PRPF31 Polyclonal Antibody, 20ul 3D Culture Mutations in NME1 have been

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 enzyme starts the process of inactivating and degrading leukotriene B4

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Among its related pathways are Signaling by GPCR and p53 pathway (Pathway Interaction Database)

PRPF31 Polyclonal Antibody, 20ul 3D Culture Mutations in NME1 have beenPRPF31 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.