Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
790955
Gene name Gene Name - the full gene name approved by the HGNC.
Ubiquinol-cytochrome c reductase complex assembly factor 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
UQCC3
Synonyms (NCBI Gene) Gene synonyms aliases
C11orf83, CCDS41658.1, MC3DN9, UNQ655
Disease Acronyms (UniProt) Disease acronyms from UniProt database
MC3DN9
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q12.3
Summary Summary of gene provided in NCBI Entrez Gene.
Complex III is a mitochondrial inner membrane protein complex that transfers electrons from ubiquinol to cytochrome c. This gene encodes a protein that functions in complex III assembly. Mutations in this gene result in Mitochondrial complex III deficienc
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT753910 hsa-miR-1287-5p PAR-CLIP 26701625
MIRT753902 hsa-miR-1915-3p PAR-CLIP 26701625
MIRT753911 hsa-miR-25-5p PAR-CLIP 26701625
MIRT755162 hsa-miR-302f PAR-CLIP 26701625
MIRT753909 hsa-miR-3135b PAR-CLIP 26701625
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005654 Component Nucleoplasm IDA
GO:0005739 Component Mitochondrion IDA
GO:0005750 Component Mitochondrial respiratory chain complex III IBA 21873635
GO:0005750 Component Mitochondrial respiratory chain complex III IDA 25605331
GO:0005829 Component Cytosol IDA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
616097 34399 ENSG00000204922
Protein
UniProt ID Q6UW78
Protein name Ubiquinol-cytochrome-c reductase complex assembly factor 3 (Assembly factor CBP4 homolog)
Protein function Required for the assembly of the ubiquinol-cytochrome c reductase complex (mitochondrial respiratory chain complex III or cytochrome b-c1 complex), mediating cytochrome b recruitment and probably stabilization within the complex. Thereby, plays
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15141 UQCC3 1 91 Ubiquinol-cytochrome-c reductase complex assembly factor 3 Family
Sequence
Sequence length 93
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Developmental delay Global developmental delay rs28941770, rs199469464, rs281865469, rs143747297, rs398123009, rs587777428, rs786205133, rs606231459, rs797044854, rs797045027, rs864309504, rs878853160, rs886039902, rs886042046, rs886041291
View all (32 more)
Mitochondrial complex deficiency MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 9, MITOCHONDRIAL COMPLEX III DEFICIENCY (disorder) rs267606829, rs267606830, rs587776513, rs121918134, rs121918135, rs121918136, rs137853192, rs137853193, rs183973249, rs137853184, rs118203929, rs267606689, rs11544803, rs63751061, rs137852863
View all (210 more)
25008109, 28804536
Unknown
Disease term Disease name Evidence References Source
Mitochondrial Complex Deficiency mitochondrial complex III deficiency GenCC