Entrez Id: |
55654 |
Gene Symbol: |
TMEM127 |
TMEM127
|
Pheochromocytoma
|
0.800 |
GeneticVariation |
CLINVAR |
|
|
|
Entrez Id: |
55654 |
Gene Symbol: |
TMEM127 |
TMEM127
|
Pheochromocytoma
|
0.800 |
CausalMutation |
CLINVAR |
|
|
|
Entrez Id: |
55654 |
Gene Symbol: |
TMEM127 |
TMEM127
|
Hereditary Paraganglioma-Pheochromocytoma Syndrome
|
0.400 |
CausalMutation |
CLINVAR |
Novel SDHB and TMEM127 Mutations in Patients with Pheochromocytoma/Paraganglioma Syndrome.
|
26960314 |
2016 |
Entrez Id: |
55654 |
Gene Symbol: |
TMEM127 |
TMEM127
|
Hereditary Paraganglioma-Pheochromocytoma Syndrome
|
0.400 |
GeneticVariation |
CLINVAR |
Familial pheochromocytoma and renal cell carcinoma syndrome: TMEM127 as a novel candidate gene for the association.
|
25800244 |
2015 |
Entrez Id: |
55654 |
Gene Symbol: |
TMEM127 |
TMEM127
|
Hereditary Paraganglioma-Pheochromocytoma Syndrome
|
0.400 |
CausalMutation |
CLINVAR |
TMEM127 screening in a large cohort of patients with pheochromocytoma and/or paraganglioma.
|
22419703 |
2012 |
Entrez Id: |
55654 |
Gene Symbol: |
TMEM127 |
TMEM127
|
Hereditary Paraganglioma-Pheochromocytoma Syndrome
|
0.400 |
CausalMutation |
CLINVAR |
Identical germline mutations in the TMEM127 gene in two unrelated Japanese patients with bilateral pheochromocytoma.
|
22541004 |
2012 |
Entrez Id: |
55654 |
Gene Symbol: |
TMEM127 |
TMEM127
|
Hereditary Paraganglioma-Pheochromocytoma Syndrome
|
0.400 |
CausalMutation |
CLINVAR |
Germline mutations in TMEM127 confer susceptibility to pheochromocytoma.
|
20154675 |
2010 |
Entrez Id: |
55654 |
Gene Symbol: |
TMEM127 |
TMEM127
|
Hereditary Paraganglioma-Pheochromocytoma Syndrome
|
0.400 |
CausalMutation |
CLINVAR |
Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas.
|
21156949 |
2010 |
Entrez Id: |
55654 |
Gene Symbol: |
TMEM127 |
TMEM127
|
Neoplastic Syndromes, Hereditary
|
0.100 |
GeneticVariation |
CLINVAR |
Novel SDHB and TMEM127 Mutations in Patients with Pheochromocytoma/Paraganglioma Syndrome.
|
26960314 |
2016 |
Entrez Id: |
55654 |
Gene Symbol: |
TMEM127 |
TMEM127
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Novel SDHB and TMEM127 Mutations in Patients with Pheochromocytoma/Paraganglioma Syndrome.
|
26960314 |
2016 |
Entrez Id: |
55654 |
Gene Symbol: |
TMEM127 |
TMEM127
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Identical germline mutations in the TMEM127 gene in two unrelated Japanese patients with bilateral pheochromocytoma.
|
22541004 |
2012 |
Entrez Id: |
55654 |
Gene Symbol: |
TMEM127 |
TMEM127
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Germline mutations in TMEM127 confer susceptibility to pheochromocytoma.
|
20154675 |
2010 |
Entrez Id: |
55654 |
Gene Symbol: |
TMEM127 |
TMEM127
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas.
|
21156949 |
2010 |
Entrez Id: |
55654 |
Gene Symbol: |
TMEM127 |
TMEM127
|
PHEOCHROMOCYTOMA, SUSCEPTIBILITY TO
|
0.100 |
SusceptibilityMutation |
CLINVAR |
|
|
|