Symbol Name ID |
Wnk1
WNK lysine deficient protein kinase 1 MGI:2442092 |
Darker colors indicate more annotations |
Human Phenotypes | Hypotonia |
Generalized hypotonia |
Disease(s) Associated with WNK1 | ||
hereditary sensory and autonomic neuropathy type 2A |
Mouse Phenotypes | abnormal myocardial trabeculae morphology |
trabecula carnea hypoplasia |
thin myocardium |
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Availability | Mouse Genotype | |||
Wnk1Gt(OST38262)Lex/Wnk1Gt(OST38262)Lex | ||||
Wnk1tm1Clhu/Wnk1tm1Clhu Tg(Tek-cre)12Flv/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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