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Metazoan complexes |
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Details of UQCRB gene in Homo sapiens
IDs | |||||||||
---|---|---|---|---|---|---|---|---|---|
Link outs | Gene Name | Alias | Uniprot ID | SwissProt ID | NCBI gene ID | ENSEMBL ID | Description | Source | |
| UQCRB | UQBP | P14927 | QCR7_HUMAN | 7381 | ENSG00000156467 | Cytochrome b-c1 complex subunit 7 | SPROT |
Disease | |||||||||
---|---|---|---|---|---|---|---|---|---|
Disease | OMIM id | ||||||||
Mitochondrial complex III deficiency (MT-C3D) [MIM:124000]: A disorder of the mitochondrial respiratory chain resulting in a highly variable phenotype depending on which tissues are affected. Clinical features include mitochondrial encephalopathy, psychomotor retardation, ataxia, severe failure to thrive, liver dysfunction, renal tubulopathy, muscle weakness and exercise intolerance. Note=The disease is caused by mutations affecting the gene represented in this entry. | 124000 |
Phenotypes
Abnormal emotion/affect behavior, Abnormal fear/anxiety-related behavior, Abnormal glucose homeostasis, Abnormality of acid-base homeostasis, Abnormality of amino acid metabolism, Abnormality of blood and blood-forming tissues, Abnormality of blood glucose concentration, Abnormality of body weight, Abnormality of carbohydrate metabolism/homeostasis, Abnormality of carboxylic acid metabolism, Abnormality of central motor function, Abnormality of coagulation, Abnormality of coordination, Abnormality of higher mental function, Abnormality of metabolism/homeostasis, Abnormality of muscle fibers, Abnormality of muscle morphology, Abnormality of muscle physiology, Abnormality of the abdomen, Abnormality of the abdominal organs, Abnormality of the abdominal wall, Abnormality of the anterior segment of the eye, Abnormality of the biliary system, Abnormality of the cardiovascular system, Abnormality of the central nervous system, Abnormality of the cerebellum, Abnormality of the coagulation cascade, Abnormality of the ear, Abnormality of the eye, Abnormality of the fundus, Abnormality of the genitourinary system, Abnormality of the heart, Abnormality of the hindbrain, Abnormality of the lens, Abnormality of the liver, Abnormality of the metencephalon, Abnormality of the middle ear, Abnormality of the musculature, Abnormality of the myocardium, Abnormality of the nervous system, Abnormality of the posterior segment of the eye, Abnormality of the retina, Abnormality of the retinal pigment epithelium, Abnormality of the urinary system, Abnormality of the urinary system physiology, Abnormality of urine homeostasis, Abnormal muscle tone, Abnormal retinal pigmentation, Acidosis, Aciduria, All, Aminoaciduria, Ataxia, Autosomal recessive inheritance, Behavioural/Psychiatric Abnormality, Bilateral conductive hearing impairment, Cardiomyopathy, Cataract, Cerebellar atrophy, Cholestasis, Cognitive impairment, Conductive hearing impairment, Decreased body weight, Decreased liver function, Decreased mitochondrial complex III activity in liver tissue, Depression, EEG abnormality, Emotional lability, Encephalopathy, Exercise intolerance, Failure to thrive, Functional abnormality of the middle ear, Functional motor problems., Global developmental delay, Growth abnormality, Hallucinations, Hearing abnormality, Hearing impairment, Hepatic steatosis, Hypertrophic cardiomyopathy, Hypoglycemia, Increased serum lactate, Intellectual disability, Lactic acidosis, Malformation of the heart and great vessels, Metabolic acidosis, Microvesicular hepatic steatosis, Mitochondrial encephalopathy, Mitochondrial inheritance, Mode of inheritance, Morphological abnormality of the central nervous system, Muscle weakness, Muscular hypotonia, Neurophysiological abnormality, Onset and clinical course, Phenotypic abnormality, Phenotypic variability, Ragged-red muscle fibers, Retinitis pigmentosa, Rhabdomyolysis, Seizures.
Orthologs in other species | |||||||||
---|---|---|---|---|---|---|---|---|---|
M. musculus | D. melonogaster | C. elegans | S. purpuratus | ||||||
Uqcrb | --- | T02H6.11 | --- |
Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
Complex ID | Corum | BioGrid | IRefWeb | Novelty |
---|---|---|---|---|---|---|---|---|---|
UQCRB | ATP1A1 | 0.060283755 | UQCRB | ATP1A1 | cpx103 | no | no | no | Novel |
UQCRB | COX5A | 0.306385263 | UQCRB | COX5A | cpx218; cpx143 | no | yes | no | Known |
COX4I1 | UQCRB | 0.334524087 | COX4I1 | UQCRB | cpx218 | no | no | no | Novel |
ATP1B1 | UQCRB | 0.165177299 | ATP1B1 | UQCRB | cpx143; cpx103 | no | no | no | Novel |
UQCRFS1 | UQCRB | 0.02619646 | UQCRFS1 | UQCRB | cpx143 | no | yes | no | Known |
CYC1 | UQCRB | 0.135270587 | CYC1 | UQCRB | cpx143 | no | yes | no | Known |
ATP1B3 | UQCRB | 0.24696558 | ATP1B3 | UQCRB | cpx103 | no | no | no | Novel |
Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
---|---|---|---|---|
UQCRB | NDUFV1 | 0.07737529 | UQCRB | NDUFV1 |
UQCRB | VDAC1 | 0.073309459 | UQCRB | VDAC1 |
SDHB | UQCRB | 0.201751636 | SDHB | UQCRB |
NDUFA10 | UQCRB | 0.075722698 | NDUFA10 | UQCRB |
UQCRB | NDUFA8 | 0.078657805 | UQCRB | NDUFA8 |
VAPA | UQCRB | 0.077504258 | VAPA | UQCRB |
UQCRB | DDOST | 0.098980592 | UQCRB | DDOST |
NDUFS1 | UQCRB | 0.11351238 | NDUFS1 | UQCRB |
SDHA | UQCRB | 0.082756251 | SDHA | UQCRB |
UQCRB | NDUFA12 | 0.140781124 | UQCRB | NDUFA12 |
UQCRB | NDUFS4 | 0.087911273 | UQCRB | NDUFS4 |