Literature DB >> 11013081

Human NB-2 of the contactin subgroup molecules: chromosomal localization of the gene (CNTN5) and distinct expression pattern from other subgroup members.

Y Kamei1, Y Takeda, K Teramoto, O Tsutsumi, Y Taketani, K Watanabe.   

Abstract

NB-2 is one of the neural recognition molecules in the contactin subgroup, which belongs to the immunoglobulin superfamily. In rat, the six molecules in this subgroup that have been reported to date are contactin, TAG-1, BIG-1, BIG-2, NB-2, and NB-3. We have isolated cDNAs encoding the two splicing isoforms of human NB-2. The long isoform of human NB-2 consists of 1100 amino acids residues that are 91% homologous to rat NB-2 at the amino acid sequence level. The short isoform lacks 74 amino acid residues between residues 19 and 93 of the long isoform. Among various regions of the adult human brain, high-level expression of NB-2 was detected in the amygdala and occipital lobe, whereas expression was low in the corpus callosum, caudate nucleus, and spinal cord. Although there were some differences, the expression pattern of NB-2 was the most similar to that of BIG-1 in the brain. Likewise, contactin and BIG-2 exhibited similar expression patterns. The expression of TAG-1 showed the least regional differences. The human NB-2 gene (CNTN5) was mapped to chromosome 11q21-q22.2 by fluorescence in situ hybridization. Our results suggest that the NB-2 gene may contribute to human neurological disorders. Copyright 2000 Academic Press.

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Year:  2000        PMID: 11013081     DOI: 10.1006/geno.2000.6310

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  11 in total

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Review 2.  Pharmacogenetic biomarkers of response in Crohn's disease.

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3.  Genetic variation and neuroimaging measures in Alzheimer disease.

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Journal:  Arch Neurol       Date:  2010-06

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Journal:  Environ Int       Date:  2011-04-05       Impact factor: 9.621

5.  The protein tyrosine phosphatases PTPRZ and PTPRG bind to distinct members of the contactin family of neural recognition molecules.

Authors:  Samuel Bouyain; Dara J Watkins
Journal:  Proc Natl Acad Sci U S A       Date:  2010-01-21       Impact factor: 11.205

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7.  Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.

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8.  Nanomechanics of Ig-like domains of human contactin (BIG-2).

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Journal:  J Mol Model       Date:  2011-03-29       Impact factor: 1.810

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Journal:  Transl Psychiatry       Date:  2021-02-04       Impact factor: 6.222

10.  Identifying relationships among genomic disease regions: predicting genes at pathogenic SNP associations and rare deletions.

Authors:  Soumya Raychaudhuri; Robert M Plenge; Elizabeth J Rossin; Aylwin C Y Ng; Shaun M Purcell; Pamela Sklar; Edward M Scolnick; Ramnik J Xavier; David Altshuler; Mark J Daly
Journal:  PLoS Genet       Date:  2009-06-26       Impact factor: 5.917

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