Literature DB >> 16114045

A family with X-linked anophthalmia: exclusion of SOX3 as a candidate gene.

Anne Slavotinek1, Stephen S Lee, Steven P Hamilton.   

Abstract

We report on a four-generation family with X-linked anophthalmia in four affected males and show that this family has LOD scores consistent with linkage to Xq27, the third family reported to be linked to the ANOP1 locus. We sequenced the SOX3 gene at Xq27 as a candidate gene for the X-linked anophthalmia based on the high homology of this gene to SOX2, a gene previously mutated in bilateral anophthlamia. However, no amino acid sequence alterations were identified in SOX3. We have improved the definition of the phenotype in males with anophthalmia linked to the ANOP1 locus, as microcephaly, ocular colobomas, and severe renal malformations have not been described in families linked to ANOP1. (c) 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 16114045     DOI: 10.1002/ajmg.a.30872

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  4 in total

1.  Exclusion of the 750-kb genetically unstable region at Xq27 as a candidate locus for prostate malignancy in HPCX1-linked families.

Authors:  Natalay Kouprina; Nicholas C O Lee; Adam Pavlicek; Alexander Samoshkin; Jung-Hyun Kim; Hee-Sheung Lee; Sudhir Varma; William C Reinhold; John Otstot; Greg Solomon; Sean Davis; Paul S Meltzer; Johanna Schleutker; Vladimir Larionov
Journal:  Genes Chromosomes Cancer       Date:  2012-06-26       Impact factor: 5.006

2.  NAA10 polyadenylation signal variants cause syndromic microphthalmia.

Authors:  Jennifer J Johnston; Kathleen A Williamson; Christopher M Chou; Julie C Sapp; Morad Ansari; Heather M Chapman; David N Cooper; Tabib Dabir; Jeffrey N Dudley; Richard J Holt; Nicola K Ragge; Alejandro A Schäffer; Shurjo K Sen; Anne M Slavotinek; David R FitzPatrick; Thomas M Glaser; Fiona Stewart; Graeme Cm Black; Leslie G Biesecker
Journal:  J Med Genet       Date:  2019-03-06       Impact factor: 6.318

Review 3.  Confirmation of Ogden syndrome as an X-linked recessive fatal disorder due to a recurrent NAA10 variant and review of the literature.

Authors:  Laura Gogoll; Katharina Steindl; Pascal Joset; Markus Zweier; Alessandra Baumer; Christina Gerth-Kahlert; Boris Tutschek; Anita Rauch
Journal:  Am J Med Genet A       Date:  2021-06-01       Impact factor: 2.802

4.  A Japanese boy with NAA10-related syndrome and hypertrophic cardiomyopathy.

Authors:  Ayumi Shishido; Naoya Morisada; Kenta Tominaga; Hiroyasu Uemura; Akiko Haruna; Hiroaki Hanafusa; Kandai Nozu; Kazumoto Iijima
Journal:  Hum Genome Var       Date:  2020-08-17
  4 in total

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