Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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51117 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Coenzyme Q4 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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COQ4 |
SynonymsGene synonyms aliases
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CGI-92, COQ10D7, SPAX10 |
ChromosomeChromosome number
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9 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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9q34.11 |
SummarySummary of gene provided in NCBI Entrez Gene.
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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.
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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 |
rs774395996 |
C>G,T |
Pathogenic |
Genic downstream transcript variant, coding sequence variant, missense variant, non coding transcript variant, intron variant |
rs775607037 |
C>A,T |
Pathogenic |
Synonymous variant, genic downstream transcript variant, coding sequence variant, non coding transcript variant, stop gained, intron variant |
rs786204771 |
CCA>- |
Pathogenic |
Genic downstream transcript variant, coding sequence variant, non coding transcript variant, inframe deletion, intron variant |
rs1045118320 |
C>A |
Likely-pathogenic, pathogenic |
Intron variant, missense variant, coding sequence variant, genic downstream transcript variant, non coding transcript variant |
rs1163170578 |
T>G |
Likely-pathogenic, uncertain-significance |
Coding sequence variant, genic downstream transcript variant, missense variant, non coding transcript variant, intron variant |
rs1412692974 |
G>T |
Pathogenic |
Coding sequence variant, missense variant, non coding transcript variant |
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miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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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 |
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Sequence |
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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.
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Associated diseases
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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 |
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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 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Dysmorphic features |
Dysmorphic features |
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18474229, 22368301, 16116126, 21844807, 25126048, 18579827, 24270420, 17332895, 17485248, 25658047, 28540186, 26185144, 21540551 |
Dysphagia |
Deglutition Disorders |
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