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GENE - TERM ANNOTATION REPORT

RGD ID: 69080
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Nfix
Name: nuclear factor I X
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, http://ghr.nlm.nih.gov/
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:691618554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases

 
 ISORGD:691618554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases

PMID:20673863, PMID:24924640, PMID:25118028, PMID:26193383, PMID:26200704, PMID:28442439, PMID:28584646
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.