- AARS2 1
- AASS 1
- ABAT 1
- ABCA1 1
- ABCB11 1
- ABCB4 1
- ABCB7 2
- ABCD1 2
- ABCD4 1
- ABCG5 1
- ABCG8 1
- ABHD12 1
- ABHD5 1
- ACAD8 1
- ACAD9 2
- ACADM 2
- ACADS 1
- ACADSB 1
- ACADVL 2
- ACAT1 0
- ACO2 1
- ACOX1 1
- ACSF3 1
- ACY1 1
- ADA 3
- ADAR 1
- ADSL 1
- AFG3L2 0
- AGA 1
- AGK 0
- AGL 1
- AGPS 0
- AGXT 0
- AHCY 2
- AIFM1 0
- AKR1D1 1
- ALAD 1
- ALAS2 1
- ALDH18A1 1
- ALDH3A2 1
- ALDH4A1 1
- ALDH5A1 1
- ALDH6A1 1
- ALDH7A1 2
- ALDOA 1
- ALDOB 0
- ALG1 0
- ALG11 0
- ALG12 0
- ALG14 1
- ALG3 0
- ALG6 0
- ALG8 0
- ALG9 0
- ALPL 1
- AMACR 0
- AMN 1
- AMT 1
- ANO10 0
- APOA1 1
- APOA5 1
- APOB 1
- APOC2 1
- APOE 1
- APOPT1 1
- APRT 1
- APTX 0
- ARG1 0
- ARSA 1
- ARSB 0
- ARSE 1
- ASAH1 1
- ASL 0
- ASPA 1
- ASS1 0
- ATAD3A 4
- ATIC 2
- ATP13A2 1
- ATP5A1 3
- ATP5E 2
- ATP6AP1 0
- ATP6V0A2 0
- ATP7A 3
- ATP7B 1
- ATP8B1 1
- ATPAF2 0
- AUH 0
- B3GALNT2 0
- B3GALT6 0
- B3GAT3 0
- B3GLCT 1
- B4GALT1 0
- B4GALT7 0
- BAAT 1
- BCKDHA 0
- BCKDHB 0
- BCKDK 1
- BCS1L 0
- BOLA3 0
- BTD 0
- C12orf65 1
- C19orf12 1
- CA5A 1
- CAT 0
- CBS 2
- CCDC115 1
- CHCHD10 1
- CHKB 0
- CHST14 0
- CHST3 0
- CHST6 0
- CHSY1 0
- CISD2 1
- CLDN16 1
- CLDN19 1
- CLN3 1
- CLN5 1
- CLN6 1
- CLN8 1
- CLPB 1
- CLPP 0
- CNNM2 1
- COG1 0
- COG4 0
- COG5 0
- COG6 0
- COG7 0
- COG8 0
- COQ2 1
- COQ4 0
- COQ6 0
- COQ7 1
- COQ8A 1
- COQ8B 1
- COQ9 0
- COX10 0
- COX14 0
- COX15 0
- COX20 0
- COX6A1 0
- COX6B1 0
- COX7B 0
- CP 1
- CPOX 3
- CPS1 0
- CPT1A 0
- CPT2 2
- CTH 1
- CTNS 1
- CTSA 1
- CTSC 1
- CTSD 1
- CTSK 1
- CUBN 1
- CYC1 0
- CYP27A1 1
- CYP7B1 1
- D2HGDH 1
- DARS 1
- DARS2 0
- DBH 2
- DBT 0
- DCXR 2
- DDC 2
- DGUOK 0
- DHCR24 1
- DHCR7 2
- DHFR 0
- DHODH 1
- DHTKD1 1
- DLAT 0
- DLD 0
- DNA2 0
- DNAJC12 1
- DNAJC19 2
- DNAJC5 1
- DNM1L 0
- DNM2 1
- DOLK 0
- DPAGT1 0
- DPM1 0
- DPM2 1
- DPM3 3
- DPYD 2
- DPYS 1
- DYM 0
- EARS2 0
- EBP 1
- ECHS1 0
- ELAC2 0
- ENO3 2
- EPG5 1
- EPM2A 1
- ETFA 1
- ETFB 2
- ETFDH 1
- ETHE1 0
- EXT1 0
- EXT2 0
- FA2H 1
- FAH 1
- FAR1 0
- FARS2 0
- FASTKD2 0
- FBP1 0
- FBXL4 0
- FDX2 1
- FECH 2
- FGFR2 1
- FH 0
- FKRP 0
- FKTN 0
- FMO3 2
- FOLR1 0
- FOXRED1 0
- FTCD 2
- FUCA1 1
- FUT8 1
- FXN 1
- G6PC 1
- G6PC3 1
- GAA 2
- GABRG2 1
- GALC 1
- GALE 1
- GALK1 1
- GALNS 0
- GALNT3 0
- GALT 1
- GAMT 2
- GARS 1
- GATM 0
- GBA 1
- GBE1 1
- GCDH 1
- GCH1 1
- GCLC 1
- GDAP1 1
- GFER 0
- GFM1 0
- GFPT1 0
- GIF 2
- GK 1
- GLA 0
- GLB1 0
- GLDC 1
- GLRA1 1
- GLRX5 0
- GLUD1 0
- GLUL 1
- GLYCTK 1
- GM2A 1
- GMPPB 0
- GNE 0
- GNMT 1
- GNPAT 0
- GNPTAB 0
- GNPTG 0
- GNS 0
- GPD1 1
- GPHN 1
- GRHPR 0
- GSS 1
- GTPBP3 0
- GUSB 0
- GYG1 2
- GYS1 2
- GYS2 0
- HAAO 1
- HADH 1
- HADHA 1
- HADHB 1
- HAMP 1
- HARS2 2
- HCCS 0
- HCFC1 1
- HEXA 1
- HEXB 1
- HFE 1
- HFE2 2
- HGD 1
- HGSNAT 0
- HIBCH 0
- HLCS 0
- HMBS 2
- HMGCL 0
- HMGCS2 1
- HOGA1 0
- HPD 1
- HPRT1 1
- HPS1 1
- HS2ST1 1
- HSD17B10 1
- HSD17B4 0
- HSD3B7 2
- HSPD1 0
- HTRA2 1
- HYAL1 2
- IARS2 1
- IBA57 0
- IDH2 2
- IDS 0
- IDUA 0
- IER3IP1 2
- ISCA2 1
- ISCU 2
- ISPD 1
- ITPA 1
- IVD 0
- KARS 1
- KYNU 2
- L2HGDH 1
- LAMP2 2
- LARGE1 2
- LARS 1
- LARS2 0
- LBR 1
- LCAT 1
- LCT 1
- LDHA 1
- LDLR 1
- LDLRAP1 1
- LIAS 0
- LIPA 1
- LIPT1 0
- LMBRD1 1
- LONP1 0
- LPIN1 2
- LPL 1
- LRPPRC 0
- LYRM4 2
- MAGT1 1
- MAN1B1 0
- MAN2B1 1
- MANBA 1
- MAOA 1
- MARS2 1
- MAT1A 2
- MCCC1 1
- MCCC2 1
- MCEE 0
- MCOLN1 0
- MFF 1
- MFN2 0
- MFSD8 1
- MGAT2 0
- MGME1 0
- MLYCD 0
- MMAA 0
- MMAB 0
- MMACHC 1
- MMADHC 1
- MOCS1 1
- MOCS2 1
- MOGS 1
- MPDU1 0
- MPI 0
- MPV17 0
- MRPL3 2
- MRPS22 0
- MSMO1 1
- MT-ATP6 0
- MT-ATP8 0
- MT-CO1 0
- MT-CO2 0
- MT-CO3 0
- MT-CYB 0
- MTFMT 1
- MTHFR 0
- MT-ND1 0
- MT-ND2 0
- MT-ND3 0
- MT-ND4 1
- MT-ND4L 0
- MT-ND5 0
- MT-ND6 0
- MTO1 0
- MTPAP 3
- MTR 1
- MT-RNR1 1
- MTRR 1
- MT-TA 1
- MT-TC 0
- MT-TD 0
- MT-TE 0
- MT-TF 0
- MT-TG 0
- MT-TH 0
- MT-TI 0
- MT-TK 0
- MT-TL1 0
- MT-TL2 0
- MT-TM 0
- MT-TN 0
- MTTP 1
- MT-TP 0
- MT-TQ 0
- MT-TR 0
- MT-TS1 0
- MT-TS2 0
- MT-TV 0
- MT-TW 0
- MT-TY 0
- MUT 1
- MVK 1
- NAGA 1
- NAGLU 0
- NAGS 0
- NARS2 0
- NDUFA1 1
- NDUFA10 0
- NDUFA11 0
- NDUFA12 3
- NDUFA2 0
- NDUFAF1 0
- NDUFAF2 0
- NDUFAF3 0
- NDUFAF4 0
- NDUFAF5 0
- NDUFAF6 1
- NDUFB11 0
- NDUFB3 0
- NDUFC2 1
- NDUFS1 0
- NDUFS2 0
- NDUFS3 0
- NDUFS4 0
- NDUFS6 0
- NDUFS7 0
- NDUFS8 0
- NDUFV1 0
- NDUFV2 0
- NEU1 0
- NFU1 0
- NGLY1 1
- NHLRC1 1
- NNT 1
- NPC1 1
- NPC2 1
- NSDHL 1
- NT5C3A 1
- NUBPL 0
- OAT 0
- OCRL 2
- OGDH 2
- OPA1 0
- OPA3 0
- OTC 1
- OXCT1 0
- PAH 1
- PANK2 1
- PC 0
- PCBD1 1
- PCCA 0
- PCCB 0
- PCK1 2
- PCSK9 1
- PDHA1 0
- PDHB 0
- PDHX 0
- PDP1 0
- PDSS1 0
- PDSS2 0
- PEPD 1
- PET100 0
- PEX1 0
- PEX10 0
- PEX11B 0
- PEX12 0
- PEX13 0
- PEX14 0
- PEX16 0
- PEX19 0
- PEX2 0
- PEX26 0
- PEX3 0
- PEX5 0
- PEX6 1
- PEX7 0
- PFKM 2
- PGAM2 2
- PGAP2 0
- PGAP3 0
- PGK1 2
- PGM1 1
- PGM3 0
- PHGDH 1
- PHKA1 2
- PHKA2 0
- PHKB 1
- PHKG2 0
- PHYH 0
- PIGA 0
- PIGL 0
- PIGM 3
- PIGN 0
- PIGO 0
- PIGT 1
- PIGV 0
- PINK1 1
- PLA2G6 1
- PMM2 0
- PMPCA 0
- PNP 1
- PNPO 1
- PNPT1 0
- POLG 1
- POLG2 2
- POMGNT1 0
- POMGNT2 0
- POMT1 0
- POMT2 0
- POR 1
- PPA2 0
- PPOX 2
- PPT1 1
- PRKAG2 2
- PRODH 2
- PRPS1 1
- PSAP 0
- PSAT1 1
- PTS 2
- PUS1 1
- PYCR1 0
- PYGL 0
- PYGM 1
- QDPR 1
- RARS2 0
- RBCK1 2
- RBP4 2
- RFT1 0
- RMND1 0
- RNASEH1 0
- RPIA 2
- RPL10 1
- RRM2B 1
- SACS 0
- SAMHD1 0
- SAR1B 2
- SARS2 0
- SC5D 2
- SCO1 0
- SCO2 0
- SCP2 0
- SDHA 1
- SDHAF1 0
- SDHB 1
- SDHD 0
- SEC23B 1
- SERAC1 0
- SETX 2
- SGSH 0
- SI 2
- SKIV2L 2
- SLC12A3 2
- SLC16A1 1
- SLC17A5 1
- SLC18A2 2
- SLC19A2 0
- SLC19A3 0
- SLC22A5 2
- SLC25A1 1
- SLC25A12 2
- SLC25A13 0
- SLC25A15 0
- SLC25A19 0
- SLC25A20 0
- SLC25A22 0
- SLC25A26 0
- SLC25A3 1
- SLC25A38 0
- SLC25A4 1
- SLC25A46 0
- SLC2A1 2
- SLC2A2 0
- SLC30A10 1
- SLC35A1 2
- SLC35A2 3
- SLC35C1 0
- SLC35D1 0
- SLC37A4 1
- SLC39A14 1
- SLC39A4 2
- SLC39A8 1
- SLC3A1 2
- SLC40A1 1
- SLC46A1 0
- SLC52A2 2
- SLC52A3 1
- SLC5A1 2
- SLC6A19 3
- SLC6A3 2
- SLC6A8 2
- SLC7A7 0
- SLC7A9 2
- SMPD1 1
- SPG7 1
- SPR 2
- SPTLC1 2
- SPTLC2 2
- SRD5A3 0
- SSR4 0
- ST3GAL3 2
- ST3GAL5 0
- STS 2
- SUCLA2 1
- SUCLG1 0
- SUMF1 1
- SUOX 1
- SURF1 0
- TACO1 0
- TALDO1 1
- TANGO2 1
- TAT 2
- TAZ 1
- TCN2 2
- TFR2 1
- TIMM8A 0
- TK2 1
- TMEM165 0
- TMEM5 1
- TMEM70 0
- TPK1 0
- TPP1 1
- TRAP1 1
- TREX1 2
- TRIM37 0
- TRMU 0
- TRNT1 0
- TRPM6 1
- TSFM 1
- TTC19 0
- TTC37 2
- TTPA 2
- TUFM 2
- TUSC3 0
- TWNK 2
- TYMP 1
- UGT1A1 3
- UMOD 2
- UMPS 1
- UQCRB 3
- UROD 1
- UROS 2
- VARS2 0
- VIPAS39 2
- VKORC1 2
- VPS33B 2
- WDR45 1
- WFS1 3
- XDH 1
- XYLT1 1
- XYLT2 0
- YARS2 0
- ALG13 1
- COX4I2 1
- CSTB 1
- DHDDS 1
- GLS 3
- HSPA9 1
- LIPC 2
- MRPS16 2
- NDUFB9 2
- OPLAH 2
- PDK3 2
- PSPH 1
- RANBP2 2
- RNASET2 1
- RYR1 1
- SDHAF2 2
- SDHC 2
- STAT2 1
- TH 2
- UQCRQ 1
- UROC1 1
- ABCG2 1
- ALG2 1
- AMPD1 2
- AOX1 1
- ARSG 1
- ATXN7 2
- BCAT1 1
- BCAT2 2
- C1GALT1C1 1
- CD320 1
- CETP 1
- CLPS 1
- CNDP1 1
- COA5 1
- COX8A 1
- CYP7A1 1
- DHFR2 1
- DLST 2
- DMGDH 1
- DPEP1 1
- EGF 1
- FOLR2 1
- FOLR3 1
- FXYD2 1
- GALNT12 1
- GCSH 2
- GGT1 2
- HAL 1
- HYKK 1
- KHK 1
- LFNG 1
- LIPI 1
- MRPL12 1
- MTHFD1 1
- NAT8L 1
- NDUFA9 1
- NT5C 1
- NUP62 1
- PDK1 2
- PDK2 1
- PDK4 1
- PDP2 1
- PDPR 3
- PDXK 1
- PEX11A 1
- PHKG1 1
- PHYKPL 1
- PNLIP 1
- PPM1B 1
- PPM1K 1
- PREPL 2
- PTPRZ1 1
- RNASEH2A 2
- RNASEH2B 2
- RNASEH2C 2
- SARDH 1
- SCARB1 1
- SHPK 1
- SLC22A4 1
- SLC25A2 1
- SLC27A5 1
- SLC36A2 2
- SLC52A1 1
- SLC6A20 1
- SLCO1B1 1
- SLCO1B3 1
- SUCLG2 1
- SUGCT 1
- TCN1 2
- TDO2 1
- TM6SF2 1
- TMEM126A 2
- TPMT 1
- TREH 1
- UPB1 2
- USF1 1
- HIBADH 1
Undiagnosed metabolic disorders
Gene: COQ4 Green List (high evidence)EnsemblGeneIds (GRCh38): ENSG00000167113
EnsemblGeneIds (GRCh37): ENSG00000167113
OMIM: 612898, Gene2Phenotype
COQ4 is in 15 panels
0 reviews
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Literature
- Phenotypes
-
- Coenzyme Q10 deficiency, primary, 7, OMIM:616276
- OMIM
- 612898
- Clinvar variants
- Variants in COQ4
- Penetrance
- Complete
- Publications
- Panels with this gene
-
- Childhood onset dystonia, chorea or related movement disorder
- Rhabdomyolysis and metabolic muscle disorders
- Mitochondrial disorders
- Early onset or syndromic epilepsy
- DDG2P
- Intellectual disability
- Retinal disorders
- Likely inborn error of metabolism
- Hereditary ataxia with onset in adulthood
- Acute rhabdomyolysis
- Ataxia and cerebellar anomalies - narrow panel
- Possible mitochondrial disorder - nuclear genes
- Adult onset hereditary spastic paraplegia
- Fetal anomalies
- Undiagnosed metabolic disorders
History Filter Activity
Set Phenotypes
Achchuthan Shanmugasundram (Genomics England Curator)Phenotypes for gene: COQ4 were changed from Disorders of CoQ10 biosynthesis (Mitochondrial respiratory chain disorders (caused by nuclear variants only)); Coenzyme Q10 deficiency, primary, 7; Disorders of ubiquinone metabolism and biosynthesis to Coenzyme Q10 deficiency, primary, 7, OMIM:616276
panel promoted to version 1
Sarah Leigh (Genomics England Curator)Construction of “Undiagnosed Metabolic Disorders” (UDM) panel • The 614 genes from the neurometabolic gene panel (PMID: 27604308) added • Green genes downloaded from V1 metabolic panels (Cerebral folate deficiency, Congenital disorders of glycosylation, Hyperammonaemia, Ketotic hypoglycaemia, Mitochondrial disorders, Mucopolysaccharideosis, Gaucher, Fabry, Peroxisomal disorders), sources replaced with "Expert review green", then loaded as a review onto UDM panel, resulting in 367 green genes and 333 red (therefore 86 new green genes included from the additional metabolic panels that weren't previously on the UDM panel) • Downloaded green genes from all panels. Removed genes from none V1 panels. Removed genes from the metabolic panels mentioned above. Compared the remaining genes with the red genes from UDM panel. Loaded as an "Expert review Amber" review to the overlapping genes, (the panel name where the genes came from was used as the phenotype) • Used variant information from PMID 27604308 to review the genes on this panel • Reviewed genes on UDM panel with genes from Emory "Inherited Metabolic Disorders: Sequencing Panel" and UKGTN “Inborn Errors of Metabolism 226 panel”, changing status where appropriate, added 14 UKGTN genes that had not be listed before • Review 10 red genes that had not previously been reviewed, 4/10 were reclassified as green • Review the remaining 145 red genes that had not previously been reviewed (shared between reviewers EM, RF, LD, AT, HB, ON & SL), resulting in 60 green, 11 amber, 70 red, 4 I don’t know reviews) • Reviewed genes from PMID: 24816252 as a publication to genes found in the Inborn error or metabolism Genes metabolomics GWAS paper (figure 5). 2 new genes added
Set Mode of Inheritance, Added New Source
Sarah Leigh (Genomics England Curator)COQ4 was added to Undiagnosed metabolic disorderspanel. Source: Expert Review Green Model of inheritance for gene COQ4 was set to BIALLELIC, autosomal or pseudoautosomal
Added New Source
Sarah Leigh (Genomics England Curator)COQ4 was added to Undiagnosed metabolic disorderspanel. Sources: Literature
Created
Sarah Leigh (Genomics England Curator)COQ4 was created by sleigh