FAM9C Rabbit Polyclonal Antibody, 100ul Cell Separation and Collection Mutations in CYP7B1 have been

Mutations in CYP7B1 have been associated with hereditary spastic paraplegia (SPG5 or HSP)

Catalytic activity:ATP + a [protein]-L-tyrosine = ADP + a [protein]-L-tyrosine phosphate

mediating its entry into cells

Gene Ontology (GO) annotations related to this gene include acetylglucosaminyltransferase activity

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FAM9C Rabbit Polyclonal Antibody, 100ul Cell Separation and Collection Mutations in CYP7B1 have beenThis gene is a member of a gene family which arose through duplication on the X chromosome. The encoded protein may be localized to the nucleus as the protein contains several nuclear localization signals and has similarity to a synaptonemal complex protein.