LPAR6, lysophosphatidic acid receptor 6, 10161

N. diseases: 47; N. variants: 10
Disease: HYPOTRICHOSIS 8 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3279470
Disease: HYPOTRICHOSIS 8
HYPOTRICHOSIS 8 		0.610 GeneticVariation disease CLINVAR In silico analysis of missense mutations in LPAR6 reveals abnormal phospholipid signaling pathway leading to hypotrichosis. 25119526 2014
CUI: C3279470
Disease: HYPOTRICHOSIS 8
HYPOTRICHOSIS 8 		0.610 Biomarker disease GENOMICS_ENGLAND Families linked to LAH3 locus were further subjected to screening of the P2RY5 gene with direct DNA sequencing. 18461368 2008
CUI: C3279470
Disease: HYPOTRICHOSIS 8
HYPOTRICHOSIS 8 		0.610 GeneticVariation disease UNIPROT Disruption of P2RY5, an orphan G protein-coupled receptor, underlies autosomal recessive woolly hair. 18297072 2008
CUI: C3279470
Disease: HYPOTRICHOSIS 8
HYPOTRICHOSIS 8 		0.610 GeneticVariation disease UNIPROT G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth. 18297070 2008
CUI: C3279470
Disease: HYPOTRICHOSIS 8
HYPOTRICHOSIS 8 		0.610 GeneticVariation disease CLINVAR Families linked to LAH3 locus were further subjected to screening of the P2RY5 gene with direct DNA sequencing. 18461368 2008
CUI: C3279470
Disease: HYPOTRICHOSIS 8
HYPOTRICHOSIS 8 		0.610 GeneticVariation disease BEFREE Families linked to LAH3 locus were further subjected to screening of the P2RY5 gene with direct DNA sequencing. 18461368 2008
CUI: C3279470
Disease: HYPOTRICHOSIS 8
HYPOTRICHOSIS 8 		0.610 CausalMutation disease CLINVAR