EHHADH (Gene)

Synonyms:ECHD, EHHADH, ENTREZ:1962, FRTS3, HGNC:3247, L-PBE, LBFP, LBP, MFE1, MIM:607037, NM_001166415, NM_001966, NP_001159887, NP_001957, PBFE, XM_006713525, XP_006713588, enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase
Omim:OMIM:607037
Id:e116e184-f75b-5fc6-8ba5-2c75bb70fbdf
Hgnc:HGNC:3247
Entrez:1962
Description:enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase
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]

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Data Distillery
CFDE DD-Knowledge Graph

The CFDE Data Distillery Knowledge Graph contains entities and relationships across the CFDE. View EHHADH's neighborhood in the knowledge graph.

Playbook Workflow Builder
Playbook Workflow Builder: Gene-Centric Workflow

View Gene-Centric information about the gene from a pre-built PWB workflow. View the workflow with EHHADH.

Gene Partnership Appyter
CFDE Gene-Centric Appyter

The CFDE Gene Centric Appyter Resolves and Displays Gene-Centric information from CFDE APIs. Execute the Appyter using EHHADH.

Gene and Drug Landing Page Aggregator
GDLPA Landing Pages Links

The Gene and Drug Landing Page Aggregator (GDLPA) finds links to primary and secondary source information from CFDE and other resources. Discover landing pages for EHHADH.

Playbook Workflow Builder
Playbook Workflow Builder

The Playbook Workflow Builder helps you interactively construct workflows leveraging CFDE APIs without code. Start a new workflow with EHHADH.

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