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RGD ID: 2623
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Fmr1
Name: fragile X mental retardation 1
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:7359198554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases

PMID:10448821, PMID:10611212, PMID:12418611, PMID:12529854, PMID:12871874, PMID:15052536, PMID:16700053, PMID:17166801, PMID:19367323, PMID:20799337, PMID:22463693, PMID:24448548, PMID:25171808, PMID:29178241, PMID:8037202, PMID:8490650, PMID:9606468
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.