|
| Entrez Id: |
8820 |
| Gene Symbol: |
HESX1 |
HESX1
|
1.000 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
|
| Entrez Id: |
8820 |
| Gene Symbol: |
HESX1 |
HESX1
|
1.000 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
8820 |
| Gene Symbol: |
HESX1 |
HESX1
|
1.000 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
|
| Entrez Id: |
128674 |
| Gene Symbol: |
PROKR2 |
PROKR2
|
0.420 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
2260 |
| Gene Symbol: |
FGFR1 |
FGFR1
|
0.420 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
6658 |
| Gene Symbol: |
SOX3 |
SOX3
|
0.420 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
6657 |
| Gene Symbol: |
SOX2 |
SOX2
|
0.410 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
9915 |
| Gene Symbol: |
ARNT2 |
ARNT2
|
0.400 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
5015 |
| Gene Symbol: |
OTX2 |
OTX2
|
0.400 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
5626 |
| Gene Symbol: |
PROP1 |
PROP1
|
0.150 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
2736 |
| Gene Symbol: |
GLI2 |
GLI2
|
0.110 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
5449 |
| Gene Symbol: |
POU1F1 |
POU1F1
|
0.110 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
8022 |
| Gene Symbol: |
LHX3 |
LHX3
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
6091 |
| Gene Symbol: |
ROBO1 |
ROBO1
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
7473 |
| Gene Symbol: |
WNT3 |
WNT3
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
340419 |
| Gene Symbol: |
RSPO2 |
RSPO2
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
55717 |
| Gene Symbol: |
WDR11 |
WDR11
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
89884 |
| Gene Symbol: |
LHX4 |
LHX4
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
50937 |
| Gene Symbol: |
CDON |
CDON
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
23432 |
| Gene Symbol: |
GPR161 |
GPR161
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
|
| Entrez Id: |
57148 |
| Gene Symbol: |
RALGAPB |
RALGAPB
|
0.100 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|
|
| Entrez Id: |
4519 |
| Gene Symbol: |
CYTB |
CYTB
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Septo-optic dysplasia associated with a new mitochondrial cytochrome b mutation.
|
11891837 |
2002 |
|
| Entrez Id: |
8820 |
| Gene Symbol: |
HESX1 |
HESX1
|
1.000 |
GermlineCausalMutation
|
disease |
ORPHANET |
Septo-optic dysplasia and other midline defects: the role of transcription factors: HESX1 and beyond.
|
21396578 |
2011 |
|
| Entrez Id: |
8820 |
| Gene Symbol: |
HESX1 |
HESX1
|
1.000 |
AlteredExpression
|
disease |
BEFREE |
Septo-optic dysplasia and other midline defects: the role of transcription factors: HESX1 and beyond.
|
21396578 |
2011 |
|
| Entrez Id: |
5077 |
| Gene Symbol: |
PAX3 |
PAX3
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Septo-optic dysplasia and WS1 in the proband of a WS1 family segregating for a novel mutation in PAX3 exon 7.
|
9541113 |
1998 |