- 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: FH Green List (high evidence)EnsemblGeneIds (GRCh38): ENSG00000091483
EnsemblGeneIds (GRCh37): ENSG00000091483
OMIM: 136850, Gene2Phenotype
FH is in 21 panels
0 reviews
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Literature
- Phenotypes
-
- Fumarase deficiency, OMIM:606812
- Disorders of the citric acid cycle
- OMIM
- 136850
- Clinvar variants
- Variants in FH
- Penetrance
- Complete
- Publications
- Panels with this gene
-
- Inherited phaeochromocytoma and paraganglioma
- Endometrial cancer pertinent cancer susceptibility
- Childhood onset dystonia, chorea or related movement disorder
- Sarcoma cancer susceptibility
- Inherited renal cancer
- Undiagnosed metabolic disorders
- Fetal hydrops
- Early onset or syndromic epilepsy
- Mitochondrial disorders
- Fumarate hydratase-related tumour syndromes
- Adult solid tumours for rare disease
- Renal cancer pertinent cancer susceptibility
- Sarcoma susceptibility
- Likely inborn error of metabolism
- Intellectual disability
- Possible mitochondrial disorder - nuclear genes
- Adult solid tumours cancer susceptibility
- Inherited phaeochromocytoma and paraganglioma excluding NF1
- Fetal anomalies
- DDG2P
- Neuroendocrine cancer pertinent cancer susceptibility
History Filter Activity
Set Phenotypes
Arina Puzriakova (Genomics England Curator)Phenotypes for gene: FH were changed from Fumarase deficiency (Disorders of the citric acid cycle); Fumarase deficiency, 606812 to Fumarase deficiency, OMIM:606812; Disorders of the citric acid cycle
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)FH was added to Undiagnosed metabolic disorderspanel. Source: Expert Review Green Model of inheritance for gene FH was set to BIALLELIC, autosomal or pseudoautosomal
Created
Sarah Leigh (Genomics England Curator)FH was created by sleigh
Added New Source
Sarah Leigh (Genomics England Curator)FH was added to Undiagnosed metabolic disorderspanel. Sources: Literature