Contactin Associated Protein Like Protein 3B (CNTNAP3B)

[Edit]

Cell recognition molecule Caspr3b

Contactin Associated Protein Like Protein 3B (CNTNAP3B)
CNTNAP3B is the result of a pericentromeric duplication of the genomic region encoding CNTNAP3 on chromosome 9. This observation suggests possible involvement of CNTNAP3 in the etiology of bladder exstrophy. Additionally, FISH analysis identified several genomic copies of CNTNAP3 on both sides of the chromosome 9 centromere flanking the polymorphic heterochromatin. Northern blot analysis of lymphoblast and bladder RNA confirmed CNTNAP3 transcripts in these tissues and did not show abnormal CNTNAP3 expression in the proband and two unrelated patients with bladder exstrophy. The identification of multiple copies of three BAC clones in the proband, his parents, and unrelated controls suggests that duplications of CNTNAP3 and the surrounding genomic region have occurred as a result of repeated events of unequal crossing over and pericentric inversions during chromosome 9 evolution.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Contactin Associated Protein Like Protein 3B (CNTNAP3B) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Contactin Associated Protein Like Protein 3B (CNTNAP3B) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Contactin Associated Protein Like Protein 3B (CNTNAP3B) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Contactin Associated Protein Like Protein 3B (CNTNAP3B) CLIA Kit Customized Service Offer
n/a ELISA Kit for Contactin Associated Protein Like Protein 3B (CNTNAP3B) ELISA Kit Customized Service Offer
  1. "Complete sequencing and characterization of 21,243 full-length human cDNAs." Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
  2. "DNA sequence and analysis of human chromosome 9." Nature 429:369-374(2004) [PubMed] [Europe PMC] [Abstract]
  3. "A reciprocal translocation 46,XY,t(8;9)(p11.2;q13) in a bladder exstrophy patient disrupts CNTNAP3 and presents evidence of a pericentromeric duplication on chromosome 9."Genomics 85:622-629(2005) [PubMed] [Europe PMC] [Abstract]