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GP162 Polyclonal Antibody, 50ul Cell Labeling & Imaging Mutations in this gene have

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GP162 Polyclonal Antibody, 50ul Cell Labeling & Imaging Mutations in this gene haveThis gene was identified upon genomic analysis of a gene dense region at human chromosome 12p13. It appears to be mainly expressed in the brain; however, its function is not known. Alternatively spliced transcript variants encoding different isoforms have been identified.

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Description

Mutations in this gene have been associated with hemolytic anemia due to hexokinase deficiency

This keratin has been coexpressed with keratin 14 in a number of epithelial tissues

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It is associated with packaging

Some of these associations were further supported by gene expression analyses and an association study in essential hypersomnia (EHS)

GP162 Polyclonal Antibody, 50ul Cell Labeling & Imaging Mutations in this gene haveThis gene was identified upon genomic analysis of a gene dense region at human chromosome 12p13. It appears to be mainly expressed in the brain; however, its function is not known. Alternatively spliced transcript variants encoding different isoforms have been identified.

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