ATP13A2
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 1[13]
- Cytogenetic location
- 1p36.13[17]
- Encodes
- ATPase cation transporting 13A2, Cation-transporting ATPase, Probable cation-transporting ATPase 13A2[9][10][11]
- Expressed in
- right frontal lobe, right hemisphere of cerebellum, prefrontal cortex, anterior cingulate cortex, pons, Brodmann area 9, anterior pituitary, amygdala, hypothalamus, nucleus accumbens[18][19][20][21][22][23][24][25][26][27]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- Kufor-Rakeb syndrome, spastic paraplegia 78, autosomal recessive; SPG78[14][15]
- HomoloGene ID
- 56940[3]
- Strand orientation
- reverse strand[16]
🏷️ Also known as
en ATP13A2
en ATPase 13A2
en ATPase cation transporting 13A2
en CLN12
en HSA9947
en KRPPD
en PARK9
en SPG78
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000159363
- Ensembl transcript ID
- ENST00000326735, ENST00000341676, ENST00000452699, ENST00000463860, ENST00000466561, ENST00000502418, ENST00000502860, ENST00000503552, ENST00000506174, ENST00000508222, ENST00000509392, ENST00000509619, ENST00000510069, ENST00000511957
- Entrez Gene ID
- 23400
- Exact match
- identifiers.org
- Freebase ID
- /m/03gys81
- HGNC ID
- 30213
- HGNC gene symbol
- ATP13A2
- OMIM ID
- 610513
- RefSeq RNA ID
- XM_011541129, NM_001141973, NM_001141974, NM_022089, XM_005245810, XM_005245811, XM_005245812, XM_005245815, XM_006710512, XM_006710513, XM_011541128, XM_017000844, XM_017000845, XM_017000846, XM_017000847, XM_017000848, XM_017000849, XM_017000850
- UMLS CUI
- C1540215
🔗 Connections
Expressed in 8
Chromosome 1
Found in taxon 1
Genetic association 1
Instance of 1
← Genetic association 1
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Summary
ATP13A2 is a gene[1].