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Symbol
Name
ID
Hmbs
hydroxymethylbilane synthase
MGI:96112
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Muscle weakness
Respiratory paralysis
Disease(s) Associated with HMBS
acute intermittent porphyria

Mouse Phenotypes
skeletal muscle degeneration
Availability Mouse Genotype
Hmbstm2Uam/Hmbstm3Uam

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
04/30/2024
MGI 6.23
The Jackson Laboratory