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RGD ID: 11899928
Species: Pan paniscus
RGD Object: Gene
Symbol: COL9A3
Name: collagen type IX alpha 3 chain
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:13210499068941ClinVarClinVar Annotator: match by term: Inborn genetic diseases

PMID:10090888, PMID:10353778, PMID:10655510, PMID:10678658, PMID:11968079, PMID:1560793, PMID:15917166, PMID:17881354, PMID:21922596, PMID:21965141, PMID:23967202, PMID:24273071, PMID:25381065, PMID:8222646, PMID:8819367
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.