| HGNC Family | Mitochondrial respiratory chain complexes |
| Name | cytochrome b |
| Description | Predicted to enable metal ion binding activity. Predicted to contribute to ubiquinol-cytochrome-c reductase activity. Predicted to be involved in mitochondrial electron transport, ubiquinol to cytochrome c. Located in mitochondrion. Part of mitochondrial inner membrane. Implicated in ovarian carcinoma and urinary bladder cancer. [provided by Alliance of Genome Resources, Mar 2025] |
| Summary |
{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nMitochondrial cytochrome b (MT‑CYB) is a core subunit of complex III of the electron transport chain, serving as a pivotal mediator of electron transfer from ubiquinol to cytochrome c and thereby driving the proton‐motive force essential for ATP synthesis. Its precise assembly and function are critical for optimal mitochondrial bioenergetics, and mutations in MT‑CYB have been shown to disrupt complex III activity—often leading to isolated enzyme deficiencies, impaired oxidative phosphorylation, and altered apoptotic signaling. In patients, such mutations manifest as exercise intolerance, neuromuscular and multisystem involvement, and even tissue‐specific defects such as sensorineural hearing loss. Furthermore, studies employing biochemical, genetic, and functional assays have underscored the importance of MT‑CYB integrity not only for energy production but also for maintaining structural interactions with other respiratory complexes, as well as for modulating stress‐ and redox‐sensitive transcriptional responses."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "13"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nBeyond its indispensable role in cellular energy metabolism, variations in the MT‑CYB gene have been implicated in a broad spectrum of pathological conditions. Altered MT‑CYB function can compromise sperm mitochondrial activity—contributing to asthenozoospermia, fertilization failure, and male infertility—as well as participate in the pathogenesis of obesity‐related phenotypes. In addition, MT‑CYB mutations and sequence variations have been associated with diverse disease processes including certain cancers, atherosclerosis, fibromyalgia, and even aberrant immune responses; in one example, proteolytic fragments of cytochrome b have been shown to act as cryptides that activate neutrophils. These findings collectively highlight the dual importance of MT‑CYB both as an essential bioenergetic enzyme and as a modulator of cellular signaling and disease susceptibility."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "14", "end_ref": "26"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Tatsuya Yamasoba, Yu ichi Goto, Yoshitomo Oka, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Atypical muscle pathology and a survey of cis-mutations in deaf patients harboring a 1555 A-to-G point mutation in the mitochondrial ribosomal RNA gene."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Neuromuscul Disord (2002)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/s0960-8966(01)00329-7"}], "href": "https://doi.org/10.1016/s0960-8966(01"}, {"type": "t", "text": "00329-7) PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12031626"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12031626"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Masashi Tanaka, Noriyuki Fuku, Takeshi Takeyasu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Golden mean to longevity: rareness of mitochondrial cytochrome b variants in centenarians but not in patients with Parkinson's disease."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Neurosci Res (2002)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/jnr.10444"}], "href": "https://doi.org/10.1002/jnr.10444"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12391595"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12391595"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Michelangelo Mancuso, Massimiliano Filosto, J Clarke Stevens, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Neurol Sci (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/s0022-510x(02)00462-8"}], "href": "https://doi.org/10.1016/s0022-510x(02"}, {"type": "t", "text": "00462-8) PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12686403"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12686403"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Sandrine Haut, Thierry Billette de Villemeur, Michèle Brivet, et al. "}, {"type": "b", "children": [{"type": "t", "text": "The deleterious G15498A mutation in mitochondrial DNA-encoded cytochrome b may remain clinically silent in homoplasmic carriers."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Eur J Hum Genet (2004)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/sj.ejhg.5201132"}], "href": "https://doi.org/10.1038/sj.ejhg.5201132"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "14735157"}], "href": "https://pubmed.ncbi.nlm.nih.gov/14735157"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Emma L Blakely, Anna L Mitchell, Nicholas Fisher, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeast."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "FEBS J (2005)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/j.1742-4658.2005.04779.x"}], "href": "https://doi.org/10.1111/j.1742-4658.2005.04779.x"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "16008558"}], "href": "https://pubmed.ncbi.nlm.nih.gov/16008558"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Andrei P Komarov, Oskar W Rokhlin, Chang-An Yu, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "Evolutionary pressure on mitochondrial cytochrome b is consistent with a role of CytbI7T affecting longevity during caloric restriction."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS One (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pone.0005836"}], "href": "https://doi.org/10.1371/journal.pone.0005836"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19503808"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19503808"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Konstantina Fragaki, Vincent Procaccio, Sylvie Bannwarth, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "Liver mitochondrial DNA damage and genetic variability of Cytochrome b - a key component of the respirasome - drive the severity of fatty liver disease."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Intern Med (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1111/joim.13147"}], "href": "https://doi.org/10.1111/joim.13147"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32634278"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32634278"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "Ghulam Mohammad, Jay Kumar, Renu A Kowluru "}, {"type": "b", "children": [{"type": "t", "text": "Mitochondrial Genome-Encoded Long Noncoding RNA Cytochrome B and Mitochondrial Dysfunction in Diabetic Retinopathy."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Antioxid Redox Signal (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1089/ars.2023.0303"}], "href": "https://doi.org/10.1089/ars.2023.0303"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37464864"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37464864"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "Rosario Liguori, Cristina Mazzaccara, Fabrizio Pasanisi, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "Enhanced transcription of estrogen receptor α and mitochondrial cytochrome b genes in uterine leiomyomas."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Gynecol Endocrinol (2011)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3109/09513590.2011.569610"}], "href": "https://doi.org/10.3109/09513590.2011.569610"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "21506659"}], "href": "https://pubmed.ncbi.nlm.nih.gov/21506659"}]}, {"type": "r", "ref": 21, "children": [{"type": "t", "text": "Gen-Hong Mao, Ya-Nan Wang, Min Xu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Polymorphisms in the MT-ATP6 and MT-CYB genes in in vitro fertilization failure."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mitochondrial DNA (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.3109/19401736.2013.840612"}], "href": "https://doi.org/10.3109/19401736.2013.840612"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "24102627"}], "href": "https://pubmed.ncbi.nlm.nih.gov/24102627"}]}, {"type": "r", "ref": 22, "children": [{"type": "t", "text": "Mario D Cordero, Elísabet Alcocer-Gómez, Fabiola Marín-Aguilar, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "Mitochondria-related miR-151a-5p reduces cellular ATP production by targeting CYTB in asthenozoospermia."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Sci Rep (2015)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/srep17743"}], "href": "https://doi.org/10.1038/srep17743"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "26626315"}], "href": "https://pubmed.ncbi.nlm.nih.gov/26626315"}]}, {"type": "r", "ref": 24, "children": [{"type": "t", "text": "V V Sinyov, M M Chicheva, V A Barinova, et al. 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"}, {"type": "b", "children": [{"type": "t", "text": "Association between the single nucleotide variants of the mitochondrial cytochrome B gene (MT-CYB) and the male infertility."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Biol Rep (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s11033-022-07200-y"}], "href": "https://doi.org/10.1007/s11033-022-07200-y"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35118571"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35118571"}]}, {"type": "r", "ref": 26, "children": [{"type": "t", "text": "Yulia Yu Gromenko, Kamil S Galimov, Irina R Gilyazova, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Single nucleotide polymorphism rs527236194 of the cytochrome B gene (MT-CYB) is associated with alterations in sperm parameters."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Biol Rep (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s11033-023-08849-9"}], "href": "https://doi.org/10.1007/s11033-023-08849-9"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37921983"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37921983"}]}]}]}
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| Synonyms | CYTB, MTCYB |
| Proteins | CYB_HUMAN |
| NCBI Gene ID | 4519 |
| API | |
| Download Associations | |
| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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MT-CYB has 476 functional associations with biological entities spanning 6 categories (functional term, phrase or reference, disease, phenotype or trait, chemical, structural feature, cell line, cell type or tissue, gene, protein or microRNA) extracted from 21 datasets.
Click the + buttons to view associations for MT-CYB from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| CORUM Protein Complexes | protein complexs containing MT-CYB protein from the CORUM Protein Complexes dataset. | |
| CTD Gene-Disease Associations | diseases associated with MT-CYB gene/protein from the curated CTD Gene-Disease Associations dataset. | |
| DisGeNET Gene-Disease Associations | diseases associated with MT-CYB gene in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. | |
| DisGeNET Gene-Phenotype Associations | phenotypes associated with MT-CYB gene in GWAS and other genetic association datasets from the DisGeNET Gene-Phenoptype Associations dataset. | |
| ESCAPE Omics Signatures of Genes and Proteins for Stem Cells | PubMedIDs of publications reporting gene signatures containing MT-CYB from the ESCAPE Omics Signatures of Genes and Proteins for Stem Cells dataset. | |
| GAD Gene-Disease Associations | diseases associated with MT-CYB gene in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. | |
| GeneRIF Biological Term Annotations | biological terms co-occuring with MT-CYB gene in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. | |
| GEO Signatures of Differentially Expressed Genes for Diseases | disease perturbations changing expression of MT-CYB gene from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. | |
| GEO Signatures of Differentially Expressed Genes for Small Molecules | small molecule perturbations changing expression of MT-CYB gene from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset. | |
| GO Biological Process Annotations 2015 | biological processes involving MT-CYB gene from the curated GO Biological Process Annotations 2015 dataset. | |
| GO Cellular Component Annotations 2015 | cellular components containing MT-CYB protein from the curated GO Cellular Component Annotations 2015 dataset. | |
| GO Molecular Function Annotations 2015 | molecular functions performed by MT-CYB gene from the curated GO Molecular Function Annotations 2015 dataset. | |
| HPA Tissue Protein Expression Profiles | tissues with high or low expression of MT-CYB protein relative to other tissues from the HPA Tissue Protein Expression Profiles dataset. | |
| HPM Cell Type and Tissue Protein Expression Profiles | cell types and tissues with high or low expression of MT-CYB protein relative to other cell types and tissues from the HPM Cell Type and Tissue Protein Expression Profiles dataset. | |
| HPO Gene-Disease Associations | phenotypes associated with MT-CYB gene by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. | |
| HuGE Navigator Gene-Phenotype Associations | phenotypes associated with MT-CYB gene by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. | |
| InterPro Predicted Protein Domain Annotations | protein domains predicted for MT-CYB protein from the InterPro Predicted Protein Domain Annotations dataset. | |
| KEGG Pathways | pathways involving MT-CYB protein from the KEGG Pathways dataset. | |
| MiRTarBase microRNA Targets | microRNAs targeting MT-CYB gene in low- or high-throughput microRNA targeting studies from the MiRTarBase microRNA Targets dataset. | |
| PFOCR Pathway Figure Associations 2023 | pathways involving MT-CYB protein from the PFOCR Pathway Figure Associations 2023 dataset. | |
| WikiPathways Pathways 2014 | pathways involving MT-CYB protein from the Wikipathways Pathways 2014 dataset. | |