ALKBH5 Polyclonal Antibody, 20ul Site-directed Mutagenesis Mutations in this gene have

Mutations in this gene have been associated with the autosomal dominant disorder Sorsby's fundus dystrophy

Mutations in this gene are the cause of spondylometaphyseal and metatropic dysplasia and hereditary motor and sensory neuropathy type IIC

or a heterodimer composed of one alpha and one beta chain

This encoded protein regulates cell proliferation| differentiation and growth| and can modulate expression and activation of other growth factors including interferon gamma and tumor necrosis factor alpha

ALKBH5 Polyclonal Antibody, 20ul Site-directed Mutagenesis Mutations in this gene haveBelongs to the alkB family.