Literature DB >> 11003695

A new spontaneous mouse mutation in the Kcne1 gene.

V A Letts1, A Valenzuela, C Dunbar, Q Y Zheng, K R Johnson, W N Frankel.   

Abstract

A new mouse mutant, punk rocker (allele symbol Kcne1(pkr)), arose spontaneously on a C57BL/10J inbred strain background and is characterized by a distinctive head-tossing, circling, and ataxic phenotype. It is also profoundly and bilaterally deaf. The mutation resides in the Kcne1 gene on Chromosome (Chr) 16 and has been identified as a single base change within the coding region of the third exon. The C to T nucleotide substitution causes an arginine to be altered to a termination codon at amino acid position 67, and predictably this will result in a significantly truncated protein product. The Kcne1(pkr) mutant represents the first spontaneous mouse model for the human disorder, Jervell and Lange-Nielsen syndrome, associated with mutations in the homologous KCNE1 gene on human Chr 21.

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Year:  2000        PMID: 11003695      PMCID: PMC2862908          DOI: 10.1007/s003350010178

Source DB:  PubMed          Journal:  Mamm Genome        ISSN: 0938-8990            Impact factor:   2.957


  22 in total

1.  Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death.

Authors:  A JERVELL; F LANGE-NIELSEN
Journal:  Am Heart J       Date:  1957-07       Impact factor: 4.749

2.  Alteration of channel activities and gating by mutations of slow ISK potassium channel.

Authors:  T Takumi; K Moriyoshi; I Aramori; T Ishii; S Oiki; Y Okada; H Ohkubo; S Nakanishi
Journal:  J Biol Chem       Date:  1991-11-25       Impact factor: 5.157

3.  Pathology of the ear in the cardioauditory syndrome of Jervell and Lange-Nielsen (recessive deafness with electrocardiographic abnormalities).

Authors:  I Friedmann; G R Fraser; P Froggatt
Journal:  J Laryngol Otol       Date:  1966-05       Impact factor: 1.469

4.  Subunit composition of minK potassium channels.

Authors:  K W Wang; S A Goldstein
Journal:  Neuron       Date:  1995-06       Impact factor: 17.173

5.  The MEV mouse linkage testing stock: mapping 30 novel proviral insertions and establishment of an improved stock.

Authors:  B A Taylor; L Rowe; D A Grieco
Journal:  Genomics       Date:  1993-05       Impact factor: 5.736

6.  Deafness and imbalance associated with inactivation of the secretory Na-K-2Cl co-transporter.

Authors:  E Delpire; J Lu; R England; C Dull; T Thorne
Journal:  Nat Genet       Date:  1999-06       Impact factor: 38.330

7.  ISK, a slowly activating voltage-sensitive K+ channel. Characterization of multiple cDNAs and gene organization in the mouse.

Authors:  F Lesage; B Attali; M Lazdunski; J Barhanin
Journal:  FEBS Lett       Date:  1992-04-20       Impact factor: 4.124

8.  Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in mice.

Authors:  M J Dixon; J Gazzard; S S Chaudhry; N Sampson; B A Schulte; K P Steel
Journal:  Hum Mol Genet       Date:  1999-08       Impact factor: 6.150

9.  Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses.

Authors:  Q Y Zheng; K R Johnson; L C Erway
Journal:  Hear Res       Date:  1999-04       Impact factor: 3.208

10.  Intracisternal A-type particle elements as genetic markers: detection by repeat element viral element amplified locus-PCR.

Authors:  N Kaushik; J P Stoye
Journal:  Mamm Genome       Date:  1994-11       Impact factor: 2.957

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  12 in total

1.  Postural and locomotor control in normal and vestibularly deficient mice.

Authors:  P-P Vidal; L Degallaix; P Josset; J-P Gasc; K E Cullen
Journal:  J Physiol       Date:  2004-07-08       Impact factor: 5.182

2.  Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformatics.

Authors:  Y Qiao; C Harvard; C Tyson; X Liu; C Fawcett; P Pavlidis; J J A Holden; M E S Lewis; E Rajcan-Separovic
Journal:  Hum Genet       Date:  2010-05-29       Impact factor: 4.132

Review 3.  Supporting sensory transduction: cochlear fluid homeostasis and the endocochlear potential.

Authors:  Philine Wangemann
Journal:  J Physiol       Date:  2006-07-20       Impact factor: 5.182

4.  TBX1 is required for normal stria vascularis and semicircular canal development.

Authors:  Cong Tian; Kenneth R Johnson
Journal:  Dev Biol       Date:  2019-09-21       Impact factor: 3.582

5.  Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange-Nielsen Syndrome and Romano-Ward Syndrome.

Authors:  Rabia Faridi; Risa Tona; Alessandra Brofferio; Michael Hoa; Rafal Olszewski; Isabelle Schrauwen; Muhammad Z K Assir; Akhtar A Bandesha; Asma A Khan; Atteeq U Rehman; Carmen Brewer; Wasim Ahmed; Suzanne M Leal; Sheikh Riazuddin; Steven E Boyden; Thomas B Friedman
Journal:  Hum Mutat       Date:  2018-12-12       Impact factor: 4.878

Review 6.  Genes important for otoneurological diagnostic purposes - current status and future prospects.

Authors:  K Pawlak-Osiñska; K Linkowska; T Grzybowski
Journal:  Acta Otorhinolaryngol Ital       Date:  2018-06       Impact factor: 2.124

Review 7.  Inner ear proteomics of mouse models for deafness, a discovery strategy.

Authors:  Qing Yin Zheng; Christine R Rozanas; Isolde Thalmann; Mark R Chance; Kumar N Alagramam
Journal:  Brain Res       Date:  2006-04-05       Impact factor: 3.252

8.  Secondary structure of a KCNE cytoplasmic domain.

Authors:  Jessica M Rocheleau; Steven D Gage; William R Kobertz
Journal:  J Gen Physiol       Date:  2006-12       Impact factor: 4.086

9.  A quantitative survey of gravity receptor function in mutant mouse strains.

Authors:  Sherri M Jones; Kenneth R Johnson; Heping Yu; Lawrence C Erway; Kumar N Alagramam; Natasha Pollak; Timothy A Jones
Journal:  J Assoc Res Otolaryngol       Date:  2005-12

10.  Nkcc1 (Slc12a2) is required for the regulation of endolymph volume in the otic vesicle and swim bladder volume in the zebrafish larva.

Authors:  Leila Abbas; Tanya T Whitfield
Journal:  Development       Date:  2009-08       Impact factor: 6.868

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