EHHADH (enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase)
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Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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1962 |
Gene nameGene Name - the full gene name approved by the HGNC.
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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.
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EHHADH |
SynonymsGene synonyms aliases
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ECHD, FRTS3, L-PBE, LBFP, LBP, MFE1, PBFE |
ChromosomeChromosome number
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3 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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3q27.2 |
SummarySummary of gene provided in NCBI Entrez Gene.
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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.
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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 |
rs150744159 |
C>A,T |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, missense variant |
rs752275123 |
G>A |
Conflicting-interpretations-of-pathogenicity |
Coding sequence variant, synonymous variant |
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miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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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 |
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Sequence |
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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.
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Associated diseases
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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 |
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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 |
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Prostate cancer |
Malignant neoplasm of prostate |
rs121909139, rs121909140, rs121909141, rs121909142, rs121909143, rs606231169, rs606231170, rs137852584, rs137852578, rs137852580, rs137852581, rs137852582 |
29610475 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Bipolar disorder |
Bipolar Disorder |
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16380905 |
Dwarfism |
Dwarfism |
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Phosphate diabetes |
Phosphate Diabetes |
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Prostatic neoplasms |
Prostatic Neoplasms |
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29610475 |
Rickets |
Rickets |
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