rs121917879
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.800
GeneticVariation
UNIPROT
Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations.
15221788
2004
rs121917879
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.800
GeneticVariation
UNIPROT
Functional characterization of SIX3 homeodomain mutations in holoprosencephaly: interaction with the nuclear receptor NR4A3/NOR1.
15523651
2004
rs121917879
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.800
GeneticVariation
UNIPROT
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.
10369266
1999
rs121917880
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.800
GeneticVariation
UNIPROT
The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes.
20531442
2010
rs121917880
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.800
GeneticVariation
UNIPROT
Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations.
15221788
2004
rs121917880
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.800
GeneticVariation
UNIPROT
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.
10369266
1999
rs121917880
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.800
GeneticVariation
UNIPROT
SIX3 mutations with holoprosencephaly.
17001667
2006
rs121917880
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.800
GeneticVariation
UNIPROT
Functional characterization of SIX3 homeodomain mutations in holoprosencephaly: interaction with the nuclear receptor NR4A3/NOR1.
15523651
2004
rs121917880
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.800
GeneticVariation
UNIPROT
Mutations in the human SIX3 gene in holoprosencephaly are loss of function.
18791198
2008
rs137853021
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.800
GeneticVariation
UNIPROT
Functional characterization of SIX3 homeodomain mutations in holoprosencephaly: interaction with the nuclear receptor NR4A3/NOR1.
15523651
2004
rs137853021
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.800
GeneticVariation
UNIPROT
SIX3 mutations with holoprosencephaly.
17001667
2006
rs137853021
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.800
GeneticVariation
UNIPROT
The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes.
20531442
2010
rs137853021
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.800
GeneticVariation
UNIPROT
Mutations in the human SIX3 gene in holoprosencephaly are loss of function.
18791198
2008
rs137853021
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.800
GeneticVariation
UNIPROT
Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations.
15221788
2004
rs137853021
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.800
GeneticVariation
UNIPROT
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.
10369266
1999
rs387906868
SIX3;SIX3-AS1
Schizencephaly
0.800
GeneticVariation
UNIPROT
Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly.
20157829
2010
rs121917881
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.700
GeneticVariation
UNIPROT
Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations.
15221788
2004
rs121917881
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.700
GeneticVariation
UNIPROT
Mutations in the human SIX3 gene in holoprosencephaly are loss of function.
18791198
2008
rs121917881
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.700
GeneticVariation
UNIPROT
SIX3 mutations with holoprosencephaly.
17001667
2006
rs121917881
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.700
GeneticVariation
UNIPROT
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.
10369266
1999
rs121917881
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.700
GeneticVariation
UNIPROT
Functional characterization of SIX3 homeodomain mutations in holoprosencephaly: interaction with the nuclear receptor NR4A3/NOR1.
15523651
2004
rs121917881
SIX3;SIX3-AS1
HOLOPROSENCEPHALY 2 (disorder)
0.700
GeneticVariation
UNIPROT
The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes.
20531442
2010
rs780942050
×
Entrez Id:
6496
Gene Symbol:
SIX3
SIX3
HOLOPROSENCEPHALY 2 (disorder)
0.700
GeneticVariation
UNIPROT
Mutations in the human SIX3 gene in holoprosencephaly are loss of function.
18791198
2008
rs780942050
×
Entrez Id:
6496
Gene Symbol:
SIX3
SIX3
HOLOPROSENCEPHALY 2 (disorder)
0.700
GeneticVariation
UNIPROT
Functional characterization of SIX3 homeodomain mutations in holoprosencephaly: interaction with the nuclear receptor NR4A3/NOR1.
15523651
2004
rs780942050
×
Entrez Id:
6496
Gene Symbol:
SIX3
SIX3
HOLOPROSENCEPHALY 2 (disorder)
0.700
GeneticVariation
UNIPROT
The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes.
20531442
2010