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EHHADH (enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
1962
Gene nameGene Name - the full gene name approved by the HGNC.
Enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
EHHADH
SynonymsGene synonyms aliases
ECHD, FRTS3, L-PBE, LBFP, LBP, MFE1, PBFE
ChromosomeChromosome number
3
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3q27.2
SummarySummary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-h
SNPsSNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs140527463 A>C Conflicting-interpretations-of-pathogenicity Missense variant, coding sequence variant
rs140735525 T>C Conflicting-interpretations-of-pathogenicity Missense variant, coding sequence variant
rs141355337 C>T Conflicting-interpretations-of-pathogenicity Synonymous variant, coding sequence variant
rs144464757 G>A Conflicting-interpretations-of-pathogenicity Missense variant, coding sequence variant
rs146431168 C>T Conflicting-interpretations-of-pathogenicity Coding sequence variant, missense variant
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT036469 hsa-miR-1226-3p CLASH 23622248
MIRT715150 hsa-miR-6889-3p HITS-CLIP 19536157
MIRT715149 hsa-miR-4252 HITS-CLIP 19536157
MIRT715148 hsa-miR-1254 HITS-CLIP 19536157
MIRT715147 hsa-miR-3116 HITS-CLIP 19536157
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003857 Function 3-hydroxyacyl-CoA dehydrogenase activity IBA 21873635
GO:0003857 Function 3-hydroxyacyl-CoA dehydrogenase activity IDA 15060085
GO:0003857 Function 3-hydroxyacyl-CoA dehydrogenase activity ISS
GO:0003857 Function 3-hydroxyacyl-CoA dehydrogenase activity NAS 8188243
GO:0003857 Function 3-hydroxyacyl-CoA dehydrogenase activity TAS
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID Q08426
Protein name Peroxisomal bifunctional enzyme (PBE) (PBFE) (L-bifunctional protein) (LBP) (Multifunctional enzyme 1) (MFE1) [Includes: Enoyl-CoA hydratase/3,2-trans-enoyl-CoA isomerase (EC 4.2.1.17) (EC 5.3.3.8); 3-hydroxyacyl-CoA dehydrogenase (EC 1.1.1.35)]
Protein function Peroxisomal trifunctional enzyme possessing 2-enoyl-CoA hydratase, 3-hydroxyacyl-CoA dehydrogenase, and delta 3, delta 2-enoyl-CoA isomerase activities. Catalyzes two of the four reactions of the long chain fatty acids peroxisomal beta-oxidation
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00378 ECH_1
6 215
Enoyl-CoA hydratase/isomerase
Domain
PF02737 3HCDH_N
299 476
3-hydroxyacyl-CoA dehydrogenase, NAD binding domain
Domain
PF00725 3HCDH
478 582
3-hydroxyacyl-CoA dehydrogenase, C-terminal domain
Domain
PF00725 3HCDH
619 715
3-hydroxyacyl-CoA dehydrogenase, C-terminal domain
Domain
Sequence
Sequence length 723
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.
 
KEGG
 
Reactome
  Fatty acid degradation
Valine, leucine and isoleucine degradation
Lysine degradation
Tryptophan metabolism
beta-Alanine metabolism
Propanoate metabolism
Butanoate metabolism
Metabolic pathways
Fatty acid metabolism
PPAR signaling pathway
Peroxisome
  Beta-oxidation of very long chain fatty acids
Peroxisomal protein import
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Bifunctional enzyme deficiency Bifunctional enzyme deficiency rs1554065670, rs1554065254, rs137853097, rs25640, rs775832137, rs587777443, rs775766910, rs368744809, rs863225438, rs765702241, rs1057516672, rs1057516958, rs1057516310, rs1057516750, rs969485098, rs1057516269, rs1057517118, rs1057516735, rs1057517045, rs1057516273, rs1057516859, rs755412738, rs1057517323, rs1057516936, rs1057516312, rs1057517152, rs766199971, rs758055753, rs1554066421, rs1554068136, rs1554068426, rs1554068134, rs1554068960, rs1554069610, rs1554062168, rs1276397342, rs1554064083, rs1554065671, rs1554069592, rs751646311, rs1554059509, rs1224475289, rs1231357043, rs1554062343, rs1171426785, rs1561457987, rs749532705, rs1038744864, rs1580711803
Fanconi syndrome De Toni-Debre-Fanconi Syndrome, FANCONI RENOTUBULAR SYNDROME 3, FANCONI RENOTUBULAR SYNDROME 1, Fanconi Syndrome, Adult Fanconi syndrome, Primary Fanconi renotubular syndrome rs398124646 24401050
Fanconi-bickel syndrome Fanconi-Bickel Syndrome rs121909742, rs121909743, rs121909744, rs121909745, rs1715390589, rs780067980, rs771477447, rs28928874, rs1576838294, rs121909746, rs121909747, rs1114167428, rs371977235, rs1553785033, rs769888108, rs756874949, rs1553784980, rs1553785722, rs1553786361, rs1560035336, rs1560033414, rs1447936042, rs1318756243
Prostate cancer Malignant neoplasm of prostate rs121909139, rs121909140, rs121909141, rs121909142, rs121909143, rs606231169, rs606231170, rs137852584, rs137852578, rs137852580, rs137852581, rs137852582 29610475
Unknown
Disease name Disease term dbSNP ID References
Bipolar disorder Bipolar Disorder 16380905
Dwarfism Dwarfism
Phosphate diabetes Phosphate Diabetes
Prostatic neoplasms Prostatic Neoplasms 29610475

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