Linkage of loci associated with two pigment mutations on mouse chromosome 13.

doi:10.1017/s0016672300029591

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Article

Linkage of loci associated with two pigment mutations on mouse chromosome 13.

Genetical research - 1 Aug 1991

Holcombe R F, Stephenson D A, Zweidler A, Stewart R M, Chapman V M, Seidman J G

Abstract excerpt

Progeny from one intra- and two inter-specific backcrosses between divergent strains of mice were typed to map multiple markers in relation to two pigment mutations on mouse chromosome 13, beige (bg) and pearl (pe). Both recessive mutants on a C57BL/6J background were crossed separately with laboratory strain PAC (M. domesticus) and the partially inbred M. musculus stock PWK. The intra- and inter-specific F1...

Topics

Animals
Blotting, Southern
Chromosome Mapping
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 6
Chromosomes, Human, Pair 7
Crosses, Genetic
Female
Genetic Linkage
Humans
Male

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Mice

Mice, Inbred C57BL

Mutation

Pigments, Biological

Polymorphism, Restriction Fragment Length

Recombination, Genetic

Source

Open in PubMed

Identifiers

PMID: 1682216
DOI: 10.1017/s0016672300029591

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-1682216-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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Linkage of loci associated with two pigment mutations on mouse chromosome 13.PMID 1682216Read ↗

A molecular genetic linkage map of mouse chromosome 13 anchored by the beige (bg) and satin (sa) loci.Semantic proximity Read ↗

Phenotypic variations of orpk mutation and chromosomal localization of modifiers influencing kidney phenotype.Semantic proximity Read ↗

An integrated genetic map of the pearl locus of mouse chromosome 13.Semantic proximity Read ↗

Positional cloning of the Chediak-Higashi syndrome gene: genetic mapping of the beige locus on mouse chromosome 13.Semantic proximity Read ↗

Physical mapping of the beige critical region on mouse chromosome 13.Semantic proximity Read ↗

rim2 (recombination-induced mutation 2) is a new allele of pearl and a mouse model of human Hermansky-Pudlak syndrome (HPS): genetic and physical mapping.Semantic proximity Read ↗

Physical mapping of the Tec and Gabrb1 loci reveals that the Wsh mutation on mouse chromosome 5 is associated with an inversion.Semantic proximity Read ↗

A genetic locus susceptible to the overt proteinuria in BUF/Mna rat.Semantic proximity Read ↗

A linkage map of mouse chromosome 1 using an interspecific cross segregating for the gld autoimmunity mutation.Semantic proximity Read ↗

A male germ cell tumor-susceptibility-determining locus, pgct1, identified on murine chromosome 13.Semantic proximity Read ↗

Nidogen/entactin (Nid) maps to the proximal end of mouse chromosome 13 linked to beige (bg) and identifies a new region of homology between mouse and human chromosomes.Semantic proximity Read ↗

The gamma phosphorylase kinase gene, Phkg, maps to mouse chromosome 5 near Gus.Semantic proximity Read ↗

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