ELOVL fatty acid elongase 4
| UniProt | Protein Name |
|---|---|
| Q9GZR5 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| fatty acid biosynthetic process | ||
| unsaturated fatty acid biosynthetic process | ||
| detection of visible light | ||
| fatty acid elongation, saturated fatty acid | ||
| fatty acid elongation, saturated fatty acid |
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum | ||
| endoplasmic reticulum membrane | ||
| endoplasmic reticulum membrane |
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| G protein-coupled photoreceptor activity | ||
| fatty acid elongase activity | ||
| fatty acid elongase activity |
| InterPro |
|---|
| ELO family |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050981 | spinocerebellar ataxia type 34 | |
| DOID:2566 | corneal dystrophy |
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000023 | Inguinal hernia |
| HP:0000230 | Gingivitis |
| HP:0000252 | Microcephaly |
| HP:0000324 | Facial asymmetry |
| HP:0000486 | Strabismus |
| HP:0000493 | Abnormal foveal morphology |
| HP:0000505 | Visual impairment |
| HP:0000551 | Color vision defect |
| Disease ID | Disease Name |
|---|---|
| OMIM:600110 |
|
| ORPHA:827 |
|
| OMIM:614457 |
|
| ORPHA:1955 |
|
| OMIM:133190 |
|
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 6785 | Xenbase:XB-GENE-5892987 | ||
| 12686 | SGD:S000004364 | ||
| 60481 | SGD:S000004364 | ||
| 64834 | SGD:S000004364 | ||
| 79993 | SGD:S000004364 | ||
| 83603 | Xenbase:XB-GENE-5892987 | MOUSE61150 | |
| 170439 | SGD:S000004364 | ||
| 171402 | SGD:S000004364 | ||
| 315851 | RATNO41181 | ||
| 393769 | DANRE11209 |
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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: August 4, 2025