rs112535818
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
Hair Color
G
0.700
GeneticVariation
GWASCAT
Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability.
30531825
2018
rs139073416
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1
T
0.800
CausalMutation
CLINVAR
rs139073416
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1
A
0.800
CausalMutation
CLINVAR
Phenotypic variability in hyperphosphatasia with seizures and neurologic deficit (Mabry syndrome).
22315194
2012
rs139073416
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1
A
0.800
CausalMutation
CLINVAR
Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome.
20802478
2010
rs139073416
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1
A
0.800
CausalMutation
CLINVAR
Hyperphosphatasia-mental retardation syndrome due to PIGV mutations: expanded clinical spectrum.
21739589
2011
rs139073416
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1
0.800
GeneticVariation
UNIPROT
Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome.
20802478
2010
rs139073416
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1
A
0.800
CausalMutation
CLINVAR
Delineation of PIGV mutation spectrum and associated phenotypes in hyperphosphatasia with mental retardation syndrome.
24129430
2014
rs139073416
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1
A
0.800
CausalMutation
CLINVAR
Mechanism for release of alkaline phosphatase caused by glycosylphosphatidylinositol deficiency in patients with hyperphosphatasia mental retardation syndrome.
22228761
2012
rs139073416
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
Long philtrum
A
0.700
CausalMutation
CLINVAR
rs139073416
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
Hyperphosphatasia with Mental Retardation
A
0.700
GeneticVariation
CLINVAR
Phenotypic variability in hyperphosphatasia with seizures and neurologic deficit (Mabry syndrome).
22315194
2012
rs139073416
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
Thin upper lip vermilion
A
0.700
CausalMutation
CLINVAR
rs139073416
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
Hyperphosphatasia with Mental Retardation
A
0.700
GeneticVariation
CLINVAR
Delineation of PIGV mutation spectrum and associated phenotypes in hyperphosphatasia with mental retardation syndrome.
24129430
2014
rs139073416
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
Hyperphosphatasia with Mental Retardation
A
0.700
GeneticVariation
CLINVAR
Hyperphosphatasia-mental retardation syndrome due to PIGV mutations: expanded clinical spectrum.
21739589
2011
rs139073416
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
Seizures
A
0.700
CausalMutation
CLINVAR
rs139073416
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
Hyperphosphatasia with Mental Retardation
A
0.700
GeneticVariation
CLINVAR
Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome.
20802478
2010
rs139073416
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
Hyperphosphatasia with Mental Retardation
A
0.700
GeneticVariation
CLINVAR
Mechanism for release of alkaline phosphatase caused by glycosylphosphatidylinositol deficiency in patients with hyperphosphatasia mental retardation syndrome.
22228761
2012
rs139073416
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
Upward slant of palpebral fissure
A
0.700
CausalMutation
CLINVAR
rs139073416
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
Global developmental delay
A
0.700
CausalMutation
CLINVAR
rs139073416
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
Serum alkaline phosphatase raised
A
0.700
CausalMutation
CLINVAR
rs139073416
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
Short nose
A
0.700
CausalMutation
CLINVAR
rs1450982775
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
Hyperphosphatasia with Mental Retardation
0.010
GeneticVariation
BEFREE
We developed a diagnostic gene panel for targeting all known genes encoding proteins in the GPI-anchor-synthesis pathway to screen individuals matching these features, and we detected three missense mutations in PGAP2, c.46C>T, c.380T>C , and c.479C>T, in two unrelated individuals with hyperphosphatasia with mental retardation syndrome (HPMRS).
23561847
2013
rs146091102
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
Neutrophil count (procedure)
A
0.700
GeneticVariation
GWASCAT
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
27863252
2016
rs146091102
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
Blood basophil count (lab test)
A
0.700
GeneticVariation
GWASCAT
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
27863252
2016
rs267606951
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1
C
0.800
CausalMutation
CLINVAR
rs267606951
×
Entrez Id:
55650
Gene Symbol:
PIGV
PIGV
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1
0.800
GeneticVariation
UNIPROT
Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome.
20802478
2010