Atypical ZFHX1B mutation associated with a mild Mowat-Wilson syndrome phenotype

Am J Med Genet A. 2006 Apr 15;140(8):869-72. doi: 10.1002/ajmg.a.31196.

Abstract

Mowat-Wilson syndrome is a recently delineated severe mental retardation, multiple congenital anomalies syndrome caused by dominant nonsense or frameshift mutations, deletions or translocations of the zinc finger homeobox 1B gene (ZFHX1B). We report on a patient with exceptional mild phenotype caused by a novel and unusual splice mutation in the 5'UTR. The aberrant transcript leads to usage of an alternative upstream start codon. The resulting protein differs from the wild-type only in the first 24 amino acids. The aberrant protein therefore contains all known functional domains, but might lack a so far unrecognized putative N-terminal acylation site, which is probably important for neuronal function and facial structures.

Publication types

  • Case Reports
  • Review

MeSH terms

  • 5' Untranslated Regions*
  • Abnormalities, Multiple / genetics*
  • Acylation
  • Amino Acid Sequence
  • Child, Preschool
  • Homeodomain Proteins / genetics*
  • Humans
  • Infant
  • Infant, Newborn
  • Intellectual Disability / genetics*
  • Male
  • Molecular Sequence Data
  • Mutation*
  • Phenotype
  • RNA Splice Sites / genetics
  • Repressor Proteins / genetics*
  • Syndrome
  • Zinc Finger E-box Binding Homeobox 2

Substances

  • 5' Untranslated Regions
  • Homeodomain Proteins
  • RNA Splice Sites
  • Repressor Proteins
  • ZEB2 protein, human
  • Zinc Finger E-box Binding Homeobox 2