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Article

The wooly mutation (wly) on mouse chromosome 11 is associated with a genetic defect in Fam83g.

BMC research notes - 9 May 2013

Radden Legairre A, Child Kevin M, Adkins Elisabeth B, Spacek Damek V, Feliciano Aaron M, King Thomas R

Abstract excerpt

BACKGROUND: Mice homozygous for the spontaneous wooly mutation (abbreviated wly) are recognized as early as 3-4 weeks of age by the rough or matted appearance of their coats. Previous genetic analysis has placed wly in a 5.9 Mb interval on Chromosome 11 that contains over 200 known genes. Assignment of wly to one of these genes is needed in order to provide probes that would ultimately facilitate a complete...

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Identifiers

PMID: 23656696
DOI: 10.1186/1756-0500-6-189
PMCID: PMC3663780

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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