|
| Entrez Id: |
5781 |
| Gene Symbol: |
PTPN11 |
PTPN11
|
0.500 |
Biomarker
|
disease |
CTD_human |
Germline gain-of-function mutations in RAF1 cause Noonan syndrome.
|
17603482 |
2007 |
|
| Entrez Id: |
5781 |
| Gene Symbol: |
PTPN11 |
PTPN11
|
0.500 |
Biomarker
|
disease |
CTD_human |
Cardiofaciocutaneous (CFC) syndrome associated with muscular coenzyme Q10 deficiency.
|
17703371 |
2007 |
|
| Entrez Id: |
5781 |
| Gene Symbol: |
PTPN11 |
PTPN11
|
0.500 |
Biomarker
|
disease |
CTD_human |
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy.
|
17603483 |
2007 |
|
| Entrez Id: |
5781 |
| Gene Symbol: |
PTPN11 |
PTPN11
|
0.500 |
Biomarker
|
disease |
CTD_human |
Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpn11 mutation.
|
15273746 |
2004 |
|
| Entrez Id: |
5781 |
| Gene Symbol: |
PTPN11 |
PTPN11
|
0.500 |
Biomarker
|
disease |
MGD |
Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpn11 mutation.
|
15273746 |
2004 |
|
| Entrez Id: |
1969 |
| Gene Symbol: |
EPHA2 |
EPHA2
|
0.300 |
Biomarker
|
disease |
CTD_human |
Regulation of apoptosis in HL-1 cardiomyocytes by phosphorylation of the receptor tyrosine kinase EphA2 and protection by lithocholic acid.
|
22845314 |
2012 |
|
| Entrez Id: |
4893 |
| Gene Symbol: |
NRAS |
NRAS
|
0.300 |
Biomarker
|
disease |
CTD_human |
A restricted spectrum of NRAS mutations causes Noonan syndrome.
|
19966803 |
2010 |
|
| Entrez Id: |
8036 |
| Gene Symbol: |
SHOC2 |
SHOC2
|
0.300 |
Biomarker
|
disease |
CTD_human |
Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair.
|
19684605 |
2009 |
|
| Entrez Id: |
3845 |
| Gene Symbol: |
KRAS |
KRAS
|
0.300 |
Biomarker
|
disease |
CTD_human |
Cardiofaciocutaneous (CFC) syndrome associated with muscular coenzyme Q10 deficiency.
|
17703371 |
2007 |
|
| Entrez Id: |
6654 |
| Gene Symbol: |
SOS1 |
SOS1
|
0.300 |
Biomarker
|
disease |
CTD_human |
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy.
|
17603483 |
2007 |
|
| Entrez Id: |
3845 |
| Gene Symbol: |
KRAS |
KRAS
|
0.300 |
Biomarker
|
disease |
CTD_human |
Germline gain-of-function mutations in RAF1 cause Noonan syndrome.
|
17603482 |
2007 |
|
| Entrez Id: |
673 |
| Gene Symbol: |
BRAF |
BRAF
|
0.300 |
Biomarker
|
disease |
CTD_human |
Cardiofaciocutaneous (CFC) syndrome associated with muscular coenzyme Q10 deficiency.
|
17703371 |
2007 |
|
| Entrez Id: |
5605 |
| Gene Symbol: |
MAP2K2 |
MAP2K2
|
0.300 |
Biomarker
|
disease |
CTD_human |
Cardiofaciocutaneous (CFC) syndrome associated with muscular coenzyme Q10 deficiency.
|
17703371 |
2007 |
|
| Entrez Id: |
5894 |
| Gene Symbol: |
RAF1 |
RAF1
|
0.300 |
Biomarker
|
disease |
CTD_human |
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy.
|
17603483 |
2007 |
|
| Entrez Id: |
5604 |
| Gene Symbol: |
MAP2K1 |
MAP2K1
|
0.300 |
Biomarker
|
disease |
CTD_human |
Cardiofaciocutaneous (CFC) syndrome associated with muscular coenzyme Q10 deficiency.
|
17703371 |
2007 |
|
| Entrez Id: |
3845 |
| Gene Symbol: |
KRAS |
KRAS
|
0.300 |
Biomarker
|
disease |
CTD_human |
Further evidence of genetic heterogeneity in Costello syndrome: involvement of the KRAS gene.
|
17468812 |
2007 |
|
| Entrez Id: |
3265 |
| Gene Symbol: |
HRAS |
HRAS
|
0.300 |
Biomarker
|
disease |
CTD_human |
Cardiofaciocutaneous (CFC) syndrome associated with muscular coenzyme Q10 deficiency.
|
17703371 |
2007 |
|
| Entrez Id: |
6654 |
| Gene Symbol: |
SOS1 |
SOS1
|
0.300 |
Biomarker
|
disease |
CTD_human |
Germline gain-of-function mutations in RAF1 cause Noonan syndrome.
|
17603482 |
2007 |
|
| Entrez Id: |
5894 |
| Gene Symbol: |
RAF1 |
RAF1
|
0.300 |
Biomarker
|
disease |
CTD_human |
Germline gain-of-function mutations in RAF1 cause Noonan syndrome.
|
17603482 |
2007 |
|
| Entrez Id: |
3845 |
| Gene Symbol: |
KRAS |
KRAS
|
0.300 |
Biomarker
|
disease |
CTD_human |
Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy.
|
17603483 |
2007 |