|
| Entrez Id: |
7050 |
| Gene Symbol: |
TGIF1 |
TGIF1
|
0.600 |
Biomarker
|
disease |
CTD_human |
Embryonic fibroblasts from mice lacking Tgif were defective in cell cycling.
|
16705179 |
2006 |
|
| Entrez Id: |
7050 |
| Gene Symbol: |
TGIF1 |
TGIF1
|
0.600 |
GermlineCausalMutation
|
disease |
ORPHANET |
|
|
|
|
| Entrez Id: |
7050 |
| Gene Symbol: |
TGIF1 |
TGIF1
|
0.600 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
2736 |
| Gene Symbol: |
GLI2 |
GLI2
|
0.500 |
Biomarker
|
disease |
CTD_human |
Gli2 gene-environment interactions contribute to the etiological complexity of holoprosencephaly: evidence from a mouse model.
|
27585885 |
2016 |
|
| Entrez Id: |
6469 |
| Gene Symbol: |
SHH |
SHH
|
0.500 |
Biomarker
|
disease |
CTD_human |
Gli2 gene-environment interactions contribute to the etiological complexity of holoprosencephaly: evidence from a mouse model.
|
27585885 |
2016 |
|
| Entrez Id: |
6469 |
| Gene Symbol: |
SHH |
SHH
|
0.500 |
Biomarker
|
disease |
CTD_human |
NODAL and SHH dose-dependent double inhibition promotes an HPE-like phenotype in chick embryos.
|
23264560 |
2013 |
|
| Entrez Id: |
4838 |
| Gene Symbol: |
NODAL |
NODAL
|
0.500 |
Biomarker
|
disease |
CTD_human |
NODAL and SHH dose-dependent double inhibition promotes an HPE-like phenotype in chick embryos.
|
23264560 |
2013 |
|
| Entrez Id: |
6469 |
| Gene Symbol: |
SHH |
SHH
|
0.500 |
Biomarker
|
disease |
CTD_human |
Gas1 is a modifier for holoprosencephaly and genetically interacts with sonic hedgehog.
|
17525797 |
2007 |
|
| Entrez Id: |
2619 |
| Gene Symbol: |
GAS1 |
GAS1
|
0.500 |
Biomarker
|
disease |
CTD_human |
Gas1 is a modifier for holoprosencephaly and genetically interacts with sonic hedgehog.
|
17525797 |
2007 |
|
| Entrez Id: |
6469 |
| Gene Symbol: |
SHH |
SHH
|
0.500 |
Biomarker
|
disease |
CTD_human |
Wide phenotypic variability in families with holoprosencephaly and a sonic hedgehog mutation.
|
15107988 |
2004 |
|
| Entrez Id: |
6997 |
| Gene Symbol: |
TDGF1 |
TDGF1
|
0.500 |
Biomarker
|
disease |
CTD_human |
A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects.
|
12073012 |
2002 |
|
| Entrez Id: |
6496 |
| Gene Symbol: |
SIX3 |
SIX3
|
0.500 |
Biomarker
|
disease |
CTD_human |
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.
|
10369266 |
1999 |
|
| Entrez Id: |
6496 |
| Gene Symbol: |
SIX3 |
SIX3
|
0.500 |
GermlineCausalMutation
|
disease |
ORPHANET |
|
|
|
|
| Entrez Id: |
6469 |
| Gene Symbol: |
SHH |
SHH
|
0.500 |
GermlineCausalMutation
|
disease |
ORPHANET |
|
|
|
|
| Entrez Id: |
2736 |
| Gene Symbol: |
GLI2 |
GLI2
|
0.500 |
GermlineCausalMutation
|
disease |
ORPHANET |
|
|
|
|
| Entrez Id: |
4838 |
| Gene Symbol: |
NODAL |
NODAL
|
0.500 |
GermlineCausalMutation
|
disease |
ORPHANET |
|
|
|
|
| Entrez Id: |
2619 |
| Gene Symbol: |
GAS1 |
GAS1
|
0.500 |
GermlineCausalMutation
|
disease |
ORPHANET |
|
|
|
|
| Entrez Id: |
6997 |
| Gene Symbol: |
TDGF1 |
TDGF1
|
0.500 |
GermlineCausalMutation
|
disease |
ORPHANET |
|
|
|
|
| Entrez Id: |
2260 |
| Gene Symbol: |
FGFR1 |
FGFR1
|
0.400 |
GermlineCausalMutation
|
disease |
ORPHANET |
Mutational Spectrum in Holoprosencephaly Shows That FGF is a New Major Signaling Pathway.
|
27363716 |
2016 |
|
| Entrez Id: |
5727 |
| Gene Symbol: |
PTCH1 |
PTCH1
|
0.400 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
5727 |
| Gene Symbol: |
PTCH1 |
PTCH1
|
0.400 |
GermlineCausalMutation
|
disease |
ORPHANET |
|
|
|
|
| Entrez Id: |
2253 |
| Gene Symbol: |
FGF8 |
FGF8
|
0.400 |
GermlineCausalMutation
|
disease |
ORPHANET |
|
|
|
|
| Entrez Id: |
2253 |
| Gene Symbol: |
FGF8 |
FGF8
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|
|
| Entrez Id: |
7546 |
| Gene Symbol: |
ZIC2 |
ZIC2
|
0.400 |
GermlineCausalMutation
|
disease |
ORPHANET |
|
|
|
|
| Entrez Id: |
2260 |
| Gene Symbol: |
FGFR1 |
FGFR1
|
0.400 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|