Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 Biomarker disease CTD_human
Entrez Id: 6391
Gene Symbol: SDHC
SDHC 		0.300 Biomarker disease CTD_human
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 GeneticVariation disease CLINVAR How general practitioners manage depressive illness: developing a method of audit. 7143317 1982
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 GeneticVariation disease CLINVAR The effect of some anti-inflammatory agents on elastase release from neutrophils in-vitro. 1980289 1990
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 GeneticVariation disease CLINVAR Age-related changes of the ciliary muscle in comparison with changes induced by treatment with prostaglandin F2 alpha. An ultrastructural study in rhesus and cynomolgus monkeys. 2308387 1990
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Effects of compression on physiologic integrity of the spinal cord, on circulation, and clinical status in four different directions of compression: posterior, anterior, circumferential, and lateral. 1523504 1992
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. 11404820 2001
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 GeneticVariation disease UNIPROT Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. 11404820 2001
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Germ-line mutations in nonsyndromic pheochromocytoma. 12000816 2002
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 GeneticVariation disease UNIPROT Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas. 11897817 2002
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 GeneticVariation disease CLINVAR Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas. 12618761 2003
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 GeneticVariation disease UNIPROT Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility. 14974914 2003
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas. 12618761 2003
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas. 14500403 2003
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 GeneticVariation disease CLINVAR Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas. 14500403 2003
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 GeneticVariation disease UNIPROT A novel succinate dehydrogenase subunit B gene mutation, H132P, causes familial malignant sympathetic extraadrenal paragangliomas. 14715873 2004
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 GeneticVariation disease CLINVAR Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. 15328326 2004
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. 15328326 2004
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 GeneticVariation disease UNIPROT Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. 15328326 2004
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Genetic testing in pheochromocytoma or functional paraganglioma. 16314641 2005
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 CausalMutation disease CLINVAR Accumulation of Krebs cycle intermediates and over-expression of HIF1alpha in tumours which result from germline FH and SDH mutations. 15987702 2005
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 GeneticVariation disease CLINVAR Genetic testing in pheochromocytoma or functional paraganglioma. 16314641 2005
Entrez Id: 7799
Gene Symbol: PRDM2
PRDM2 		0.010 AlteredExpression disease BEFREE A panel of 18 pheochromocytomas (14 benign, and 4 malignant) and 11 abdominal paragangliomas (4 benign, and 7 malignant) were characterised for somatic deletions and mRNA expression status of RIZ1 using loss of heterozygosity (LOH) analysis and real-time quantitative PCR, respectively. 15809732 2005
Entrez Id: 6390
Gene Symbol: SDHB
SDHB 		0.710 GeneticVariation disease CLINVAR High frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas: implications for genetic testing. 16912137 2006