succinate dehydrogenase complex subunit C

Summary
Gene Symbol
  • SDHC
Aliases
  • CYB560
  • cybL
  • large subunit of cytochrome b
  • succinate dehydrgenase cytochrome b
  • succinate dehydrogenase cytochrome b560 subunit
Organism
Homo sapiens (human)
External Links
NCBI Gene
6391
HGNC
10682
KEGG Gene ID
hsa:6391
PubChem
6391
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Electron transport
  • Heme
  • Mitochondrion inner membrane
  • Reference proteome
  • Signal
  • Transit peptide
  • Transmembrane helix
  • Tricarboxylic acid cycle
Proteins
Displaying all 3 entries
UniProt Protein Name
A0A0S2Z4C9
A0A0S2Z4B7
Q99643
  • Integral membrane protein CII-3
  • Malate dehydrogenase [quinone] cytochrome b560 subunit
  • QPs-1
  • Succinate dehydrogenase complex subunit C
  • Succinate-ubiquinone oxidoreductase cytochrome B large subunit
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
KEGG BRITE Database
Orthology
K00236
Name
succinate dehydrogenase (ubiquinone) cytochrome b560 subunit
References
Disease
Disease Ontology
Displaying entries 1 - 10 of 190 in total
DO ID Disease Name Source
DOID:3178 skin papilloma
DOID:0050387 nonpapillary renal cell carcinoma
DOID:0050428 nonepidermolytic palmoplantar keratoderma
DOID:0050430 multiple endocrine neoplasia type 2A
DOID:0050471 Carney complex
DOID:0050486 exanthem
DOID:0050657 Bannayan-Riley-Ruvalcaba syndrome
DOID:0050771 pheochromocytoma
DOID:0050773 paraganglioma
DOID:0050955 spinocerebellar ataxia type 2
The Human Phenotype Ontology
Displaying entries 21 - 30 of 128 in total
HPO ID HPO Term
HP:0000790 Hematuria
HP:0000820 Abnormality of the thyroid gland
HP:0000853 Goiter
HP:0000953 Hyperpigmentation of the skin
HP:0000975 Hyperhidrosis
HP:0000980 Pallor
HP:0000982 Palmoplantar keratoderma
HP:0000988 Skin rash
HP:0000995 Melanocytic nevus
HP:0001025 Urticaria
Displaying all 7 entries
Disease ID Disease Name
OMIM:605373
  • paragangliomas 3
OMIM:606864
  • Carney-Stratakis syndrome
ORPHA:201
  • Cowden disease
ORPHA:97286
  • Carney-Stratakis syndrome
OMIM:606764
  • gastrointestinal stromal tumor
ORPHA:44890
  • gastrointestinal stromal tumor
ORPHA:29072
  • hereditary pheochromocytoma-paraganglioma

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024