CLCN7 wt Allele

Human CLCN7 wild-type allele is located in the vicinity of 16p13 and is approximately 31 kb in length. This allele, which encodes H(+)/Cl(-) exchange transporter 7 protein, is involved in chloride ion transport. Mutation of the gene is associated with both osteopetrosis autosomal dominant type 2 and osteopetrosis autosomal recessive type 4. (NCI Thesaurus)

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CLCN7 Gene

This gene plays a role in ion transport.

CLCN6 wt Allele

Human CLCN6 wild-type allele is located in the vicinity of 1p36 and is approximately 37 kb in length. This allele, which encodes…

CLCN6 Gene

This gene plays a role in chloride ion transport.

CLCF1 wt Allele

Human CLCF1 wild-type allele is located in the vicinity of 11q13.3 and is approximately 10 kb in length. This allele, which encodes…

CLCF1 Gene

This gene is involved in cytokine signaling.

CLCA2 wt Allele

Human CLCA2 wild-type allele is located within1p31-p22 and is approximately 32 kb in length. This allele, which encodes chloride channel protein, may…