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Symbol
Name
ID
Mylk
myosin, light polypeptide kinase
MGI:894806
Phenotype annotations related to mortality/aging
Darker colors indicate more annotations
Human Phenotypes
Death in infancy
Sudden cardiac death
Sudden death
Disease(s) Associated with MYLK
coronary artery disease
megacystis-microcolon-intestinal hypoperistalsis syndrome
thoracic aortic aneurysm

Mouse Phenotypes
premature death
neonatal lethality, incomplete penetrance
prenatal lethality, incomplete penetrance
Availability Mouse Genotype
Mylktm1.1Bph/Mylktm1.1Bph
Tg(Myh11-cre,-EGFP)2Mik/0  (conditional)
Mylktm1Mzhu/Mylktm1Mzhu
Taglntm1(cre/ERT2)Feil/?  (conditional)
Mylktm1.1Bph/Mylktm1.2Bph
Tg(Myh11-cre,-EGFP)2Mik/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