MAPPING OF THE HUMAN NMDAR2B RECEPTOR SUBUNIT GENE (GRIN2B) TO CHROMOSOME 12P12

被引:22
|
作者
MANDICH, P [1 ]
SCHITO, AM [1 ]
BELLONE, E [1 ]
ANTONACCI, R [1 ]
FINELLI, P [1 ]
ROCCHI, M [1 ]
AJMAR, F [1 ]
机构
[1] UNIV BARI,INST GENET,I-70126 BARI,ITALY
关键词
D O I
10.1006/geno.1994.1366
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The N-methyl-D-aspartate (NMDA) receptor channel is essential for synaptic transmission and synaptic plasticity underlying memory, learning, and development. Three subunits of the NMDA receptor channel, NMDAR2A, NMDAR2B, and NMDAR2C (NR2A, NR2B, and NR2C), previously identified in mouse by cDNA cloning and expression, share a high level of homology, although their patterns of expression within the brain may differ. In the present work we report the localization of the gene encoding the human NMDAR2B receptor subunit (called GRIN2B for glutamate receptor, ionotropic, N-methyl-D-aspartate 2B) to chromosome 12p12 by in situ hybridization and somatic cell hybrids. (C) 1994 Academic Press, Inc.
引用
收藏
页码:216 / 218
页数:3
相关论文
共 50 条
  • [1] Mutation analysis of the NMDAR2B (GRIN2B) gene in schizophrenia
    Ohtsuki, T
    Sakurai, K
    Dou, H
    Toru, M
    Yamakawa-Kobayashi, K
    Arinami, T
    [J]. MOLECULAR PSYCHIATRY, 2001, 6 (02) : 211 - 216
  • [2] Mutation analysis of the NMDAR2B (GRIN2B) gene in schizophrenia
    T Ohtsuki
    K Sakurai
    H Dou
    M Toru
    K Yamakawa-Kobayashi
    T Arinami
    [J]. Molecular Psychiatry, 2001, 6 : 211 - 216
  • [3] Association study between the NMDA receptor subunit 2B gene(GRIN2B) and schizophrenia
    Hori, Hiroko
    Shinkai, Takahiro
    Utsunomiya, Kensuke
    Sakata, Shinichi
    Naoe, Yui
    Fukunaka, Yuko
    Shimizu, Kazuko
    Matsumoto, Chima
    Ohmori, Osamu
    Nakamura, Jun
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2006, 141B (07) : 804 - 804
  • [4] Variation in the NMDA receptor 2B subunit gene GRIN2B is associated with differential language lateralization
    Ocklenburg, Sebastian
    Arning, Larissa
    Hahn, Constanze
    Gerding, Wanda M.
    Epplen, Joerg T.
    Guentuerkuen, Onur
    Beste, Christian
    [J]. BEHAVIOURAL BRAIN RESEARCH, 2011, 225 (01) : 284 - 289
  • [5] Habituation in prepulse inhibition is affected by a polymorphism on the NMDA receptor 2B subunit gene (GRIN2B)
    Hokyo, Akira
    Kanazawa, Tetsufumi
    Uenishi, Hiroyuki
    Tsutsumi, Atsushi
    Kawashige, Seiya
    Kikuyama, Hiroki
    Glatt, Stephen J.
    Koh, Jun
    Nishimoto, Yoshiyuki
    Matsumura, Hitoshi
    Motomura, Naoyasu
    Yoneda, Hiroshi
    [J]. PSYCHIATRIC GENETICS, 2010, 20 (05) : 191 - 198
  • [6] THE NMDA RECEPTOR SUBUNIT 2B LOCUS (NMDAR2B) MAPS TO THE DISTAL END OF MURINE CHROMOSOME-6
    MADARNAS, AR
    HENDERSON, JT
    RODER, JC
    [J]. MAMMALIAN GENOME, 1994, 5 (02) : 115 - 116
  • [7] Report on 3 patients with 12p duplication including GRIN2B
    Poirsier, Celine
    Landais, Emilie
    Bednarek, Nathalie
    Nobecourt, Jean-Marie
    Khoury, Maroun
    Schmidt, Pascal
    Morville, Patrice
    Gruson, Nadine
    Clomes, Sandrine
    Michel, Nicole
    Riot, Anita
    Manjeongean, Christelle
    Gaillard, Dominique
    Doco-Fenzy, Martine
    [J]. EUROPEAN JOURNAL OF MEDICAL GENETICS, 2014, 57 (05) : 185 - 194
  • [8] Variations in the NMDA receptor subunit 2B gene (GRIN2B) and schizophrenia:: A case-control study
    Di Maria, E
    Gulli, R
    Begni, S
    De Luca, A
    Bignotti, S
    Pasini, A
    Bellone, E
    Pizzuti, A
    Dallapiccola, B
    Novelli, G
    Ajmar, F
    Gennarelli, M
    Mandich, P
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2004, 128B (01) : 27 - 29
  • [9] NMDA receptor subunit NR2B gene (GRIN2B) is associated with schizophrenia in a case control sample
    Martucci, L
    De Luca, V
    Trakalo, J
    Kennedy, JL
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2004, 130B (01): : 85 - 85
  • [10] Association of the glutamate receptor subunit gene GRIN2B with attention-deficit/hyperactivity disorder
    Dorval, K. M.
    Wigg, K. G.
    Crosbie, J.
    Tannock, R.
    Kennedy, J. L.
    Ickowicz, A.
    Pathare, T.
    Malone, M.
    Schachar, R.
    Barr, C. L.
    [J]. GENES BRAIN AND BEHAVIOR, 2007, 6 (05) : 444 - 452