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GENE - TERM ANNOTATION REPORT

RGD ID: 1308669
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Foxp1
Name: forkhead box P1
Acc ID: DOID:0070338
Term: cerebellar hypoplasia
Definition: A cerebellar disease that is characterized by a cerebellum that is smaller than usual or not completely developed. (DO)
Definition Source(s): https://en.wikipedia.org/wiki/Cerebellar_hypoplasia "DO" "DO", https://www.ninds.nih.gov/health-information/disorders/cerebellar-hypoplasia "DO" "DO"
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.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
Foxp1 ISOFOXP1 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Congenital cerebellar hypoplasiaPMID:25741868 PMID:28492532 PMID:31474318
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