Gene Gene information from NCBI Gene database.
Entrez ID 728568
Gene name Ubiquinol-cytochrome c reductase complex assembly factor 6
Gene symbol UQCC6
Synonyms (NCBI Gene)
BRBRAWNINC12orf73
Chromosome 12
Chromosome location 12q23.3
miRNA miRNA information provided by mirtarbase database.
213
miRTarBase ID miRNA Experiments Reference
MIRT574861 hsa-miR-455-3p PAR-CLIP 20371350
MIRT574860 hsa-miR-5588-3p PAR-CLIP 20371350
MIRT574859 hsa-miR-1910-5p PAR-CLIP 20371350
MIRT574858 hsa-miR-186-3p PAR-CLIP 20371350
MIRT574857 hsa-miR-2052 PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
13
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32161263
GO:0005739 Component Mitochondrion HTP 34800366
GO:0005739 Component Mitochondrion IBA
GO:0005739 Component Mitochondrion IEA
GO:0005743 Component Mitochondrial inner membrane IDA 34969438
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
618812 34450 ENSG00000204954
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q69YU5
Protein name Ubiquinol-cytochrome c reductase complex assembly factor 6 (Protein BRAWNIN)
Protein function Required for the assembly and stability of the mitochondrial ubiquinol-cytochrome c reductase complex (complex III (CIII) or cytochrome b-c1 complex), a multisubunit transmembrane complex that is part of the mitochondrial electron transport chai
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14990 DUF4516 1 46 Domain of unknown function (DUF4516) Family
Tissue specificity TISSUE SPECIFICITY: Cardiac and skeletal muscle (at protein level). {ECO:0000269|PubMed:32161263}.
Sequence
Sequence length 71
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
SCHIZOPHRENIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Breast Neoplasms Breast neoplasm Pubtator 15387710 Associate
★☆☆☆☆
Found in Text Mining only