======= EHHADH ======= == Gene Information == * **Official Symbol**: EHHADH * **Official Name**: enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=1962|1962]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q08426|Q08426]] * **Interactions**: [[https://thebiogrid.org/search.php?search=EHHADH&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20EHHADH|Open PubMed]] * **OMIM**: [[https://omim.org/entry/607037|Open OMIM]] == Function Summary == * **Entrez Summary**: 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-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]. * **UniProt Summary**: N/A |3HCDH| |3HCDH N| |ECH| |dodecenoyl-CoA delta-isomerase activity| |long-chain-enoyl-CoA hydratase activity| |3-hydroxyacyl-CoA dehydrogenase activity| |enoyl-CoA hydratase activity| |fatty acid beta-oxidation using acyl-CoA oxidase| |peroxisomal matrix| |fatty acid beta-oxidation| |protein targeting to peroxisome| |protein localization to peroxisome| |establishment of protein localization to peroxisome| |peroxisomal transport| |fatty acid oxidation| |lipid oxidation| |peroxisome organization| |fatty acid catabolic process| |peroxisome| |monocarboxylic acid catabolic process| |internal protein amino acid acetylation| |protein acetylation| |protein acylation| |cellular lipid catabolic process| |lipid modification| |organic acid catabolic process| |carboxylic acid catabolic process| |lipid catabolic process| |fatty acid metabolic process| |enzyme binding| |protein targeting| |establishment of protein localization to organelle| |small molecule catabolic process| |monocarboxylic acid metabolic process| |protein localization to organelle| |carboxylic acid metabolic process| |cellular lipid metabolic process| |oxidation-reduction process| |intracellular protein transport| |oxoacid metabolic process| |organic acid metabolic process| |lipid metabolic process| |protein transport| |intracellular transport| |peptide transport| |amide transport| |cellular protein localization| |cellular macromolecule localization| |establishment of protein localization| |small molecule metabolic process| |organic substance catabolic process| |cellular catabolic process| |establishment of localization in cell| |nitrogen compound transport| \\ === CRISPR Data === No hits were found. No correlation found to any other genes in chemogenomics. Global Fraction of Cell Lines Where Essential: 0/739 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/28| |bone|0/26| |breast|0/33| |central nervous system|0/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/16| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|0/16| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/9| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/29| |uterus|0/5| == Essentiality in NALM6 == * **Essentiality Rank**: 8617 * **Expression level (log2 read counts)**: 1.43 {{:chemogenomics:nalm6 dist.png?nolink |}}