UniProt | Protein Name |
---|---|
O15121 |
|
GO Term | Evidence Code | PMID |
---|---|---|
myelin maintenance | ||
unsaturated fatty acid biosynthetic process |
|
|
ceramide biosynthetic process | ||
sphingolipid biosynthetic process |
|
GO Term | Evidence Code | PMID |
---|---|---|
endoplasmic reticulum |
|
|
endoplasmic reticulum membrane |
|
|
mitochondrial membrane | ||
plasma membrane |
|
|
membrane |
|
GO Term | Evidence Code | PMID |
---|---|---|
electron transfer activity |
|
|
retinol isomerase activity | ||
protein binding | ||
sphingolipid delta-4 desaturase activity |
DO ID | Disease Name | Source |
---|---|---|
DOID:114 | heart disease | |
DOID:11504 | autonomic neuropathy | |
DOID:11771 | spontaneous ocular nystagmus | |
DOID:11832 | visual epilepsy | |
DOID:11847 | coronary thrombosis | |
DOID:11870 | Pick's disease | |
DOID:11963 | esophagitis | |
DOID:12139 | dysthymic disorder | |
DOID:12361 | Graves' disease | |
DOID:12697 | locked-in syndrome |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000639 | Nystagmus |
HP:0000750 | Delayed speech and language development |
HP:0000762 | Decreased nerve conduction velocity |
HP:0001250 | Seizure |
HP:0001257 | Spasticity |
HP:0001260 | Dysarthria |
HP:0001263 | Global developmental delay |
HP:0001272 | Cerebellar atrophy |
HP:0001310 | Dysmetria |
Disease ID | Disease Name |
---|---|
OMIM:618404 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
173327 | WB:WBGene00013197 | ||
177548 | WB:WBGene00017996 | ||
33836 | FB:FBgn0001941 | ||
100178733 | CIOIN08988 | ||
103181614 | CALMI23214 | ||
102357565 | LATCH04254 | ||
327075 | ZFIN:ZDB-GENE-030131-5283 | DANRE04934 | |
103035033 | ASTMX08458 | ||
108260864 | ICTPU23865 | ||
113585484 | ELEEL36057 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024