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CRRD ID: 11998560
Species: Pan paniscus
CRRD Object: Gene
Symbol: RALGAPA1
Name: Ral GTPase activating protein catalytic alpha subunit 1
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.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
RALGAPA1 ISSRGD:7316359068941ClinVarClinVar Annotator: match by term: Inborn genetic diseases

PMID:11477612, PMID:15498464, PMID:19520869, PMID:19733229, PMID:21148297, PMID:21744488, PMID:23136410, PMID:24389102, PMID:24672426, PMID:24857653, PMID:25799227, PMID:26542245, PMID:27323939, PMID:27340022
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.