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Symbol
Name
ID
Insr
insulin receptor
MGI:96575
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Fatigue
Disease(s) Associated with INSR
familial hyperinsulinemic hypoglycemia 5

Mouse Phenotypes
polydipsia
abnormal circadian feeding behavior
polyphagia
Availability Mouse Genotype
Insrtm1Khn/Insrtm1Khn
Tg(Nes-cre)1Kln/0  (conditional)
Insrtm1Khn/Insrtm1Khn
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
Tg(Ins2-cre)25Mgn/0  (conditional)
Insrtm1Khn/Insrtm1Khn
Tg(Slc2a4-cre)546Dac/0  (conditional)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory