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Symbol
Name
ID
Smchd1
SMC hinge domain containing 1
MGI:1921605
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Facial palsy
Disease(s) Associated with SMCHD1
facioscapulohumeral muscular dystrophy 2

Mouse Phenotypes
decreased prepulse inhibition
Availability Mouse Genotype
Smchd1em1(IMPC)Tcp/Smchd1+

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
04/23/2024
MGI 6.23
The Jackson Laboratory