SCN2A wt Allele

Human SCN2A wild-type allele is located in the vicinity of 2q24.3 and is approximately 153 kb in length. This allele, which encodes sodium channel protein type 2 subunit alpha protein, plays a role in both sodium transport and membrane potential. Mutation of the gene is associated with both benign familial infantile type 3 seizures and epileptic encephalopathy early infantile type 11. (NCI Thesaurus)

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SCN2A Gene

This gene is involved in neuronal excitation.

SCN1A wt Allele

Human SCN1A wild-type allele is located in the vicinity of 2q24.3 and is approximately 84 kb in length. This allele, which encodes…

SCN1A Gene

This gene is involved in sodium transport.

Sclerotium

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Sclerotherapy

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Sclerostin

Sclerostin (213 aa, ~24 kDa) is encoded by the human SOST gene. This protein plays a role in the regulation of bone…