ATP binding cassette subfamily D member 1
| UniProt | Protein Name |
|---|---|
| P33897 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| very long-chain fatty acid metabolic process | ||
| regulation of oxidative phosphorylation | ||
| fatty acid beta-oxidation | ||
| fatty acid beta-oxidation | ||
| fatty acid beta-oxidation |
| GO Term | Evidence Code | PMID |
|---|---|---|
| cytoplasm | ||
| lysosomal membrane | ||
| peroxisome | ||
| peroxisomal membrane | ||
| peroxisomal membrane |
| GO Term | Evidence Code | PMID |
|---|---|---|
| long-chain fatty acid transporter activity | ||
| long-chain fatty acid transporter activity | ||
| long-chain fatty acid transporter activity | ||
| long-chain fatty acid transporter activity | ||
| protein binding |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:10588 | adrenoleukodystrophy |
| HPO ID | HPO Term |
|---|---|
| HP:0012501 | Abnormal brainstem white matter morphology |
| HP:0012534 | Dysesthesia |
| HP:0012719 | Functional abnormality of the gastrointestinal tract |
| HP:0100031 | Neoplasm of the thyroid gland |
| HP:0100291 | Delayed somatosensory central conduction time |
| HP:0100502 | Decreased circulating vitamin B12 concentration |
| HP:0100543 | Cognitive impairment |
| HP:0100639 | Erectile dysfunction |
| HP:0100806 | Sepsis |
| HP:0100816 | Lip hyperpigmentation |
| Disease ID | Disease Name |
|---|---|
| ORPHA:139396 |
|
| ORPHA:139399 |
|
| ORPHA:388 |
|
| OMIM:300100 |
|
| ORPHA:369942 |
|
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: April 6, 2026