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Standards Ontologies Notations
ATPase 13A3

Summary
Gene Symbol
  • ATP13A3
Organism
Homo sapiens (human)
NCBI Gene
79572
PubChem
79572
Alliance of Genome Resources
Annotation
Keyword
  • ATP-binding
  • Alternative splicing
  • Endosome
  • Magnesium
  • Metal-binding
  • Phosphoprotein
  • Proteomics identification
  • Reference proteome
  • Translocase
  • Transmembrane helix
Proteins
Displaying all 2 entries
UniProt Protein Name
Q9H7F0
  • ATPase family homolog up-regulated in senescence cells 1
  • Putrescine transporting ATPase
A0A2R8Y635
Annotation information from UniProt.
Gene Ontology (GO)
Displaying all 4 entries
GO Term Evidence Code PMID
monoatomic cation transmembrane transport
polyamine transmembrane transport
putrescine transport
intracellular calcium ion homeostasis
GO Hierarchy
Displaying entries 1 - 5 of 8 in total
GO Term Evidence Code PMID
ATP hydrolysis activity
P-type ion transporter activity
metal ion binding
ABC-type putrescine transporter activity
ATP binding
GO Hierarchy
Gene Ontology information from NCBI Gene and UniProt.
OrthoDB (Group)
Group level
Eukaryota
Group Name
transporter
Functional Category
  • G: Carbohydrate transport and metabolism
  • J: Translation, ribosomal structure and biogenesis
  • T: Signal transduction mechanisms
Displaying all 6 entries
Gene Ontology
ATP binding
ATPase-coupled monoatomic cation transmembrane transporter activity
P-type ion transporter activity
P-type transmembrane transporter activity
intracellular calcium ion homeostasis
nucleotide binding
Displaying all 9 entries
InterPro
HAD superfamily
HAD-like superfamily
P-type ATPase, A domain superfamily
P-type ATPase, cytoplasmic domain N
P-type ATPase, haloacid dehalogenase domain
P-type ATPase, phosphorylation site
P-type ATPase, subfamily V
P-type ATPase, transmembrane domain superfamily
P-type ATPase
Disease
Disease Ontology
Displaying all 7 entries
DO ID Disease Name Source
DOID:0060556 Kufor-Rakeb syndrome
DOID:0060893 juvenile-onset Parkinson's disease
DOID:14330 Parkinson's disease
DOID:14503 neuronal ceroid lipofuscinosis
DOID:14557 primary pulmonary hypertension
DOID:2476 hereditary spastic paraplegia
DOID:332 amyotrophic lateral sclerosis
Ortholog
Displaying entries 1 - 10 of 93 in total
Species Gene ID OrthoDB Alliance of Genome Resources Orthologous MAtrix
177664 WB:WBGene00022010
177822 WB:WBGene00012341
224088 MGI:2685387 MOUSE19299
317815 FB:FBgn0052000
360728 RGD:1590881
471045 9598_0:00133e PANTR32966
478607 CANLF13423
523889 BOVIN14754
572029 ZFIN:ZDB-GENE-120521-1
678704 RATNO04199
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024