ATPase H+ transporting V0 subunit a2

Summary
Gene Symbol
  • ATP6V0A2
Aliases
  • ATP6N1D
  • ATP6a2
  • J6B7
  • RTF
  • Stv1
  • TJ6
  • TJ6M
  • TJ6s
  • V-ATPase subunit a2
  • V-type proton ATPase 116 kDa subunit a2
  • Vph1
  • a2
  • a2V
  • infantile malignant osteopetrosis
  • regeneration and tolerance factor
Organism
Homo sapiens (human)
External Links
NCBI Gene
23545
HGNC
18481
KEGG Gene ID
hsa:23545
PubChem
23545
Alliance of Genome Resources
Annotation
Keyword
  • Cell membrane
  • Endosome
  • Glycoprotein
  • Hydrogen ion transport
  • Phosphoprotein
  • Reference proteome
  • Transmembrane helix
Proteins
Displaying 1 entry
UniProt Protein Name
Q9Y487
  • Lysosomal H(+)-transporting ATPase V0 subunit a 2
  • TJ6
  • Vacuolar proton translocating ATPase 116 kDa subunit a isoform 2
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
GO Hierarchy
Human Protein Atlas
ENSG00000185344

soft tissue soft tissue blood blood blood blood blood blood blood blood blood blood blood blood blood blood lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node kidney kidney adrenal gland adrenal gland breast breast duodenum stomach small intestine colon rectum appendix esophagus eye eye salivary gland nasopharynx nasopharynx tongue tonsil tonsil tonsil hair skin adipose tissue adipose tissue adipose tissue spinal cord oral mucosa lung lung heart bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus liver pancreas thyroid gland parathyroid gland parathyroid gland parathyroid gland parathyroid gland parathyroid gland spleen gallbladder ductus deferens ductus deferens seminal vesicle seminal vesicle seminal vesicle seminal vesicle testis testis epididymis epididymis brain smooth muscle urinary bladder prostate bone marrow skeletal muscle skeletal muscle skeletal muscle skeletal muscle skeletal muscle thymus thymus cartilage sole of foot sole of foot soft tissue blood blood blood blood blood blood blood blood blood blood blood blood lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lymph node lactating breast lactating breast kidney kidney adrenal gland adrenal gland duodenum stomach small intestine colon rectum appendix esophagus eye eye salivary gland salivary gland salivary gland salivary gland salivary gland salivary gland nasopharynx tongue tonsil tonsil hair skin adipose tissue adipose tissue adipose tissue adipose tissue adipose tissue adipose tissue adipose tissue spinal cord oral mucosa lung lung heart bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus bronchus liver pancreas thyroid gland parathyroid gland parathyroid gland parathyroid gland parathyroid gland parathyroid gland spleen gallbladder brain skeletal muscle skeletal muscle skeletal muscle skeletal muscle skeletal muscle thymus thymus smooth muscle urinary bladder vagina ovary ovary fallopian tube fallopian tube endometrium placenta cervix cervix bone marrow cartilage sole of foot sole of foot olfactory region cerebral cortex cerebellum medulla pons midbrain pituitary gland hypothalamus amygdala thalamus choroid plexus choroid plexus corpus callosum basal ganglia substantia nigra dorsal raphe dorsal raphe dorsal raphe dorsal raphe dorsal raphe dorsal raphe caudate hippocampus retina retina

Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.

KEGG BRITE Database
Orthology
K02154
Name
V-type H+-transporting ATPase subunit a
References
Disease
Disease Ontology
Displaying entries 41 - 50 of 121 in total
DO ID Disease Name Source
DOID:0090132 complex cortical dysplasia with other brain malformations 7
DOID:0090137 complex cortical dysplasia with other brain malformations 1
DOID:0110096 short-rib thoracic dysplasia 14 with polydactyly
DOID:0110892 inflammatory bowel disease 1
DOID:0110942 autosomal recessive osteopetrosis 1
DOID:0110946 autosomal recessive osteopetrosis 7
DOID:0111045 platelet-type bleeding disorder 9
DOID:0111056 platelet-type bleeding disorder 3
DOID:0111057 platelet-type bleeding disorder 11
DOID:0111135 congenital generalized lipodystrophy type 1
The Human Phenotype Ontology
Displaying entries 41 - 50 of 114 in total
HPO ID HPO Term
HP:0001320 Cerebellar vermis hypoplasia
HP:0001321 Cerebellar hypoplasia
HP:0001339 Lissencephaly
HP:0001350 Slurred speech
HP:0001374 Congenital hip dislocation
HP:0001382 Joint hypermobility
HP:0001476 Delayed closure of the anterior fontanelle
HP:0001508 Failure to thrive
HP:0001511 Intrauterine growth retardation
HP:0001537 Umbilical hernia
Displaying all 4 entries
Disease ID Disease Name
OMIM:219200
  • autosomal recessive cutis laxa type 2A
ORPHA:357074
  • autosomal recessive cutis laxa type 2, classic type
OMIM:278250
  • wrinkly skin syndrome
ORPHA:2834
  • wrinkly skin syndrome

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Last updated: August 19, 2024