abnormal hair cortex keratinization Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any defect in the formation of the fibrous elements found in the hair cortex comprising acidic (Type I ) and basic (Type II) proteins that give hair such aspects as resilience, and elasticity (Mammalian Phenotype Ontology, MP_0009801)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009801
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4 gene mutations causing the abnormal hair cortex keratinization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EGFR epidermal growth factor receptor
FOXN1 forkhead box N1
TGM3 transglutaminase 3
TMEM79 transmembrane protein 79