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Article

A modifying locus for familial adenomatous polyposis may be present on chromosome 1p35-p36.

Journal of medical genetics - 1 Apr 1996

Tomlinson I P, Neale K, Talbot I C, Spigelman A D, Williams C B, Phillips R K, Bodmer W F

Abstract excerpt

Mutations of the APC gene cause familial adenomatous polyposis (FAP) in humans and multiple intestinal neoplasia (Min) in laboratory mouse strains. A dominant modifying gene (Mom1), which partially suppresses the min phenotype, has been mapped to mouse chromosome 4. This region is syntenic with h...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 8730279
DOI: 10.1136/jmg.33.4.268
PMCID: PMC1050573

Genes

FAP
APC

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-8730279-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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A modifying locus for familial adenomatous polyposis may be present on chromosome 1p35-p36.PMID 8730279Read ↗

Identification of a modifier gene locus on chromosome 1p35-36 in familial adenomatous polyposis.Semantic proximity Read ↗

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The secretory phospholipase A2 gene is a candidate for the Mom1 locus, a major modifier of ApcMin-induced intestinal neoplasia.Semantic proximity Read ↗

Genetic basis of variation in adenoma multiplicity in ApcMin/+ Mom1S mice.Semantic proximity Read ↗

Genetic mapping of novel modifiers for ApcMin induced intestinal polyps’ development using the genetic architecture power of the collaborative cross miceSemantic proximity Read ↗

Genetic dissection of the Mom5 modifier locus and evaluation of Mom5 candidate genes.Semantic proximity Read ↗

Three secretory phospholipase A(2) genes that map to human chromosome 1P35-36 are not mutated in individuals with attenuated adenomatous polyposis coli.Semantic proximity Read ↗

Explaining variation in familial adenomatous polyposis: relationship between genotype and phenotype and evidence for modifier genes.Semantic proximity Read ↗

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