Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
4519
Gene name Gene Name - the full gene name approved by the HGNC.
Mitochondrially encoded cytochrome b
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CYTB
Synonyms (NCBI Gene) Gene synonyms aliases
MTCYB
Chromosome Chromosome number
MT
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
-
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT049965 hsa-miR-29a-3p CLASH 23622248
MIRT048433 hsa-miR-100-5p CLASH 23622248
MIRT045822 hsa-miR-140-5p CLASH 23622248
MIRT045100 hsa-miR-186-5p CLASH 23622248
MIRT042521 hsa-miR-423-3p CLASH 23622248
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001666 Process Response to hypoxia IEA
GO:0005739 Component Mitochondrion HDA 20833797
GO:0005739 Component Mitochondrion HTP 34800366
GO:0005739 Component Mitochondrion IEA
GO:0005743 Component Mitochondrial inner membrane IDA 28844695
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
516020 7427 HGNC
Protein
UniProt ID P00156
Protein name Cytochrome b (Complex III subunit 3) (Complex III subunit III) (Cytochrome b-c1 complex subunit 3) (Ubiquinol-cytochrome-c reductase complex cytochrome b subunit)
Protein function Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex) that is part of the mitochondrial respiratory chain. The b-c1 complex mediates electron transfer from ubiquinol to cytochrome c. Contributes to th
PDB 5XTE , 5XTH , 5XTI
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00033 Cytochrome_B 18 204 Cytochrome b/b6/petB Domain
PF00032 Cytochrom_B_C 258 359 Cytochrome b(C-terminal)/b6/petD Domain
Sequence
Sequence length 380
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Oxidative phosphorylation
Metabolic pathways
Cardiac muscle contraction
Thermogenesis
Non-alcoholic fatty liver disease
Alzheimer disease
Parkinson disease
Amyotrophic lateral sclerosis
Huntington disease
Prion disease
Pathways of neurodegeneration - multiple diseases
Chemical carcinogenesis - reactive oxygen species
Diabetic cardiomyopathy
  Respiratory electron transport
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