UniProt | Protein Name |
---|---|
Q9NYP7 |
|
B3KWH9 |
|
A0A0A0MTI6 |
|
GO Term | Evidence Code | PMID |
---|---|---|
fatty acid elongation, monounsaturated fatty acid | ||
positive regulation of fatty acid biosynthetic process | ||
unsaturated fatty acid biosynthetic process | ||
alpha-linolenic acid metabolic process |
|
|
very long-chain fatty acid biosynthetic process |
GO Term | Evidence Code | PMID |
---|---|---|
endoplasmic reticulum | ||
dendrite | ||
neuronal cell body | ||
endoplasmic reticulum membrane | ||
membrane |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:4195 | hyperglycemia | |
DOID:0050753 | cerebellar ataxia | |
DOID:0050882 | spinocerebellar ataxia type 5 | |
DOID:0050954 | spinocerebellar ataxia type 1 | |
DOID:0050955 | spinocerebellar ataxia type 2 | |
DOID:0050956 | spinocerebellar ataxia type 6 | |
DOID:0050958 | spinocerebellar ataxia type 7 | |
DOID:0050985 | spinocerebellar ataxia type 38 | |
DOID:0060319 | cardiac arrest | |
DOID:0080199 | colorectal carcinoma |
HPO ID | HPO Term |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000514 | Slow saccadic eye movements |
HP:0000639 | Nystagmus |
HP:0000708 | Atypical behavior |
HP:0001251 | Ataxia |
HP:0001260 | Dysarthria |
HP:0001272 | Cerebellar atrophy |
HP:0001336 | Myoclonus |
HP:0001337 | Tremor |
HP:0002066 | Gait ataxia |
Disease ID | Disease Name |
---|---|
ORPHA:423296 |
|
OMIM:615957 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
610377 | CANLF02861 | ||
112914072 | VULVU05565 | ||
123795635 | URSAM20527 | ||
100465764 | AILME09000 | ||
101086147 | FELCA12103 | ||
122220032 | PANLE15677 | ||
118903606 | BALMU25532 | ||
100669438 | LOXAF20853 | ||
100069400 | HORSE19606 | ||
100171403 | PIGXX31763 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024