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Symbol
Name
ID
Myh3
myosin, heavy polypeptide 3, skeletal muscle, embryonic
MGI:1339709
Phenotype annotations related to growth/size/body
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
Availability Mouse Genotype
Myh3tm1.2Sajm/Myh3tm1.2Sajm

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
03/19/2024
MGI 6.23
The Jackson Laboratory