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CRRD ID: 14138019
Species: Sus scrofa
CRRD Object: Gene
Symbol: RAB9B
Name: RAB9B, member RAS oncogene family
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)
 ISSRGD:125577539068941ClinVarClinVar Annotator: match by term: Inborn genetic diseases

PMID:11093273, PMID:11761472, PMID:15627202, PMID:16130097, PMID:16778599, PMID:17568416, PMID:2479017, PMID:27179222, PMID:7541901, PMID:8520726, PMID:8780101, PMID:9418954
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.