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RGD ID: 1565592
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Aff2
Name: AF4/FMR2 family, member 2
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:13432368554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases

 ISORGD:13432368554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases

PMID:10424820, PMID:10651894, PMID:10780779, PMID:10964075, PMID:11246464, PMID:16118346, PMID:20655035, PMID:21330300, PMID:21739600, PMID:22773736, PMID:23849776, PMID:8651263, PMID:9341861
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.