Symbol Name ID |
Chkb
choline kinase beta MGI:1328313 |
Darker colors indicate more annotations |
Human Phenotypes | Facial palsy |
Limb-girdle muscular dystrophy |
Generalized hypotonia |
Muscle weakness |
Gowers sign |
Myotonia |
Central core regions in muscle fibers |
Increased endomysial connective tissue |
Muscular dystrophy |
Myopathy |
Disease(s) Associated with CHKB | ||||||||||
megaconial type congenital muscular dystrophy | ||||||||||
muscular dystrophy |
Mouse Phenotypes | abnormal muscle fiber morphology |
abnormal sarcolemma morphology |
abnormal skeletal muscle fiber morphology |
centrally nucleated skeletal muscle fibers |
dystrophic muscle |
muscle degeneration |
abnormal muscle physiology |
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Availability | Mouse Genotype | |||||||
Chkbrmd/Chkbrmd |
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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