Identification of a modifier gene locus on chromosome 1p35-36 in familial adenomatous polyposis

Hum Genet. 1997 May;99(5):653-7. doi: 10.1007/s004390050423.


Phenotypic variability based on nonallelic heterogeneity is a characteristic feature of the dominantly inherited disease, familial adenomatous polyposis (FAP). A modifying locus, called Mom-1, which strongly influences disease expression has been mapped in the mouse model of FAP to the region of murine chromosome 4, which has synteny to human chromosome 1p35-36. In the present study, this chromosomal region was investigated by using 14 microsatellite markers within a large FAP kindred in which patients harbor the same germ-line mutation but show markedly different disease characteristics. The linkage program MLINK was used to determine whether any correlation exists between these markers and the development of extracolonic symptoms in polyposis coli patients. Depending on the mode of inheritance of the affected locus, a maximum lod score was observed for markers D1S211 and D1S197, reaching 2.08 and 1.77, respectively. The observed values obtained within one large FAP family are supportive of a phenotype-modifying locus within this chromosomal region.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenomatous Polyposis Coli / genetics*
  • Animals
  • Chromosome Mapping
  • Chromosomes, Human, Pair 1*
  • Female
  • Genes, Dominant
  • Genes, Recessive
  • Genetic Linkage
  • Genetic Markers
  • Humans
  • Lod Score
  • Male
  • Mice
  • Microsatellite Repeats
  • Pedigree
  • Phenotype
  • Software


  • Genetic Markers