RBM10 Polyclonal Antibody, 50ul Metabolic enzymes The encoded protein is associated

The encoded protein is associated with several phenotypes- Greig cephalopolysyndactyly syndrome

Mutations in this gene have been associated with Niemann-Pick disease| type C2 and frontal lobe atrophy

and house dust mite

This gene belongs to the solute carrier 2A family

Required for interleukin-2 (IL2) production

RBM10 Polyclonal Antibody, 50ul Metabolic enzymes The encoded protein is associatedThis gene encodes a nuclear protein that belongs to a family proteins that contain an RNA binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.