Source: CURATED ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 Biomarker disease CLINGEN Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome. 23175444 2013
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 Biomarker disease CLINGEN Integrative genomic analysis reveals somatic mutations in pheochromocytoma and paraganglioma. 21784903 2011
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 Biomarker disease CLINGEN Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma. 16405730 2006
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 Biomarker disease CLINGEN Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene. 16249420 2005
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 Biomarker disease CLINGEN An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma. 15342702 2004
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 Biomarker disease CLINGEN Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC. 12658451 2003
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 Biomarker disease CLINGEN Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma. 11426453 2001
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 Biomarker disease CLINGEN Mutations in SDHC cause autosomal dominant paraganglioma, type 3. 11062460 2000
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.610 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 54949
Gene Symbol: SDHAF2
SDHAF2 		0.600 Biomarker disease CLINGEN Role of SDHAF2 and SDHD in von Hippel-Lindau associated pheochromocytomas. 24322175 2014
Entrez Id: 4149
Gene Symbol: MAX
MAX 		0.600 Biomarker disease CLINGEN Opposing effects of HIF1α and HIF2α on chromaffin cell phenotypic features and tumor cell proliferation: Insights from MYC-associated factor X. 24676840 2014
Entrez Id: 4149
Gene Symbol: MAX
MAX 		0.600 Biomarker disease CLINGEN A comprehensive next generation sequencing-based genetic testing strategy to improve diagnosis of inherited pheochromocytoma and paraganglioma. 23666964 2013
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.600 Biomarker disease CLINGEN Yeast model for evaluating the pathogenic significance of SDHB, SDHC and SDHD mutations in PHEO-PGL syndrome. 23175444 2013
Entrez Id: 4149
Gene Symbol: MAX
MAX 		0.600 Biomarker disease CLINGEN Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromes. 23551045 2013
Entrez Id: 4149
Gene Symbol: MAX
MAX 		0.600 Biomarker disease CLINGEN MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma. 22452945 2012
Entrez Id: 54949
Gene Symbol: SDHAF2
SDHAF2 		0.600 Biomarker disease CLINGEN Head and neck paragangliomas: genetic spectrum and clinical variability in 79 consecutive patients. 22241717 2012
Entrez Id: 4149
Gene Symbol: MAX
MAX 		0.600 Biomarker disease CLINGEN Mitochondrial function and content in pheochromocytoma/paraganglioma of succinate dehydrogenase mutation carriers. 22323561 2012
Entrez Id: 4149
Gene Symbol: MAX
MAX 		0.600 Biomarker disease GENOMICS_ENGLAND Pheochromocytoma and paraganglioma: understanding the complexities of the genetic background. 22429592 2012
Entrez Id: 4149
Gene Symbol: MAX
MAX 		0.600 Biomarker disease CLINGEN Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma. 21685915 2011
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.600 Biomarker disease CLINGEN Integrative genomic analysis reveals somatic mutations in pheochromocytoma and paraganglioma. 21784903 2011
Entrez Id: 54949
Gene Symbol: SDHAF2
SDHAF2 		0.600 Biomarker disease CLINGEN SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma. 20071235 2010
Entrez Id: 54949
Gene Symbol: SDHAF2
SDHAF2 		0.600 Biomarker disease CLINGEN SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma. 19628817 2009
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.600 Biomarker disease CLINGEN A HIF1alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas. 16103922 2005
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.600 Biomarker disease CLINGEN Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma. 12111639 2002
Entrez Id: 6392
Gene Symbol: SDHD
SDHD 		0.600 Biomarker disease CLINGEN Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene. 11391798 2001