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GENE - TERM ANNOTATION REPORT

RGD ID: 2915
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Ins1
Name: insulin 1
Acc ID: DOID:9004035
Term: Segawa Syndrome, Autosomal Recessive
Definition: null
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)
Ins1 ISOINS-IGF2 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Autosomal recessive DOPA responsive dystoniaPMID:11921414 PMID:12610512 PMID:18162506 PMID:18171712 PMID:20809526 PMID:22264700 PMID:24753243 PMID:25542748 PMID:25741868 PMID:26101329 PMID:26467025 PMID:27635400 PMID:28492532 PMID:30456822 PMID:33206859 PMID:33953728
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