FAM9C Rabbit Polyclonal Antibody, 100ul Cell Separation and Collection Allelic variations at amino acid

Allelic variations at amino acid positions 654 and 655 of isoform a (positions 624 and 625 of isoform b) have been reported| with the most common allele| Ile654/Ile655| shown here

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

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mediating its entry into cells

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

FAM9C Rabbit Polyclonal Antibody, 100ul Cell Separation and Collection Allelic variations at amino acidThis 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.