rs121917878
|
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 |
rs121917878
|
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 |
rs121917878
|
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 |
rs121917878
|
SIX3;SIX3-AS1
|
HOLOPROSENCEPHALY 2 (disorder)
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in the human SIX3 gene in holoprosencephaly are loss of function.
|
18791198 |
2008 |
rs121917878
|
SIX3;SIX3-AS1
|
HOLOPROSENCEPHALY 2 (disorder)
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.
|
10369266 |
1999 |
rs121917878
|
SIX3;SIX3-AS1
|
HOLOPROSENCEPHALY 2 (disorder)
|
|
0.800 |
GeneticVariation |
UNIPROT |
SIX3 mutations with holoprosencephaly.
|
17001667 |
2006 |
rs121917879
|
SIX3;SIX3-AS1
|
HOLOPROSENCEPHALY 2 (disorder)
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in the human SIX3 gene in holoprosencephaly are loss of function.
|
18791198 |
2008 |
rs121917879
|
SIX3;SIX3-AS1
|
HOLOPROSENCEPHALY 2 (disorder)
|
|
0.800 |
GeneticVariation |
UNIPROT |
SIX3 mutations with holoprosencephaly.
|
17001667 |
2006 |
rs121917879
|
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 |
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 |