Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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14501 to 14510 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

14501
Ubiquinol-cytochrome c reductase, complex III subunit X
HSPC051, HSPC119, HSPC151, QCR9, UCCR7.2, UCRC
Ankylosing spondylitis, Crohn disease, Psoriasis, Sclerosing cholangitis, Diabetes mellitus type 2, Ulcerative colitis

14502
Ubiquinol-cytochrome c reductase binding protein
MC3DN3, QCR7, QP-C, QPC, UQBC, UQBP, UQCR6, UQPC
Diverticular disease, Mitochondrial complex deficiency, Diabetes mellitus type 2

14503
Ubiquinol-cytochrome c reductase core protein 1
D3S3191, PKNPY, QCR1, UQCR1
Alzheimer disease, Bone fracture, Hypertrophic cardiomyopathy, Parkinsonism with polyneuropathy

14504
Ubiquinol-cytochrome c reductase core protein 2
MC3DN5, QCR2, UQCR2
Mitochondrial complex deficiency, Mitochondrial disease, Obesity, Venous thromboembolism

14505
Ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1
MC3DN10, RIP1, RIS1, RISP, UQCR5
Alzheimer disease, Cardiomyopathy, Dementia, Mitochondrial complex deficiency, Myocardial ischemia

14506
Ubiquinol-cytochrome c reductase hinge protein
MC3DN11, QCR6, UQCR8
Alzheimer disease, Mitochondrial complex deficiency

14507
Ubiquinol-cytochrome c reductase complex III subunit VII
MC3DN4, QCR8, QP-C, QPC, UQCR7
Leigh syndrome, Mitochondrial complex deficiency

14508
Ureidoimidazoline (2-oxo-4-hydroxy-4-carboxy-5-) decarboxylase
PRHOXNB
Major depressive disorder, Peptic ulcer disease

14509
URB1 ribosome biogenesis factor
C21orf108, NPA1
Glucocorticoid deficiency, Squamous cell carcinoma

14510
URB2 ribosome biogenesis homolog
KIAA0133, NET10, NPA2
Epilepsy