ATP binding cassette subfamily D member 3
| UniProt | Protein Name |
|---|---|
| P28288 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| very long-chain fatty acid metabolic process |
|
|
| fatty acid biosynthetic process |
|
|
| fatty acid beta-oxidation |
|
|
| fatty acid beta-oxidation |
|
|
| fatty acid beta-oxidation |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrion |
|
|
| peroxisome |
|
|
| peroxisome |
|
|
| peroxisomal membrane |
|
|
| peroxisomal membrane |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| long-chain fatty acid transmembrane transporter activity |
|
|
| long-chain fatty acid transmembrane transporter activity |
|
|
| long-chain fatty acid transmembrane transporter activity |
|
|
| protein binding |
|
|
| ATP binding |
|
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:905 | Zellweger syndrome | |
| DOID:0111066 | congenital bile acid synthesis defect 5 |
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000952 | Jaundice |
| HP:0001395 | Hepatic fibrosis |
| HP:0001399 | Hepatic failure |
| HP:0001409 | Portal hypertension |
| HP:0001744 | Splenomegaly |
| HP:0001891 | Iron deficiency anemia |
| HP:0002240 | Hepatomegaly |
| HP:0002904 | Hyperbilirubinemia |
| HP:0002910 | Elevated circulating hepatic transaminase concentration |
| Disease ID | Disease Name |
|---|---|
| OMIM:616278 |
|
| Species | Gene ID | Alliance of Genome Resources |
|---|---|---|
| 855956 | SGD:S000006068 | |
| 19299 | MGI:1349216 | |
| 25270 | RGD:2007 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: April 6, 2026