×
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:
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
Biomarker
disease
BEFREE
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
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:
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
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:
10161
Gene Symbol:
LPAR6
LPAR6
0.500
AlteredExpression
disease
BEFREE
Using this technique with whole genome SNP data generated from low density mapping arrays, we previously identified two genes that underlie autosomal recessive woolly hair (ARWH/hypotrichosis ; OMIM278150), specifically P2RY5 and Lipase H (LIPH).
19365138
2009
×
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
×
Entrez Id:
10161
Gene Symbol:
LPAR6
LPAR6
0.500
GeneticVariation
disease
BEFREE
To search for pathogenic mutations in the human P2RY5 gene in Pakistani families with autosomal recessive hereditary hypotrichosis .
19292720
2009
×
Entrez Id:
200879
Gene Symbol:
LIPH
LIPH
0.500
GeneticVariation
disease
BEFREE
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:
147409
Gene Symbol:
DSG4
DSG4
0.350
GeneticVariation
disease
BEFREE
In addition, various mutations in the Dsg4 gene have been identified in animal models of hypotrichosis that share a characteristic phenotype called "lanceolate hair".
16439973
2006
×
Entrez Id:
147409
Gene Symbol:
DSG4
DSG4
0.350
GeneticVariation
disease
BEFREE
This study further extends the body of evidence that mutations in the DSG4 gene result in both hypotrichosis and monilethrix-like scalp hair.
25251037
2015
×
Entrez Id:
147409
Gene Symbol:
DSG4
DSG4
0.350
GeneticVariation
disease
BEFREE
The essential role of desmoglein 4 in skin was established by identifying mutations in families with inherited hypotrichosis , as well as in the lanceolate hair mouse.
12705872
2003