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COQ8A (coenzyme Q8A)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
56997
Gene nameGene Name - the full gene name approved by the HGNC.
Coenzyme Q8A
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
COQ8A
SynonymsGene synonyms aliases
ADCK3, ARCA2, CABC1, COQ10D4, COQ8, SCAR9
ChromosomeChromosome number
1
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1q42.13
SummarySummary of gene provided in NCBI Entrez Gene.
This gene encodes a mitochondrial protein similar to yeast ABC1, which functions in an electron-transferring membrane protein complex in the respiratory chain. It is not related to the family of ABC transporter proteins. Expression of this gene is induced
SNPsSNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs74589348 C>G,T Uncertain-significance, likely-benign, conflicting-interpretations-of-pathogenicity, benign Coding sequence variant, synonymous variant
rs119468004 G>A,C Pathogenic Missense variant, coding sequence variant
rs119468005 C>G,T Likely-pathogenic, pathogenic Missense variant, coding sequence variant
rs119468006 G>A,T Pathogenic Missense variant, coding sequence variant
rs119468008 A>G Pathogenic Missense variant, coding sequence variant
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004672 Function Protein kinase activity IDA 27499294
GO:0005515 Function Protein binding IPI 16189514, 25416956, 25910212, 27499296, 31515488, 32296183, 32814053
GO:0005524 Function ATP binding IEA
GO:0005739 Component Mitochondrion IDA 25498144
GO:0006468 Process Protein phosphorylation IDA 27499294
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID Q8NI60
Protein name Atypical kinase COQ8A, mitochondrial (EC 2.7.-.-) (Chaperone activity of bc1 complex-like) (Chaperone-ABC1-like) (Coenzyme Q protein 8A) (aarF domain-containing protein kinase 3)
Protein function Atypical kinase involved in the biosynthesis of coenzyme Q, also named ubiquinone, an essential lipid-soluble electron transporter for aerobic cellular respiration (PubMed:21296186, PubMed:25498144, PubMed:25540914, PubMed:27499294, PubMed:36302
PDB 4PED , 5I35 , 7UDP , 7UDQ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03109 ABC1
318 434
ABC1 family
Family
Sequence
MAAILGDTIMVAKGLVKLTQAAVETHLQHLGIGGELIMAARALQSTAVEQIGMFLGKVQG
QDKHEEYFAENFGGPEGEFHFSVPHAAGASTDFSSASAPDQSAPPSLGHAHSEGPAPAYV
ASGPFREAGFPGQASSPLGRANGRLFANPRDSFSAMGFQRRFFHQDQSPVGGLTAEDIEK
ARQAKARPENKQHKQTLSEHARERKVPVTRIGRLANFGGLAVGLGFGALAEVAKKSLRSE
DPSGKKAVLGSSPFLSEANAERIVRTLCKVRGAALKLGQMLSIQDDAFINPHLAKIFERV
RQSADFMPLKQMMKTLNNDLGPNWRDKLEYFEERPFAAASIGQVHLARMKGGREVAMKIQ
YPGVAQSINSDVNNLMAVLNMSNMLPEGLFPEHLIDVLRRELALECDYQREAACARKFRD
LLKGHPFFYVPEIV
DELCSPHVLTTELVSGFPLDQAEGLSQEIRNEICYNILVLCLRELF
EFHFMQTDPNWSNFFYDPQQHKVALLDFGATREYDRSFTDLYIQIIRAAADRDRETVRAK
SIEMKFLTGYEVKVMEDAHLDAILILGEAFASDEPFDFGTQSTTEKIHNLIPVMLRHRLV
PPPEETYSLHRKMGGSFLICSKLKARFPCKAMFEEAYSNYCKRQAQQ
Sequence length 647
Interactions View interactions
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Ataxia Autosomal recessive ataxia due to ubiquinone deficiency rs606231134, rs119103243, rs119103244, rs119103245, rs606231135, rs119468005, rs119468006, rs387906298, rs606231138, rs606231139, rs119468008, rs387906299, rs606231292, rs1553281318, rs794727986, rs1563130387, rs797045109, rs797045217, rs578189699, rs797046025, rs797046024, rs797046026, rs764847439, rs780451185, rs863224929, rs771578775, rs755933881, rs199874519, rs1085307053, rs886042265, rs201908721, rs747150601, rs1057519343, rs752130338, rs748118737, rs781518112, rs140246430, rs1554553667, rs1554573328, rs1554676394, rs1554753528, rs1203553546, rs1554829141, rs974677376, rs763325410, rs1554721227, rs1554226673, rs1554768245, rs1553280621, rs755531859, rs765966679, rs1554247806, rs750544827, rs768958602, rs1563941569, rs1564136499, rs1269308421, rs767584322, rs751637699, rs759460806, rs1271428051, rs752224921, rs1572040505, rs767406263, rs1590463470, rs771955377, rs1659738028
Cerebellar ataxia Progressive cerebellar ataxia rs28936415, rs199476133, rs540331226, rs797046006, rs863224069, rs138358708, rs1057519429, rs750959420, rs1568440440, rs1597846084, rs759460806, rs761486324, rs1240335250, rs1596489887
Coenzyme q10 deficiency COENZYME Q10 DEFICIENCY, COENZYME Q10 DEFICIENCY, PRIMARY, 1 rs118203955, rs121918230, rs121918231, rs121918233, rs751185256, rs864321686, rs750710187, rs1057519348, rs1558212305, rs1577993720 24896178, 27604308, 18319072
Developmental regression Developmental regression rs1224421127
Unknown
Disease name Disease term dbSNP ID References
Anxiety disorder Anxiety 29942085
Cerebellar atrophy Cerebellar atrophy
Gynecomastia Gynecomastia
Mitochondrial diseases Mitochondrial Diseases

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