Symbol Name ID |
Hnrnpu
heterogeneous nuclear ribonucleoprotein U MGI:1858195 |
Darker colors indicate more annotations |
Human Phenotypes | Generalized hypotonia |
Disease(s) Associated with HNRNPU | |
developmental and epileptic encephalopathy 54 |
Mouse Phenotypes | abnormal myocardial fiber morphology |
decreased myocardial fiber number |
increased myocardial fiber size |
dilated cardiomyopathy |
decreased ventricle muscle contractility |
decreased cardiac muscle relaxation |
increased cardiomyocyte apoptosis |
abnormal sarcomere morphology |
abnormal I band morphology |
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Availability | Mouse Genotype | |||||||||
Hnrnputm1.1Tman/Hnrnputm1.1Tman Tg(Myh6-cre)2182Mds/0 (conditional) |
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Hnrnputm1.1Tman/Hnrnputm1.1Tman Tg(Ckmm-cre)5Khn/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 04/16/2024 MGI 6.23 |
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