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The mouse wellhaarig (we) mutations result from defects in epidermal-type transglutaminase 3 (Tgm3).

Molecular genetics and metabolism - 1 Nov 2015

Brennan Brett M, Huynh Minh T, Rabah Mohammed A, Shaw Hailie E, Bisaillon Jason J, Radden Legairre A, Nguyen Tu V, King Thomas R

Abstract excerpt

The recessive wellhaarig (we) mutations, named for the wavy coat and curly whiskers they generate in homozygotes, have previously been mapped on mouse Chromosome 2. To further limit the possible location of the we locus, we crossed hybrid (C57BL/6×AKR)F1, we(4J)/+ females with AKR, we(4J)/we(4J) mutant males to create a large backcross family that was typed for various microsatellite markers and single-nucleotide...

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Identifiers

PMID: 26194162
DOI: 10.1016/j.ymgme.2015.07.002
PMCID: PMC4640993

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

Source receipt: pubmed, retrieved 7 Sept 2026.

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