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Article

Patchy fur, a mouse coat mutation associated with X-Y nondisjunction, maps to the pseudoautosomal boundary region.

Genomics - 15 Dec 1998

Korobova O, Lane P W, Perry J, Palmer S, Ashworth A, Davisson M T, Arnheim N

Abstract excerpt

Patchy fur is a semidominant X-linked mutation in the mouse, resulting in a sparse coat. The Paf mutation also alters the normal segregation of the X and the Y chromosomes during male meiosis by causing nondisjunction at anaphase I. Analysis of 1139 female meioses from an intersubspecific backcross using 15 PCR-based markers localizes Paf to an approximately 0.2-cM interval that includes the pseudoautosomal...

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Source

Identifiers

PMID: 9878259
DOI: 10.1006/geno.1998.5528

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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Patchy fur, a mouse coat mutation associated with X-Y nondisjunction, maps to the pseudoautosomal boundary region.PMID 9878259Read ↗

Patchy fur (Paf), a semidominant X-linked gene associated with a high level of X-Y nondisjunction in male mice.Semantic proximity Read ↗

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A high frequency of XO offspring from X(Paf)Y* male mice: evidence that the Paf mutation involves an inversion spanning the X PAR boundary.Semantic proximity Read ↗

A pronounced evolutionary shift of the pseudoautosomal region boundary in house mice.Semantic proximity Read ↗

High frequency de novo alterations in the long-range genomic structure of the mouse pseudoautosomal region.Semantic proximity Read ↗

The amelogenin loci span an ancient pseudoautosomal boundary in diverse mammalian speciesSemantic proximity Read ↗

Instability of the pseudoautosomal boundary in house miceSemantic proximity Read ↗

Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X chromosome: implications for mapping human disorders in Xq28.Semantic proximity Read ↗

Mapping of PCR-based markers for mouse chromosome 4 on a backcross penetrant for the misty (m) mutation.Semantic proximity Read ↗

Faint lined (Fnl): a novel X-linked coat mutant in the mouse.Semantic proximity Read ↗

The proper interplay between the expression of Spo11 splice isoforms and the structure of the pseudoautosomal region promotes XY chromosomes recombination.Semantic proximity Read ↗

Physical and genetic characterization reveals a pseudogene, an evolutionary junction, and unstable loci in distal Xq28.Semantic proximity Read ↗

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