromosomeX: 154428633-154436516
Predicted locationIntracellular, Membrane
Essential geneYes
Protein classDisease related genes, Essential proteins, Human disease related genes, Metabolic proteins, Plasma proteins, Potential drug targets, Predicted intracellular proteins, Predicted membrane proteins, Transporters
Biological processHydrogen ion transport, Ion transport, Transport

Function

Accessory subunit of the proton-transporting vacuolar (V)- ATPase protein pump, which is required for luminal acidification of secretory vesicles. Guides the V-type ATPase into specialized subcellular compartments, such as neuroendocrine regulated secretory vesicles or the ruffled border of the osteoclast, thereby regulating its activity. Involved in membrane trafficking and Ca(2+)-dependent membrane fusion. May play a role in the assembly of the V-type ATPase complex (Probable). In aerobic conditions, involved in intracellular iron homeostasis, thus triggering the activity of Fe(2+) prolyl hydroxylase (PHD) enzymes, and leading to HIF1A hydroxylation and subsequent proteasomal degradation. In islets of Langerhans cells, may regulate the acidification of dense-core secretory granules (By similarity).

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.