Symbol Name ID |
Insr
insulin receptor MGI:96575 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Hypertrophic cardiomyopathy |
Disease(s) Associated with INSR | |
Donohue syndrome |
Mouse Phenotypes | cardiovascular system phenotype |
abnormal retina vasculature morphology |
abnormal retina blood vessel morphology |
abnormal retina blood vessel pattern |
abnormal vascular plexus formation |
increased cardiac muscle glycogen level |
decreased myocardial fiber size |
abnormal heart development |
small heart |
decreased heart left ventricle weight |
decreased heart left ventricle posterior wall thickness |
abnormal cardiovascular system physiology |
decreased coronary flow rate |
decreased cardiac output |
abnormal cardiac muscle cell glucose uptake |
decreased cardiac muscle cell glucose uptake |
increased cardiac muscle cell glucose uptake |
decreased cardiac muscle contractility |
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Availability | Mouse Genotype | ||||||||||||||||||
Insrtm1Khn/Insrtm1Khn Tg(Ckmm-cre)5Khn/0 (conditional) |
* | ||||||||||||||||||
Insrtm1Khn/Insrtm1Khn Tg(Myhca-cre)1Abel/0 (conditional) |
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Insrtm1Khn/Insrtm1Khn Tg(Pdgfrb-cre)#Rha/0 (conditional) |
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 04/23/2024 MGI 6.23 |
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