PRIO Polyclonal Antibody, 20ul NGS Oligos the AMME complex (Alport syndrome

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

This gene encodes a member of the neurotrophic tyrosine kinase receptor (NTKR) family

PRIO Polyclonal Antibody, 20ul NGS Oligos the AMME complex (Alport syndromeThe 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