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Symbol
Name
ID
Hnrnpu
heterogeneous nuclear ribonucleoprotein U
MGI:1858195
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Generalized hypotonia
Disease(s) Associated with HNRNPU
early infantile epileptic encephalopathy 54

Mouse Phenotypes
abnormal myocardial fiber morphology
decreased myocardial fiber number
enlarged myocardial fiber
dilated cardiomyopathy
decreased ventricle muscle contractility
decreased cardiac muscle relaxation
increased cardiomyocyte apoptosis
abnormal sarcomere morphology
abnormal I band morphology
Availability Mouse Genotype
Hnrnputm1.1Tman/Hnrnputm1.1Tman
Tg(Myh6-cre)2182Mds/0  (conditional)
Hnrnputm1.1Tman/Hnrnputm1.1Tman
Tg(Ckmm-cre)5Khn/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
10/08/2019
MGI 6.14
The Jackson Laboratory