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Protein Coding Gene : Atp6v0a2 ATPase, H+ transporting, lysosomal V0 subunit A2
Primary Identifier  MGI:104855 Organism  mouse, laboratory
Chromosome  5 NCBI Gene Number  21871
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable ATPase binding activity. Predicted to be involved in cellular response to increased oxygen levels; intracellular iron ion homeostasis; and vacuolar acidification. Predicted to act upstream of or within proton transmembrane transport. Located in acrosomal vesicle and perinuclear region of cytoplasm. Part of proton-transporting V-type ATPase, V0 domain and transmembrane transporter complex. Is expressed in several structures, including genitourinary system; hemolymphoid system gland; integumental system; sensory organ; and skeleton. Human ortholog(s) of this gene implicated in autosomal recessive cutis laxa type IIA and wrinkly skin syndrome. Orthologous to human ATP6V0A2 (ATPase H+ transporting V0 subunit a2).
  • synonyms:
  • V-ATPase a2,
  • AI385560,
  • MGI:2141277,
  • TJ6s,
  • Tj6,
  • MGI:1918750,
  • expressed sequence AI385560,
  • ATPase, H+ transporting, lysosomal (vacuolar proton pump) non-catalytic accessory protein 2 (38kD),
  • AW489264,
  • ATP6a2,
  • T-cell expressing clone j6,
  • RIKEN cDNA 8430408C20 gene,
  • ATPase, H+ transporting, lysosomal V0 subunit A2,
  • MGD-MRK-28152,
  • Atp6v0a2,
  • expressed sequence AW489264,
  • MGI:2141195,
  • MGI:2140849,
  • Atp6n2,
  • expressed sequence C76904,
  • C76904,
  • 8430408C20Rik
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Trail: ProteinCodingGene

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