H17B6 Rabbit Polyclonal Antibody, 50ul Sampling Tubes Mutations in this gene are

Mutations in this gene are a cause of autosomal recessive spinocerebellar ataxia-11 (SCAR11)

This gene encodes a member of von Willebrand factor A domain containing protein family

This protein noncovalently binds to an alpha subunit to form a heterodimeric integrin complex

This gene encodes an oxidative stress response protein that regulates cell death

such as diabetes

H17B6 Rabbit Polyclonal Antibody, 50ul Sampling Tubes Mutations in this gene areThe protein encoded by this gene has both oxidoreductase and epimerase activities and is involved in androgen catabolism. The oxidoreductase activity can convert 3 alpha adiol to dihydrotestosterone while the epimerase activity can convert androsterone to epi androsterone. Both reactions use NAD+ as the preferred cofactor. This gene is a member of the retinol dehydrogenase family.