WormBase Tree Display for Gene: HGNC:3247
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| HGNC:3247 | Identity | Name | CGC_name | Ehhadh | Inferred_automatically | AGR_import |
|---|---|---|---|---|---|---|
| Other_name (18) | ||||||
| Public_name | Ehhadh | |||||
| DB_info | Database | HGNC | id | 3247 | ||
| AGR | cURI | HGNC:3247 | ||||
| EnsEMBL | ENSEMBL_geneID | ENSG00000113790 | ||||
| UniProt | UniProt_AC | Q08426 | ||||
| OMIM | gene | 607037 | ||||
| DO | id | DOID:0080759 | ||||
| Species | Homo sapiens | |||||
| Status | Live | |||||
| Gene_info | Biotype | SO:0001217 | ||||
| Ortholog | WBGene00001157 | Caenorhabditis elegans | From_analysis | EnsEMBL-Compara | ||
| Hieranoid | ||||||
| Panther | ||||||
| PhylomeDB | ||||||
| WBGene00001158 | Caenorhabditis elegans | From_analysis | EnsEMBL-Compara | |||
| Hieranoid | ||||||
| Panther | ||||||
| PhylomeDB | ||||||
| Structured_description | Automated_description | 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] | Inferred_automatically | AGR_import |
