COQ2
type: Thing
description: protein-coding gene in the species Homo sapiens
additional property: PropertyValue
  property ID: P31
  value: gene
additional property: PropertyValue
  property ID: P279
  value: protein-coding gene
additional property: PropertyValue
  property ID: P351
  value: 27235
additional property: PropertyValue
  property ID: P353
  value: COQ2
additional property: PropertyValue
  property ID: P354
  value: 25223
additional property: PropertyValue
  property ID: P492
  value: 609825
additional property: PropertyValue
  property ID: P593
  value: 69192
additional property: PropertyValue
  property ID: P594
  value: ENSG00000173085
additional property: PropertyValue
  property ID: P639
  value: NM_015697
additional property: PropertyValue
  property ID: P639
  value: NM_001358921
additional property: PropertyValue
  property ID: P644
  value: 83261536
additional property: PropertyValue
  property ID: P644
  value: 84182689
additional property: PropertyValue
  property ID: P645
  value: 83284914
additional property: PropertyValue
  property ID: P645
  value: 84206067
additional property: PropertyValue
  property ID: P646
  value: /m/03hgkgf
additional property: PropertyValue
  property ID: P684
  value: Coq2
additional property: PropertyValue
  property ID: P684
  value: COQ2
additional property: PropertyValue
  property ID: P684
  value: Coq2
additional property: PropertyValue
  property ID: P688
  value: Coenzyme Q2, polyprenyltransferase
additional property: PropertyValue
  property ID: P692
  value: PBB GE COQ2 213379 at fs.png
additional property: PropertyValue
  property ID: P703
  value: Homo sapiens
additional property: PropertyValue
  property ID: P704
  value: ENST00000514935
additional property: PropertyValue
  property ID: P704
  value: ENST00000311461
additional property: PropertyValue
  property ID: P704
  value: ENST00000311469
additional property: PropertyValue
  property ID: P1057
  value: human chromosome 4
additional property: PropertyValue
  property ID: P2293
  value: coenzyme Q10 deficiency disease
additional property: PropertyValue
  property ID: P2293
  value: multiple system atrophy
additional property: PropertyValue
  property ID: P2293
  value: Leigh syndrome with nephrotic syndrome
additional property: PropertyValue
  property ID: P2548
  value: reverse strand
additional property: PropertyValue
  property ID: P2888
  value: http://identifiers.org/ncbigene/27235
confidence:
  popularity graph score:
    score: 0.002
    score pct: 0
    tier: established
    components:
      sitelinks: 0
      sitelinks norm: 0.0
      unique citations: 11
      unique citations norm: 0.004
      monthly pageviews: 17
      monthly pageviews norm: 0.0
  sitelinks: 0
  unique citations: 11
  monthly pageviews: 17
  yearly pageviews: 26
  pageview trend:
    m: 2026-08
    v: 17
  pageview trend:
    m: 2026-07
    v: 5
  pageview trend:
    m: 2026-06
    v: 3
  pageview trend:
    m: 2026-05
    v: 1
  tier: established
claims:
  P31:
    value: Q7187
    source count: 1
    confidence: 0.2
    value label: gene
  P279:
    value: Q20747295
    source count: 1
    confidence: 0.2
    value label: protein-coding gene
  P351:
    value: 27235
    source count: 1
    confidence: 0.2
  P353:
    value: COQ2
    source count: 1
    confidence: 0.2
  P354:
    value: 25223
    source count: 1
    confidence: 0.2
  P492:
    value: 609825
    source count: 1
    confidence: 0.2
  P593:
    value: 69192
    source count: 1
    confidence: 0.2
  P594:
    value: ENSG00000173085
    source count: 1
    confidence: 0.2
  P639:
    value: NM_015697
    source count: 1
    confidence: 0.2
  P639:
    value: NM_001358921
    source count: 1
    confidence: 0.2
  P644:
    value: 83261536
    source count: 1
    confidence: 0.2
  P644:
    value: 84182689
    source count: 1
    confidence: 0.2
  P645:
    value: 83284914
    source count: 1
    confidence: 0.2
  P645:
    value: 84206067
    source count: 1
    confidence: 0.2
  P646:
    value: /m/03hgkgf
    source count: 0
    confidence: 0.0
  P684:
    value: Q18265137
    source count: 2
    confidence: 0.4
    value label: Coq2
  P684:
    value: Q27544805
    source count: 1
    confidence: 0.2
    value label: COQ2
  P684:
    value: Q24407830
    source count: 2
    confidence: 0.4
    value label: Coq2
  P684:
    value: Q29708642
    source count: 2
    confidence: 0.4
    value label: Coq2

value: Q29671372
source count: 2
confidence: 0.4
value label: coq-2

value: Q21111976
source count: 1
confidence: 0.2
value label: Coenzyme Q2, polyprenyltransferase

value: PBB GE COQ2 213379 at fs.png
source count: 0
confidence: 0.0

value: Q15978631
source count: 1
confidence: 0.2
value label: Homo sapiens

value: ENST00000514935
source count: 1
confidence: 0.2

value: ENST00000311461
source count: 1
confidence: 0.2

value: ENST00000311469
source count: 1
confidence: 0.2

value: ENST00000503391
source count: 1
confidence: 0.2

value: ENST00000503915
source count: 1
confidence: 0.2

value: Q836605
source count: 1
confidence: 0.2
value label: human chromosome 4

value: Q5140809
source count: 1
confidence: 0.2
value label: coenzyme Q10 deficiency disease

value: Q1541975
source count: 1
confidence: 0.2
value label: multiple system atrophy

value: Q56013896
source count: 1
confidence: 0.2
value label: Leigh syndrome with nephrotic syndrome

value: Q22809711
source count: 1
confidence: 0.2
value label: reverse strand

value: http://identifiers.org/ncbigene/27235
source count: 1
confidence: 0.2

value: C1824776
source count: 1
confidence: 0.2

value: 4q21.23
source count: 1
confidence: 0.2

value: Q66601980
source count: 1
confidence: 0.2
value label: Skeletal muscle tissue of biceps brachii

value: Q66601955
source count: 1
confidence: 0.2
value label: Skeletal muscle tissue of rectus abdominis

value: Q66558726
source count: 1
confidence: 0.2
value label: gingival epithelium

value: Q975459
source count: 1
confidence: 0.2
value label: vastus lateralis muscle

value: Q107244
source count: 1
confidence: 0.2
value label: monocyte

source: Open Targets Platform
stated in qid: Q113138000
retrieved: 2023-08-24

source: Bgee
stated in qid: Q54985720
retrieved: 2024-06-07

source: Orthologous MAtrix
stated in qid: Q7104801

source: Identifiers.org
stated in qid: Q16335166

source: Q20641742
stated in qid: Q20641742
retrieved: 2022-05-15

source: Online Mendelian Inheritance in Man
stated in qid: Q241953
retrieved: 2019-08-19

source: UniProt
stated in qid: Q905695
retrieved: 2017-07-06

source: UMLS 2023
stated in qid: Q118645236
retrieved: 2023-06-15

source: ensembl Release 106
stated in qid: Q111699881

source: Ensembl Release 87
stated in qid: Q27975061

source: HomoloGene build68
stated in qid: Q20976936

wikidata id: Q18038726
domain: gene
level: standard
html url: https://4ort.xyz/entity/coq2
markdown url: https://4ort.xyz/entity/coq2.md
facts url summary: https://4ort.xyz/entity/coq2/facts.json
facts url standard: https://4ort.xyz/entity/coq2/facts.json
facts url full: https://4ort.xyz/entity/coq2/facts.json
data source: Wikidata (CC0 / public domain)
license: https://creativecommons.org/publicdomain/zero/1.0/
api version: v1
served at: 2026-08-20T10:21:16.969955Z
entity updated at: 2026-05-03T18:28:36.114423+00:00Z
entity created at: 2026-05-03T14:39:58.913405+00:00Z