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Symbol
Name
ID
Clcn7
chloride channel, voltage-sensitive 7
MGI:1347048
Phenotype annotations related to integument
Darker colors indicate more annotations
Human Phenotypes
Petechiae
Disease(s) Associated with CLCN7
autosomal recessive osteopetrosis 4

Mouse Phenotypes
abnormal coat/hair pigmentation
abnormal hair shaft melanin granule distribution
Availability Mouse Genotype
Clcn7tm2Tjj/Clcn7tm2Tjj

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