Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55806
Gene Symbol: HR
HR
0.430 GeneticVariation disease BEFREE Marie Unna Hereditary Hypotrichosis 1 (MUHH1; OMIM 146550), a rare monogenic condition characterized by the development of sparse, twisted hair or complete hair loss, is the consequence of mutations located in the hairless (HR) gene. 22584530 2012
Entrez Id: 55806
Gene Symbol: HR
HR
0.430 AlteredExpression disease BEFREE Our results establish the link between MUHH and U2HR, show that fine-tuning of HR protein levels is important in control of hair growth, and identify a potential mechanism for preventing hair loss or promoting hair removal. 19122663 2009
Entrez Id: 55806
Gene Symbol: HR
HR
0.430 Biomarker disease CTD_human A novel missense mutation in the mouse hairless gene causes irreversible hair loss: genetic and molecular analyses of Hr m1Enu. 16455232 2006
Entrez Id: 55806
Gene Symbol: HR
HR
0.430 GeneticVariation disease LHGDN The hairless gene in androgenetic alopecia: results of a systematic mutation screening and a family-based association approach. 11966690 2002
Entrez Id: 55806
Gene Symbol: HR
HR
0.430 Biomarker disease HPO