×
Entrez Id:
7466
Gene Symbol:
WFS1
WFS1
0.980
CausalMutation
disease
CLINVAR
Replication of the association between variants in WFS1 and risk of type 2 diabetes in European populations.
18040659
2008
×
Entrez Id:
7466
Gene Symbol:
WFS1
WFS1
0.980
CausalMutation
disease
CLINVAR
Common variants in WFS1 confer risk of type 2 diabetes.
17603484
2007
×
Entrez Id:
7466
Gene Symbol:
WFS1
WFS1
0.980
Biomarker
disease
BEFREE
We detected an 8.3 Mb terminal deletion and an adjacent 2.6 Mb inverted duplication in the short arm of chromosome 4, which encompasses a gene associated with WFS (WFS1 ).
17637805
2007
×
Entrez Id:
7466
Gene Symbol:
WFS1
WFS1
0.980
GeneticVariation
disease
UNIPROT
Wolfram syndrome in French population: characterization of novel mutations and polymorphisms in the WFS1 gene.
15605410
2005
×
Entrez Id:
7466
Gene Symbol:
WFS1
WFS1
0.980
Biomarker
disease
MGD
Disruption of the WFS1 gene in mice causes progressive beta-cell loss and impaired stimulus-secretion coupling in insulin secretion.
15056606
2004
×
Entrez Id:
7466
Gene Symbol:
WFS1
WFS1
0.980
Biomarker
disease
BEFREE
The WFS1 (Wolfram syndrome 1 ) is not a major susceptibility gene for the development of psychiatric disorders.
12605098
2003
×
Entrez Id:
7466
Gene Symbol:
WFS1
WFS1
0.980
GeneticVariation
disease
UNIPROT
Identification of novel WFS1 mutations in Italian children with Wolfram syndrome.
11295831
2001
×
Entrez Id:
7466
Gene Symbol:
WFS1
WFS1
0.980
GeneticVariation
disease
UNIPROT
Presence of a major WFS1 mutation in Spanish Wolfram syndrome pedigrees.
11161832
2001
×
Entrez Id:
7466
Gene Symbol:
WFS1
WFS1
0.980
CausalMutation
disease
CLINVAR
Identification of novel WFS1 mutations in Italian children with Wolfram syndrome.
11295831
2001
×
Entrez Id:
7466
Gene Symbol:
WFS1
WFS1
0.980
GeneticVariation
disease
UNIPROT
Clinical and molecular genetic analysis of 19 Wolfram syndrome kindreds demonstrating a wide spectrum of mutations in WFS1.
10521293
1999
×
Entrez Id:
7466
Gene Symbol:
WFS1
WFS1
0.980
GeneticVariation
disease
UNIPROT
Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein.
9817917
1998
×
Entrez Id:
7466
Gene Symbol:
WFS1
WFS1
0.980
CausalMutation
disease
CLINVAR
Evidence of an increased risk of hearing loss in heterozygous carriers in a Wolfram syndrome family.
9856492
1998
×
Entrez Id:
7466
Gene Symbol:
WFS1
WFS1
0.980
Biomarker
disease
GENOMICS_ENGLAND
Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein.
9817917
1998
×
Entrez Id:
7466
Gene Symbol:
WFS1
WFS1
0.980
GeneticVariation
disease
UNIPROT
A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome).
9771706
1998
×
Entrez Id:
7466
Gene Symbol:
WFS1
WFS1
0.980
Biomarker
disease
GENOMICS_ENGLAND