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RGD ID: 1307977
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Atp13a2
Name: ATPase cation transporting 13A2
Acc ID: DOID:630
Term: genetic disease
Definition: Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero.
Definition Source(s): MESH:D030342,
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
QualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
 ISORGD:13429118554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases

PMID:16964263, PMID:17485642, PMID:20683840, PMID:20853184, PMID:21060012, PMID:21665991, PMID:22198378, PMID:22388936, PMID:25149416, PMID:25197640
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.