| IPI00815688 - GCDH, GLUTARYL COA DEHYDROGENASE (FRAGMENT). | |
|---|---|
| Uniprot Accession: Q36741 | |
| Uniprot ID: Q36741_HUMAN | |
| Mapping: Chr 19, 12862974 - 12871782 | |
| Entrez Gene: 2639 | |
| Entrez MapView: |
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| +All IPI Database Cross References | |
| IPI records in this ortholog cluster (Cluster: MGI_ORTHOLOGY_13907) |
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| Rat: Gcdh_predicted, SIMILAR TO GLUTARYL-COA DEHYDROGENASE, MITOCHONDRIAL PRECURSOR. |
| Mouse: Gcdh, GLUTARYL-COA DEHYDROGENASE, MITOCHONDRIAL PRECURSOR. |
| Mouse: Gcdh, GLUTARYL-COENZYME A DEHYDROGENASE. |
| Human: GCDH, ISOFORM LONG OF GLUTARYL-COA DEHYDROGENASE, MITOCHONDRIAL PRECURSOR. |
| Human: GCDH, ISOFORM SHORT OF GLUTARYL-COA DEHYDROGENASE, MITOCHONDRIAL PRECURSOR. |
| Human: GCDH, GLUTARYL COA DEHYDROGENASE (FRAGMENT). |
| GO Term | Aspect | Human | Mouse | Rat |
|---|---|---|---|---|
| mitochondrial inner membrane | C | IDA | ISS | |
| mitochondrion | C | IEA | IDA | ISS ISS IDA |
| acyl-CoA dehydrogenase activity | F | IEA | IEA | |
| oxidoreductase activity | F | IEA | ||
| acyl-CoA binding | F | IDA | ||
| transcription factor activity | F | RCA | ISS | |
| oxidoreductase activity, acting on the CH-CH group of donors | F | IEA | ||
| FAD binding | F | IEA | IDA IEA | |
| glutaryl-CoA dehydrogenase activity | F | IEA | ISS IDA IDA | |
| fatty acid oxidation | P | IDA | ||
| electron transport | P | IEA | IEA | |
| regulation of transcription, DNA-dependent | P | RCA | ISS | |
| metabolic process | P | IEA | IEA | |
| acyl-CoA metabolic process | P | IDA | ||
| acyl-CoA biosynthetic process | P | IDA |
| GO Graph Color Key: | Rat | Mouse | Human | Rat & Mouse | Mouse & Human | Rat & Human | Rat, Mouse & Human |
SVG image
| GO Graph Color Key: | Rat | Mouse | Human | Rat & Mouse | Mouse & Human | Rat & Human | Rat, Mouse & Human |
SVG image
| GO Graph Color Key: | Rat | Mouse | Human | Rat & Mouse | Mouse & Human | Rat & Human | Rat, Mouse & Human |
SVG image
| MP Term | Aspect | Human | Mouse | Rat |
|---|---|---|---|---|
| behavior/neurological phenotype | MP | Un | ||
| homeostasis/metabolism phenotype | MP | Un | ||
| renal/urinary system phenotype | MP | Un | ||
| nervous system phenotype | MP | Un |
| DO Term | Aspect | Human | Mouse | Rat |
|---|---|---|---|---|
| Brain Diseases, Metabolic, Inborn | D | ISS |
| KEGG Pathway | Human | Mouse | Rat |
|---|---|---|---|
| Fatty acid metabolism (00071) | Present in KEGG pathway | Present in KEGG pathway | Not present in KEGG pathway |
| Lysine degradation (00310) | Present in KEGG pathway | Present in KEGG pathway | Not present in KEGG pathway |
| Tryptophan metabolism (00380) | Present in KEGG pathway | Present in KEGG pathway | Not present in KEGG pathway |
| Benzoate degradation via CoA ligation (00632) | Present in KEGG pathway | Present in KEGG pathway | Not present in KEGG pathway |