Symbol Name ID |
Myh3
myosin, heavy polypeptide 3, skeletal muscle, embryonic MGI:1339709 |
Darker colors indicate more annotations |
Human Phenotypes | Low posterior hairline |
Short neck |
Webbed neck |
Inguinal hernia |
Umbilical hernia |
Aplasia/Hypoplasia of the abdominal wall musculature |
Short stature |
Failure to thrive |
Intrauterine growth retardation |
Disease(s) Associated with MYH3 | |||||||||
contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A | |||||||||
contractures, pterygia, and spondylocarpotarsal fusion syndrome 1B | |||||||||
distal arthrogryposis type 2B3 |
Mouse Phenotypes | decreased body weight |
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Availability | Mouse Genotype | |
Myh3tm1.2Sajm/Myh3tm1.2Sajm |
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 03/19/2024 MGI 6.23 |
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