×
Entrez Id:
200879
Gene Symbol:
LIPH
LIPH
0.500
GeneticVariation
disease
BEFREE
Mutations in LPAR6/P2RY5 and LIPH are associated with woolly hair and/or hypotrichosis .
22385360
2013
×
Entrez Id:
200879
Gene Symbol:
LIPH
LIPH
0.500
GeneticVariation
disease
BEFREE
Founder mutations in the lipase h gene in families with autosomal recessive woolly hair/hypotrichosis .
19262606
2009
×
Entrez Id:
200879
Gene Symbol:
LIPH
LIPH
0.500
GeneticVariation
disease
BEFREE
In addition, the present findings suggest that the mutation patterns of LIPH might be associated with hypotrichosis severity in ARWH.
24586639
2014
×
Entrez Id:
10161
Gene Symbol:
LPAR6
LPAR6
0.500
GeneticVariation
disease
BEFREE
Autosomal recessive wooly hair/hypotrichosis phenotypes are mostly associated with pathogenic sequence variants in LIPH and LPAR6 genes.
31077348
2019
×
Entrez Id:
10161
Gene Symbol:
LPAR6
LPAR6
0.500
GeneticVariation
disease
LHGDN
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
0.500
GeneticVariation
disease
LHGDN
These results show that LIPH is a second causative gene for ARWH/hypotrichosis , giving rise to a phenotype clinically indistinguishable from P2RY5 mutations.
18830268
2009
×
Entrez Id:
200879
Gene Symbol:
LIPH
LIPH
0.500
GeneticVariation
disease
BEFREE
The effect of inbreeding on the distribution of compound heterozygotes: a lesson from Lipase H mutations in autosomal recessive woolly hair/hypotrichosis .
19365138
2009
×
Entrez Id:
10161
Gene Symbol:
LPAR6
LPAR6
0.500
GeneticVariation
disease
BEFREE
Mutations in LPAR6 /P2RY5 and LIPH are associated with woolly hair and/or hypotrichosis .
22385360
2013
×
Entrez Id:
200879
Gene Symbol:
LIPH
LIPH
0.500
GeneticVariation
disease
BEFREE
Sequence analysis of the LIPH gene revealed a novel nonsense mutation (p.Arg260X ) associated with hypotrichosis without woolly hair in one family.
23066499
2012
×
Entrez Id:
200879
Gene Symbol:
LIPH
LIPH
0.500
GeneticVariation
disease
BEFREE
The study further extends the body of evidence that sequence variants in the LIPH gene result in hypotrichosis and woolly hair phenotype.
26645693
2016
×
Entrez Id:
200879
Gene Symbol:
LIPH
LIPH
0.500
GeneticVariation
disease
BEFREE
The severity of hypotrichosis is known to be able to change in the clinical course, and the mutation patterns of LIPH do not always correlate with the severity of hypotrichosis in ARWH caused by other mutation sites of LIPH .
22449147
2013
×
Entrez Id:
200879
Gene Symbol:
LIPH
LIPH
0.500
GeneticVariation
disease
BEFREE
Autosomal recessive wooly hair/hypotrichosis phenotypes are mostly associated with pathogenic sequence variants in LIPH and LPAR6 genes.
31077348
2019
×
Entrez Id:
200879
Gene Symbol:
LIPH
LIPH
0.500
GeneticVariation
disease
LHGDN
This region contains the lipase H (LIPH ) gene which has been recently shown to underlie an autosomal-recessive form of hypotrichosis .
18830268
2009
×
Entrez Id:
10161
Gene Symbol:
LPAR6
LPAR6
0.500
GeneticVariation
disease
BEFREE
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
0.500
GeneticVariation
disease
LHGDN
Novel mutations in G protein-coupled receptor gene (P2RY5 ) in families with autosomal recessive hypotrichosis (LAH3).
18461368
2008
×
Entrez Id:
10161
Gene Symbol:
LPAR6
LPAR6
0.500
GeneticVariation
disease
BEFREE
It has recently been revealed that both LPAR6 and lipase H (LIPH) mutations cause autosomal recessive woolly hair (ARWH)/hypotrichosis .
21352330
2011
×
Entrez Id:
10161
Gene Symbol:
LPAR6
LPAR6
0.500
GeneticVariation
disease
BEFREE
Novel mutations in the P2RY5 gene in one Turkish and two Indian patients presenting with hypotrichosis and woolly hair.
19529952
2009
×
Entrez Id:
10161
Gene Symbol:
LPAR6
LPAR6
0.500
GeneticVariation
disease
BEFREE
Identification of an Alu-mediated 12.2-kb deletion of the complete LPAR6 (P2RY5 ) gene in a Turkish family with hypotrichosis and woolly hair.
22621192
2012
×
Entrez Id:
200879
Gene Symbol:
LIPH
LIPH
0.500
GeneticVariation
disease
LHGDN
A novel deletion mutation in LIPH gene causes autosomal recessive hypotrichosis (LAH2).
18445047
2008
×
Entrez Id:
10161
Gene Symbol:
LPAR6
LPAR6
0.500
GeneticVariation
disease
LHGDN
Our findings show that mutations in P2RY5 display variable expressivity, underlying both hypotrichosis and woolly hair, and underscore the essential role of P2RY5 in the tissue integrity and maintenance of the hair follicle.
18692127
2008
×
Entrez Id:
10161
Gene Symbol:
LPAR6
LPAR6
0.500
GeneticVariation
disease
LHGDN
[Involvement of receptor P2Y5 and its ligand LPA in hypotrichosis simplex and autosomal recessive wooly hair syndrome].
19061667
2008
×
Entrez Id:
200879
Gene Symbol:
LIPH
LIPH
0.500
GeneticVariation
disease
BEFREE
Mutations in lipase H (LIPH ) gene, located on chromosome 3q26.33, have been shown to be responsible for LAH2 type of hypotrichosis .
19167195
2009
×
Entrez Id:
200879
Gene Symbol:
LIPH
LIPH
0.500
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:
200879
Gene Symbol:
LIPH
LIPH
0.500
GeneticVariation
disease
BEFREE
In the Japanese populations, most patients with congenital woolly hair/hypotrichosis possess common founder mutations in the lipase H (LIPH ) gene.
22044263
2012
×
Entrez Id:
200879
Gene Symbol:
LIPH
LIPH
0.500
GeneticVariation
disease
BEFREE
It has recently been revealed that both LPAR6 and lipase H (LIPH ) mutations cause autosomal recessive woolly hair (ARWH)/hypotrichosis .
21352330
2011