Expanding the Molecular and Clinical Phenotype of SSR4-CDG

Hum Mutat. 2015 Nov;36(11):1048-51. doi: 10.1002/humu.22856. Epub 2015 Aug 27.

Abstract

Congenital disorders of glycosylation (CDG) are a group of mostly autosomal recessive disorders primarily characterized by neurological abnormalities. Recently, we described a single CDG patient with a de novo mutation in the X-linked gene, Signal Sequence Receptor 4 (SSR4). We performed whole-exome sequencing to identify causal variants in several affected individuals who had either an undifferentiated neurological disorder or unsolved CDG of unknown etiology based on abnormal transferrin glycosylation. We now report eight affected males with either de novo (4) or inherited (4) loss of function mutations in SSR4. Western blot analysis revealed that the mutations caused a complete loss of SSR4 protein. In nearly all cases, the abnormal glycosylation of serum transferrin was only slightly above the accepted normal cutoff range.

Keywords: SSR4; carbohydrate-deficient transferrin; congenital disorders of glycosylation; signal sequence receptor 4; translocon complex.

Publication types

  • Case Reports
  • Research Support, N.I.H., Extramural

MeSH terms

  • Calcium-Binding Proteins / genetics*
  • Congenital Disorders of Glycosylation / diagnosis*
  • Congenital Disorders of Glycosylation / genetics*
  • DNA Mutational Analysis
  • Exome
  • Gene Order
  • Genes, X-Linked
  • Genetic Loci
  • Humans
  • Male
  • Membrane Glycoproteins / genetics*
  • Mutation*
  • Phenotype*
  • Receptors, Cytoplasmic and Nuclear / genetics*
  • Receptors, Peptide / genetics*

Substances

  • Calcium-Binding Proteins
  • Membrane Glycoproteins
  • Receptors, Cytoplasmic and Nuclear
  • Receptors, Peptide
  • signal sequence receptor