PRIO Polyclonal Antibody, 20ul NGS Oligos fusing this gene and the

fusing this gene and the fibroblast growth factor receptor 1 (FGFR1) gene

This gene encodes a 59 kDa protein that is associated with the U11 small nuclear ribonucleoprotein (snRNP)

the AMME complex (Alport syndrome

Mutations in this gene are associated with autosomal recessive nonsyndromic deafness (DFNB82)

Methylation of the CpG island leads to transcriptional silencing of this gene

PRIO Polyclonal Antibody, 20ul NGS Oligos fusing this gene and theThe protein encoded by this gene is a membrane glycosylphosphatidylinositol anchored glycoprotein that tends to aggregate into rod like structures. The encoded protein contains a highly unstable region of five tandem octapeptide repeats. This gene is found on chromosome 20, approximately 20 kbp upstream of a gene which encodes a biochemically and structurally similar protein to the one encoded by this gene. Mutations in the repeat region as well as