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CRRD ID: 1348081
Species: Homo sapiens
CRRD Object: Gene
Symbol: MN1
Name: MN1 proto-oncogene, transcriptional regulator
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)
 IAGPRGD:86286598554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases

PMID:11094079, PMID:11559848, PMID:12569362, PMID:15870292, PMID:15890672, PMID:18948418, PMID:19344873, PMID:19386590, PMID:19919682, PMID:22436304, PMID:24075189, PMID:25549701, PMID:7731705, PMID:7731706
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.