Literature DB >> 8449507

Localization of a highly conserved human potassium channel gene (NGK2-KV4; KCNC1) to chromosome 11p15.

T Ried1, B Rudy, E Vega-Saenz de Miera, D Lau, D C Ward, K Sen.   

Abstract

Several genes (the Shaker or Sh gene family) encoding components of voltage-gated K+ channels have been identified in various species. Based on sequence similarities Sh genes are classified into four groups or subfamilies. Mammalian genes of each one of these subfamilies also show high levels of sequence similarity to one of four related Drosophila genes: Shaker, Shab, Shaw, and Shal. Here we report the isolation of human cDNAs for a Shaw-related product (NGK2, KV3.1a) previously identified in rat and mice. A comparison of the nucleotide and deduced amino acid sequence of NGK2 in rodents and humans shows that this product is highly conserved in mammals; the human NGK2 protein shows over 99% amino acid sequence identity to its rodent homologue. The gene (NGK2-KV4; KCNC1) encoding NGK2 was mapped to human chromosome 11p15 by fluorescence in situ hybridization with the human NGK2 cDNAs.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8449507     DOI: 10.1006/geno.1993.1075

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


  7 in total

1.  Molecular evidence for a role of Shaw (Kv3) potassium channel subunits in potassium currents of dog atrium.

Authors:  L Yue; Z Wang; H Rindt; S Nattel
Journal:  J Physiol       Date:  2000-09-15       Impact factor: 5.182

2.  A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy.

Authors:  Mikko Muona; Samuel F Berkovic; Leanne M Dibbens; Karen L Oliver; Snezana Maljevic; Marta A Bayly; Tarja Joensuu; Laura Canafoglia; Silvana Franceschetti; Roberto Michelucci; Salla Markkinen; Sarah E Heron; Michael S Hildebrand; Eva Andermann; Frederick Andermann; Antonio Gambardella; Paolo Tinuper; Laura Licchetta; Ingrid E Scheffer; Chiara Criscuolo; Alessandro Filla; Edoardo Ferlazzo; Jamil Ahmad; Adeel Ahmad; Betul Baykan; Edith Said; Meral Topcu; Patrizia Riguzzi; Mary D King; Cigdem Ozkara; Danielle M Andrade; Bernt A Engelsen; Arielle Crespel; Matthias Lindenau; Ebba Lohmann; Veronica Saletti; João Massano; Michael Privitera; Alberto J Espay; Birgit Kauffmann; Michael Duchowny; Rikke S Møller; Rachel Straussberg; Zaid Afawi; Bruria Ben-Zeev; Kaitlin E Samocha; Mark J Daly; Steven Petrou; Holger Lerche; Aarno Palotie; Anna-Elina Lehesjoki
Journal:  Nat Genet       Date:  2014-11-17       Impact factor: 38.330

Review 3.  The best evidence for progressive myoclonic epilepsy: A pathway to precision therapy.

Authors:  Alessandro Orsini; Angelo Valetto; Veronica Bertini; Mariagrazia Esposito; Niccolò Carli; Berge A Minassian; Alice Bonuccelli; Diego Peroni; Roberto Michelucci; Pasquale Striano
Journal:  Seizure       Date:  2019-08-23       Impact factor: 3.184

4.  Localization of Romano-Ward long QT syndrome gene, LQT1, to the interval between tyrosine hydroxylase (TH) and D11S1349.

Authors:  M W Russell; M Dick; R M Campbell; J E Hulse; D J Munroe; E Bric; D E Housman; F S Collins; L C Brody
Journal:  Am J Hum Genet       Date:  1995-08       Impact factor: 11.025

5.  Multicolor fluorescence in situ hybridization on metaphase chromosomes and interphase Halo-preparations using cosmid and YAC clones for the simultaneous high resolution mapping of deletions in the dystrophin gene.

Authors:  C Tocharoentanaphol; M Cremer; E Schröck; L Blonden; K Kilian; T Cremer; T Ried
Journal:  Hum Genet       Date:  1994-03       Impact factor: 4.132

6.  Localization of Shaw-related K+ channel genes on mouse and human chromosomes.

Authors:  M Haas; D C Ward; J Lee; A D Roses; V Clarke; P D'Eustachio; D Lau; E Vega-Saenz de Miera; B Rudy
Journal:  Mamm Genome       Date:  1993-12       Impact factor: 2.957

7.  Isolation and chromosomal localization of a human ATP-regulated potassium channel.

Authors:  S N Krishnan; T Desai; D C Ward; G G Haddad
Journal:  Hum Genet       Date:  1995-08       Impact factor: 4.132

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.