PRPF31 Polyclonal Antibody, 20ul 3D Culture This gene and FGF3

This gene and FGF3

GO annotations related to this gene include receptor binding and GABA receptor binding

Mutations in NME1 have been identified in aggressive neuroblastomas

Defects in this gene are a cause of severe combined immunodeficiency autosomal recessive T-cell-negative/B-cell-positive/NK-cell-positive (SCIDBNK)

The nuclear-encoded DNA pol γ is the only DNA polymerase required for the replication of the mitochondrial DNA

PRPF31 Polyclonal Antibody, 20ul 3D Culture This gene and FGF3PRPF31 encodes a component of the spliceosome complex and is one of several retinitis pigmentosa causing genes. When the gene product is added to the spliceosome complex, activation occurs.