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Symbol
Name
ID
Clcn7
chloride channel, voltage-sensitive 7
MGI:1347048
Phenotype annotations related to hematopoietic system
Darker colors indicate more annotations
Human Phenotypes
Petechiae
Bone marrow hypocellularity
Reticulocytosis
Anemia
Abnormal leukocyte morphology
Thrombocytopenia
Splenomegaly
Disease(s) Associated with CLCN7
autosomal dominant osteopetrosis 2
autosomal recessive osteopetrosis 4

Mouse Phenotypes
increased osteoclast cell number
microgliosis
abnormal osteoclast morphology
abnormal osteoclast physiology
Availability Mouse Genotype
Clcn7tm1.1Lex/Clcn7tm1.1Lex
Clcn7tm1Tjj/Clcn7tm1Tjj
Clcn7tm2Tjj/Clcn7tm2Tjj
Clcn7tm4.1Tjj/Clcn7tm4.1Tjj
Clcn7tm5.1Tjj/Clcn7tm5.1Tjj
Clcn7tm1.1Mawa/Clcn7+
Clcn7tm1.1Teti/Clcn7+
Clcn7tm3.1Tjj/Clcn7tm3.1Tjj
Emx1tm1.1(cre)Ito/Emx1+  (conditional)

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