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CRRD ID: 733705
Species: Homo sapiens
CRRD Object: Gene
Symbol: CTNNB1
Name: catenin beta 1
Acc ID: DOID:9007653
Term: Multiple Abnormalities
Definition: Congenital abnormalities that affect more than one organ or body structure.
Definition Source(s): MESH:D000015
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)
 EXP 11554173CTDCTD Direct Evidence: marker/mechanism

 IAGPRGD:104014938554872ClinVarClinVar Annotator: match by term: Multiple congenital anomalies

PMID:11719191, PMID:15713948, PMID:15866163, PMID:15866164, PMID:18334222, PMID:1999432, PMID:21903672, PMID:22110128, PMID:22495309, PMID:22682243, PMID:23033978, PMID:23499309, PMID:24431282, PMID:24614104, PMID:24668549, PMID:25326669, PMID:25533962, PMID:27915094, PMID:28575650, PMID:8227220, PMID:8582267, PMID:9060476
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.