Details for phenotype: autosomal recessive woolly hair

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EndoNet ID: ENP00288

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Name

autosomal recessive woolly hair

General information

This phenotype is pathologic

Links to other resources

GO	negative regulation of anagen
OMIM	278150
Medline Plus	003246
MeSH term	67536745

Phenotype triggers

• no activity (knock out experiment or RNAi) of Lysophosphatidic acid receptor 6 ui-button
  in hair_follicle ui-button
  • P2Y5 was identified as a critical mediator for human hair growth and is a causal gene of a rare familial form of human hair loss. [1]

EndoNet at the Institut for Bioinformatics UMG Göttingen