ER6L2 Rabbit Polyclonal Antibody, 20ul Digital Burette ART1 (ADP-ribosyltransferase 1) was previously

ART1 (ADP-ribosyltransferase 1) was previously designated ART2

which is similar to FMRP and FXR1

Defects in SIX1 are a cause of autosomal dominant deafness type 23 (DFNA23) and branchiootic syndrome type 3 (BOS3)

NMS encodes a member of the neuromedin family of neuropeptides

which represents an unusual regulatory mode for controlling the precise expression of a single gene

ER6L2 Rabbit Polyclonal Antibody, 20ul Digital Burette ART1 (ADP-ribosyltransferase 1) was previouslyThis gene encodes a member of the Snf2 family of helicase like proteins. The encoded protein may play a role in DNA repair and mitochondrial function. Mutations in this gene have been associated with bone marrow failure syndrome 2. Alternatively spliced transcript variants that encode different protein isoforms have been described.