Literature DB >> 8586441

Cloning and characterization of a novel zinc finger gene in Xp11.2.

J M Derry1, U Jess, U Francke.   

Abstract

During a systematic search for open reading frames in chromosome band Xp11.2, a novel gene (ZNF157) that encodes a putative 506-amino-acid protein with the sequence characteristics of a zinc-finger-containing transcription factor was isolated. ZNF157 is encoded by four exons distributed over > 20 kb of genomic DNA. The second and third exons contain sequences similar to those of the previously described KRAB-A and KRAB-B domains, motifs that have been shown to mediate transcriptional repression in other members of the protein family. A fourth exon contains 12 zinc finger DNA binding motifs and finger linking regions characteristic of ZNF proteins of the Krüppel family. ZNF157 maps to the telomeric end of a cluster of ZNF genes that includes ZNF21, ZNF41, and ZNF81.

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Year:  1995        PMID: 8586441     DOI: 10.1006/geno.1995.0031

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


  5 in total

1.  Polymorphic X-chromosome inactivation of the human TIMP1 gene.

Authors:  C L Anderson; C J Brown
Journal:  Am J Hum Genet       Date:  1999-09       Impact factor: 11.025

2.  ZNF674: a new kruppel-associated box-containing zinc-finger gene involved in nonsyndromic X-linked mental retardation.

Authors:  Dorien Lugtenberg; Helger G Yntema; Martijn J G Banning; Astrid R Oudakker; Helen V Firth; Lionel Willatt; Martine Raynaud; Tjitske Kleefstra; Jean-Pierre Fryns; Hans-Hilger Ropers; Jamel Chelly; Claude Moraine; Jozef Gecz; Jeroen van Reeuwijk; Sander B Nabuurs; Bert B A de Vries; Ben C J Hamel; Arjan P M de Brouwer; Hans van Bokhoven
Journal:  Am J Hum Genet       Date:  2005-12-29       Impact factor: 11.025

3.  Exome survey of individuals affected by VATER/VACTERL with renal phenotypes identifies phenocopies and novel candidate genes.

Authors:  Caroline M Kolvenbach; Amelie T van der Ven; Franziska Kause; Shirlee Shril; Marcello Scala; Dervla M Connaughton; Nina Mann; Makiko Nakayama; Rufeng Dai; Thomas M Kitzler; Ronen Schneider; Luca Schierbaum; Sophia Schneider; Andrea Accogli; Annalaura Torella; Gianluca Piatelli; Vincenzo Nigro; Valeria Capra; Bernd Hoppe; Stefanie Märzheuser; Eberhard Schmiedeke; Heidi L Rehm; Shrikant Mane; Richard P Lifton; Gabriel C Dworschak; Alina C Hilger; Heiko Reutter; Friedhelm Hildebrandt
Journal:  Am J Med Genet A       Date:  2021-08-02       Impact factor: 2.578

4.  A new approach to chromosome-wide analysis of X-linked markers identifies new associations in Asian and European case-parent triads of orofacial clefts.

Authors:  Øivind Skare; Håkon K Gjessing; Miriam Gjerdevik; Øystein A Haaland; Julia Romanowska; Rolv T Lie; Astanand Jugessur
Journal:  PLoS One       Date:  2017-09-06       Impact factor: 3.240

5.  Analysis of Parent-of-Origin Effects on the X Chromosome in Asian and European Orofacial Cleft Triads Identifies Associations with DMD, FGF13, EGFL6, and Additional Loci at Xp22.2.

Authors:  Øivind Skare; Rolv T Lie; Øystein A Haaland; Miriam Gjerdevik; Julia Romanowska; Håkon K Gjessing; Astanand Jugessur
Journal:  Front Genet       Date:  2018-02-22       Impact factor: 4.599

  5 in total

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