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Symbol
Name
ID
Pex13
peroxisomal biogenesis factor 13
MGI:1919379
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Infantile muscular hypotonia
Severe muscular hypotonia
Disease(s) Associated with PEX13
peroxisome biogenesis disorder 11A

Mouse Phenotypes
hypotonia
Availability Mouse Genotype
Pex13tm1.1Crne/Pex13tm1.1Crne

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
11/12/2019
MGI 6.14
The Jackson Laboratory