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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Myh4
myosin, heavy polypeptide 4, skeletal muscle
MGI:1339713
18 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Myh4arl/Myh4arl
involves: C3H/HeH * C57BL/6J
abnormal gait J:181892
abnormal skeletal muscle fiber morphology J:181892
centrally nucleated skeletal muscle fibers J:181892
hindlimb paralysis J:181892
increased variability of skeletal muscle fiber size J:181892
muscular atrophy J:181892
myositis J:181892
skeletal muscle fiber degeneration J:181892
Myh4tm1Lnwd/Myh4tm1Lnwd
involves: 129/Ola * 129P2/OlaHsd * C57BL/6
abnormal skeletal muscle fiber morphology J:78886
abnormal skeletal muscle fiber type ratio J:78886
abnormal skeletal muscle morphology J:44448
decreased body weight J:44448
decreased grip strength J:44448
decreased skeletal muscle fiber number J:78886
decreased skeletal muscle mass J:44448, J:78284, J:78886
impaired skeletal muscle contractility J:44448
increased skeletal muscle fiber size J:44448, J:78886
muscle weakness J:44448
skeletal muscle fiber atrophy J:78886

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
10/10/2017
MGI 6.10
The Jackson Laboratory