ATPase cation transporting 13A2

Summary
Gene Symbol
  • ATP13A2
Organism
Homo sapiens (human)
NCBI Gene
23400
PubChem
23400
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • ATP-binding
  • Alternative splicing
  • Cytoplasmic vesicle
  • Disease variant
  • Endosome
  • Glycoprotein
  • Hereditary spastic paraplegia
  • Lipid-binding
  • Lysosome
  • Magnesium
  • Metal-binding
  • Neuronal ceroid lipofuscinosis
  • Parkinsonism
  • Phosphoprotein
  • Reference proteome
  • Translocase
  • Transmembrane helix
  • Transport
Proteins
Displaying all 3 entries
UniProt Protein Name
Q8NBS1
Q9NQ11
Q8N4D4
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
GO Hierarchy
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:0112348 hereditary spastic paraplegia 78
DOID:14330 Parkinson's disease
DOID:14503 neuronal ceroid lipofuscinosis
DOID:2476 hereditary spastic paraplegia
DOID:332 amyotrophic lateral sclerosis

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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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