Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10161
Gene Symbol: LPAR6
LPAR6 		0.610 GeneticVariation disease CLINVAR In silico analysis of missense mutations in LPAR6 reveals abnormal phospholipid signaling pathway leading to hypotrichosis. 25119526 2014
Entrez Id: 10161
Gene Symbol: LPAR6
LPAR6 		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
Entrez Id: 10161
Gene Symbol: LPAR6
LPAR6 		0.610 GeneticVariation disease UNIPROT Disruption of P2RY5, an orphan G protein-coupled receptor, underlies autosomal recessive woolly hair. 18297072 2008
Entrez Id: 10161
Gene Symbol: LPAR6
LPAR6 		0.610 GeneticVariation disease UNIPROT G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth. 18297070 2008
Entrez Id: 10161
Gene Symbol: LPAR6
LPAR6 		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
Entrez Id: 10161
Gene Symbol: LPAR6
LPAR6 		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
Entrez Id: 10161
Gene Symbol: LPAR6
LPAR6 		0.610 CausalMutation disease CLINVAR
Entrez Id: 147183
Gene Symbol: KRT25
KRT25 		0.100 CausalMutation disease CLINVAR A homozygous missense variant in type I keratin KRT25 causes autosomal recessive woolly hair. 26160856 2015
Entrez Id: 5925
Gene Symbol: RB1
RB1 		0.100 GeneticVariation disease CLINVAR In silico analysis of missense mutations in LPAR6 reveals abnormal phospholipid signaling pathway leading to hypotrichosis. 25119526 2014
Entrez Id: 5925
Gene Symbol: RB1
RB1 		0.100 GeneticVariation disease CLINVAR Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3). 18461368 2008
Entrez Id: 5925
Gene Symbol: RB1
RB1 		0.100 CausalMutation disease CLINVAR
Entrez Id: 148
Gene Symbol: ADRA1A
ADRA1A 		0.010 GeneticVariation disease BEFREE Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3). 18461368 2008
Entrez Id: 57007
Gene Symbol: ACKR3
ACKR3 		0.010 GeneticVariation disease BEFREE Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3). 18461368 2008
Entrez Id: 6754
Gene Symbol: SSTR4
SSTR4 		0.010 GeneticVariation disease BEFREE Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3). 18461368 2008
Entrez Id: 680
Gene Symbol: BRS3
BRS3 		0.010 GeneticVariation disease BEFREE Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3). 18461368 2008
Entrez Id: 200879
Gene Symbol: LIPH
LIPH 		0.010 GeneticVariation disease BEFREE Genotyping using microsatellite markers linked to three autosomal recessive forms of hypotrichosis (LAH1, LAH2, LAH3) showed the linkage of 2 families to the LAH2 locus and 14 to the LAH3 locus. 18461368 2008
Entrez Id: 2866
Gene Symbol: GPR42
GPR42 		0.010 GeneticVariation disease BEFREE Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3). 18461368 2008
Entrez Id: 10663
Gene Symbol: CXCR6
CXCR6 		0.010 GeneticVariation disease BEFREE Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3). 18461368 2008
Entrez Id: 9170
Gene Symbol: LPAR2
LPAR2 		0.010 GeneticVariation disease BEFREE Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3). 18461368 2008
Entrez Id: 151
Gene Symbol: ADRA2B
ADRA2B 		0.010 GeneticVariation disease BEFREE Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3). 18461368 2008
Entrez Id: 1909
Gene Symbol: EDNRA
EDNRA 		0.010 GeneticVariation disease BEFREE Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3). 18461368 2008