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

Genomics

Volumn 69, Issue 1, 2000, Pages 113-119

  Kamei, Yoshimasa ^a,b   Takeda, Yasuo ^a   Teramoto, Kiyoshi ^c   Tsutsumi, Osamu ^d,e   Taketani, Yuji ^b   Watanabe, Kazutada ^a  

^a TOKYO METROPOLITAN INSTITUTE OF GERONTOLOGY   (Japan)

^b UNIVERSITY OF TOKYO   (Japan)

^c CHUGAI PHARMACEUTICAL CO LTD   (Japan)

^d UNIVERSITY OF TOKYO HOSPITAL   (Japan)

^e JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CONTACTIN; IMMUNOGLOBULIN;

AMINO ACID SEQUENCE; AMYGDALOID NUCLEUS; ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 11Q; HUMAN; HUMAN TISSUE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN LOCALIZATION;

EID: 0034306546     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.2000.6310     Document Type: Article

References (24)

1. CALL gene is haploinsufficient in a 3p-syndrome patient
2. Peter's anomaly associated with deletion of the long arm of chromosome 11
3. Ataxia and abnormal cerebellar microorganization in mice with ablated contactin gene expression
4. Molecular cloning and in situ localization of the human contactin gene (CNTN1) on chromosome 12q11-q12
5. Interstitial deletion of the long arm of chromosome 11
6. Interstitial deletion of 11q
7. Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene
8. De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)
9. Interstitial deletion of bands 11q21 → 22.3 in a three year-old girl defined using fluorescence in situ hybridization on metaphase chromosomes
10. Developmental expression of the neural adhesion molecule F3 in the rat brain
11. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study
12. cDNA cloning and chromosomal localization of neural adhesion molecule NB-3 in human
13. The human TAX1 gene encoding the axon-associated cell adhesion molecule TAG-1/axonin-1: Genomic structure and basic promoter
14. Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot-Marie-Tooth disease type 1B
15. Expression and regulation of a gene encoding neural recognition molecule NB-3 of the contactin/F3 subgroup in mouse brain
16. Linkage results on 11q21-q22 in Eastern Quebec pedigrees densely affected by schizophrenia
17. Physical and genetic maps of the deaf-waddler region on distal mouse Chr. 6
18. Plasmacytoma-associated neuronal glycoprotein, Pang, maps to mouse chromosome 6 and human chromosome 3
19. Novel neural adhesion molecules in the Contactin/F3 subgroup of the immunoglobulin superfamily: Isolation and characterization of cDNAs from rat brain
20. Aberrant splicing of neural cell adhesion molecule L1 mRNA in a family with X-linked hydrocephalus
21. Association within a family of a balanced autosomal translocation with major mental illness
22. Deletion (11)(q14.1q21)
23. Mutations in the cell adhesion molecule L1 cause mental retardation
24. Overlapping and differential expression of BIG-2, BIG-1, TAG-1, and F3: Four members of an axon-associated cell adhesion molecule subgroup of the immunoglobulin superfamily