K1H2 Polyclonal Antibody, 50ul Cell Separation and Collection Diseases associated with OPRD1 include

Diseases associated with OPRD1 include morphine dependence and heroin dependence

This gene is a member of the prenyltransferase family and encodes a protein with geranylgeranyl diphosphate (GGPP) synthase activity

DNA pol δ and DNA pol e are multisubunit enzymes

possibly acting as a bridging factor between U5 and U4/U6 snRNPs in formation of the spliceosome

Defects in PARK7 are the cause of autosomal recessive early-onset Parkinson disease 7

K1H2 Polyclonal Antibody, 50ul Cell Separation and Collection Diseases associated with OPRD1 includeThe protein encoded by this gene is a member of the keratin gene family. As a type I hair keratin, it is an acidic protein which heterodimerizes with type II keratins to form hair and nails. The type I hair keratins are clustered in a region of chromosome 17q12 q21 and have the same direction of transcription.