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Symbol
Name
ID

Kctd7
potassium channel tetramerisation domain containing 7
MGI:2442265

Phenotype annotations related to skeleton

Darker colors indicate more annotations

Human Phenotypes	Microcephaly
Disease(s) Associated with KCTD7	Microcephaly
progressive myoclonus epilepsy 3

Mouse Phenotypes		abnormal bone structure
Availability	Mouse Genotype	abnormal bone structure
	Kctd7^em2(IMPC)Bay/Kctd7^em2(IMPC)Bay

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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