Genetic Analysis of von Hippel-Lindau Disease

M Nordstrom-O'Brien, RB van der Luijt, E van Rooijen, Ans van den Ouweland, Danielle Majoor - Krakauer, MP Lolkema, A van Brussel, EE Voest, RH Giles

Research output: Contribution to journalArticleAcademicpeer-review

232 Citations (Scopus)

Abstract

Mutations in the von Hippel-Lindau (VHL) gene are responsible for VHL disease, congenital polycythemia, and are found in many sporadic tumor types as well. Reports of VHL mutations are dispersed throughout original articles and databases that have not been recently updated. We compiled a comprehensive mutation table of 1,548 germline and somatic VHL mutations, derived from this protein of only 213 amino acids. We describe detailed phenotype and gene mutation information for 945 VHL families, including 30 previously unpublished kindreds from The Netherlands (six novel mutations). These data represent the most extensive catalog of germline VHL mutations to date. We also review VHL disease, known and theorized pathogenesis of common VHL manifestations, and genotype phenotype correlations. Analysis of all VHL families, excluding germline mutations resulting in congenital polycythemias, describes the spectrum of mutation types: 52% missense, 13% frameshift, 11% nonsense, 6% in-frame deletions/insertions, 11% large/complete deletions, and 7% splice mutations. This easy-to-use compilation of VHL mutations is intended to facilitate research and function as a necessary adjunct for physicians when providing patient information. Hum Mutat 31:521-537, 2010. (C) 2010 Wiley-Liss, Inc.
Original languageUndefined/Unknown
Pages (from-to)521-537
Number of pages17
JournalHuman Mutation
Volume31
Issue number5
DOIs
Publication statusPublished - 2010

Research programs

  • EMC COEUR-09
  • EMC MGC-02-96-01

Cite this