Sequence Detail

ID/Version

O70228 Q922L9 Q8VDI5 (UniProt | EBI)

Last sequence update: 2009-05-05
Last annotation update: 2025-02-05

Sequence description from provider

RecName: Full=Probable phospholipid-transporting ATPase IIA; EC=7.6.2.1 {ECO:0000250|UniProtKB:O75110};AltName: Full=ATPase class II type 9A;

Provider

SWISS-PROT

Sequence

Polypeptide 1047 aa

Source

Organism mouse

See UniProt | EBI for source

Annotated genes and markers

Follow the symbol links to get more information on the GO terms, expression assays, orthologs, phenotypic alleles, and other information for the genes or markers below.

Type	Symbol	Name	GO Terms	Expression Assays	Orthologs	Phenotypic Alleles
Gene	Atp9a	ATPase, class II, type 9A	37	101	2	25

Sequence references in MGI

J:47134 Halleck MS, et al., Multiple members of a third subfamily of P-type ATPases identified by genomic sequences and ESTs. Genome Res. 1998 Apr;8(4):354-61
J:59384 Halleck MS, et al., Differential expression of putative transbilayer amphipath transporters. Physiol Genomics. 1999 Nov 11;1(3):139-50
J:292518 Huttlin EL, et al., A tissue-specific atlas of mouse protein phosphorylation and expression. Cell. 2010 Dec 23;143(7):1174-89
J:335674 Meng T, et al., ATP9A deficiency causes ADHD and aberrant endosomal recycling via modulating RAB5 and RAB11 activity. Mol Psychiatry. 2023 Mar;28(3):1219-1231