Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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23250 |
Gene nameGene Name - the full gene name approved by the HGNC.
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ATPase phospholipid transporting 11A |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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ATP11A |
SynonymsGene synonyms aliases
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ATPIH, ATPIS |
ChromosomeChromosome number
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13 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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13q34 |
SummarySummary of gene provided in NCBI Entrez Gene.
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The protein encoded by this gene is an integral membrane ATPase. The encoded protein is probably phosphorylated in its intermediate state and likely drives the transport of ions such as calcium across membranes. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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UniProt ID |
P98196 |
Protein name |
Phospholipid-transporting ATPase IH (EC 7.6.2.1) (ATPase IS) (ATPase class VI type 11A) (P4-ATPase flippase complex alpha subunit ATP11A) |
Protein function |
Catalytic component of a P4-ATPase flippase complex which catalyzes the hydrolysis of ATP coupled to the transport of aminophospholipids, phosphatidylserines (PS) and phosphatidylethanolamines (PE), from the outer to the inner leaflet of the plasma membrane (PubMed:25315773, PubMed:25947375, PubMed:26567335, PubMed:29799007, PubMed:30018401). Contributes to the maintenance of membrane lipid asymmetry with a specific role in morphogenesis of muscle cells. In myoblasts, mediates PS enrichment at the inner leaflet of plasma membrane, triggering PIEZO1-dependent Ca2+ influx and Rho GTPases signal transduction, subsequently leading to the assembly of cortical actomyosin fibers and myotube formation (PubMed:29799007). May be involved in the uptake of farnesyltransferase inhibitor drugs, such as lonafarnib. |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF16209 |
PhoLip_ATPase_N |
26 → 97 |
Phospholipid-translocating ATPase N-terminal |
Family |
PF00122 |
E1-E2_ATPase |
124 → 377 |
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Family |
PF13246 |
Cation_ATPase |
476 → 587 |
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Family |
PF16212 |
PhoLip_ATPase_C |
851 → 1103 |
Phospholipid-translocating P-type ATPase C-terminal |
Family |
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Sequence |
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Sequence length |
1134 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Disease name |
Disease term |
References |
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Basal Cell Neoplasm |
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Basal Cell Cancer |
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Bronchiectasis |
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Basal cell carcinoma |
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Hamman-Rich Disease |
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Gastroesophageal reflux disease |
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Honeycomb lung |
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Lung Diseases, Interstitial |
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Pulmonary Fibrosis |
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Idiopathic Pulmonary Fibrosis |
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Familial Idiopathic Pulmonary Fibrosis |
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Hamman-Rich syndrome |
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