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Gene: ATP10A (ATPase phospholipid transporting 10A (putative)) Homo sapiens
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Symbol: ATP10A
Name: ATPase phospholipid transporting 10A (putative)
Description: The protein encoded by this gene belongs to the family of P-type cation transport ATPases, and to the subfamily of aminophospholipid-transporting ATPases. The aminophospholipid translocases transport phosphatidylserine and phosphatidylethanolamine from one side of a bilayer to another. This gene is maternally expressed. It maps within the most common interval of deletion responsible for Angelman syndrome, also known as 'happy puppet syndrome'. [provided by RefSeq, Jul 2008]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: aminophospholipid translocase VA; ATP10C; ATPase type IV, phospholipid transporting (P-type); ATPase, class V, type 10A; ATPase, Class V, type 10C; ATPVA; ATPVC; KIAA0566; P4-ATPase flippase complex alpha subunit ATP10A; phospholipid-transporting ATPase VA; probable phospholipid-transporting ATPase VA
Orthologs:
Mus musculus (house mouse) : Atp10a (ATPase, class V, type 10A)  MGI  Alliance
Rattus norvegicus (Norway rat) : Atp10a (ATPase phospholipid transporting 10A (putative))  Alliance
Chinchilla lanigera (long-tailed chinchilla) : Atp10a (ATPase phospholipid transporting 10A (putative))
Pan paniscus (bonobo/pygmy chimpanzee) : ATP10A (ATPase phospholipid transporting 10A (putative))
Canis lupus familiaris (dog) : ATP10A (ATPase phospholipid transporting 10A (putative))
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : Atp10a (ATPase phospholipid transporting 10A (putative))
Sus scrofa (pig) : ATP10A (ATPase phospholipid transporting 10A (putative))
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381525,672,241 - 25,865,144 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371525,923,859 - 26,110,304 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361523,474,952 - 23,659,442 (-)NCBINCBI36hg18NCBI36
Build 341523,473,512 - 23,659,963NCBI
Celera154,086,178 - 4,270,059 (-)NCBI
Cytogenetic Map15q12NCBI
HuRef154,050,003 - 4,238,595 (-)NCBIHuRef
CHM1_11525,873,187 - 26,058,234 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on ATP10A
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1314601
Created: 2005-01-12
Species: Homo sapiens
Last Modified: 2019-09-12
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.