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COQ4 (coenzyme Q4)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
51117
Gene nameGene Name - the full gene name approved by the HGNC.
Coenzyme Q4
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
COQ4
SynonymsGene synonyms aliases
CGI-92, COQ10D7, SPAX10
ChromosomeChromosome number
9
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
9q34.11
SummarySummary of gene provided in NCBI Entrez Gene.
This gene encodes a component of the coenzyme Q biosynthesis pathway. Coenzyme Q, an essential component of the electron transport chain, shuttles electrons between complexes I or II to complex III of the mitochondrial transport chain. This protein appear
SNPsSNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs141303335 A>G Likely-pathogenic Splice acceptor variant
rs143441644 C>T Pathogenic-likely-pathogenic, pathogenic 3 prime UTR variant, missense variant, genic downstream transcript variant, non coding transcript variant, coding sequence variant
rs530213004 G>A,C,T Pathogenic Synonymous variant, coding sequence variant, missense variant, non coding transcript variant
rs747779231 G>A,C,T Likely-pathogenic, pathogenic Splice donor variant
rs773943371 C>T Pathogenic, uncertain-significance, likely-pathogenic Coding sequence variant, non coding transcript variant, missense variant
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT035808 hsa-miR-1908-5p CLASH 23622248
MIRT904421 hsa-miR-1206 CLIP-seq
MIRT904422 hsa-miR-1225-5p CLIP-seq
MIRT904423 hsa-miR-22 CLIP-seq
MIRT904424 hsa-miR-3132 CLIP-seq
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25152161, 27499296, 32296183
GO:0005739 Component Mitochondrion IBA 21873635
GO:0005739 Component Mitochondrion IDA
GO:0006744 Process Ubiquinone biosynthetic process IEA
GO:0031314 Component Extrinsic component of mitochondrial inner membrane IEA
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID Q9Y3A0
Protein name Ubiquinone biosynthesis protein COQ4 homolog, mitochondrial (4-hydroxy-3-methoxy-5-polyprenylbenzoate decarboxylase) (EC 4.1.1.130) (Coenzyme Q biosynthesis protein 4 homolog)
Protein function Lyase that catalyzes the C1-decarboxylation of 4-hydroxy-3-methoxy-5-(all-trans-decaprenyl)benzoic acid into 2-methoxy-6-(all-trans-decaprenyl)phenol during ubiquinone biosynthesis. {ECO:0000255|HAMAP-Rule:MF_03111, ECO:0000269|PubMed:38295803,
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05019 Coq4
38 258
Coenzyme Q (ubiquinone) biosynthesis protein Coq4
Family
Sequence
Sequence length 265
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
  Ubiquinone and other terpenoid-quinone biosynthesis
Metabolic pathways
Biosynthesis of cofactors
 
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Coenzyme q10 deficiency COENZYME Q10 DEFICIENCY, PRIMARY, 7 rs118203955, rs121918230, rs121918231, rs121918233, rs751185256, rs864321686, rs750710187, rs1057519348, rs1558212305, rs1577993720 25658047, 26741492, 27604308, 26185144
Encephalomyopathy-cardiomyopathy-respiratory distress syndrome Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome rs774395996, rs775607037, rs143441644, rs786204770, rs786204771, rs758522459, rs886041549, rs747779231, rs767839639, rs776825296, rs1554796655, rs1045118320, rs141303335, rs1412692974
Multiple congenital anomalies Multiple congenital anomalies rs1057517732 18474229, 18579827, 25126048, 16116126, 24270420, 17332895, 21540551, 22368301, 25658047, 26185144, 17485248, 28540186, 21844807
Hypotonia Neonatal Hypotonia rs141138948, rs397517172, rs869312824, rs1583169151
Unknown
Disease name Disease term dbSNP ID References
Dysmorphic features Dysmorphic features 18474229, 22368301, 16116126, 21844807, 25126048, 18579827, 24270420, 17332895, 17485248, 25658047, 28540186, 26185144, 21540551
Dysphagia Deglutition Disorders

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