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RGD ID: 1550411
Species: Mus musculus
RGD Object: Gene
Symbol: Arv1
Name: ARV1 homolog, fatty acid homeostasis modulator
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:13491988554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases

PMID:11063737, PMID:12145310, PMID:18287539, PMID:19883648, PMID:20663892, PMID:21539707, PMID:22265715, PMID:25558065, PMID:25741868, PMID:26460143, PMID:26479315, PMID:27270415
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.