UniProt | Protein Name |
---|---|
O60931 |
|
I3L4A9 |
|
A0A0S2Z3K3 |
|
A0A0S2Z3I9 |
|
GO Term | Evidence Code | PMID |
---|---|---|
transmembrane transport |
|
|
visual learning | ||
positive regulation of TORC1 signaling | ||
melanin biosynthetic process | ||
negative regulation of apoptotic process |
GO Term | Evidence Code | PMID |
---|---|---|
intracellular membrane-bounded organelle | ||
melanosome | ||
plasma membrane | ||
lysosomal membrane | ||
early endosome |
DO ID | Disease Name | Source |
---|---|---|
DOID:11105 | fundus albipunctatus | |
DOID:11155 | hypohidrosis | |
DOID:11156 | anhidrosis | |
DOID:11541 | recurrent corneal erosion | |
DOID:11719 | oculopharyngeal muscular dystrophy | |
DOID:11720 | distal myopathy | |
DOID:11724 | limb-girdle muscular dystrophy | |
DOID:11727 | facioscapulohumeral muscular dystrophy | |
DOID:11870 | Pick's disease | |
DOID:1222 | cartilage disease |
HPO ID | HPO Term |
---|---|
HP:0001508 | Failure to thrive |
HP:0001510 | Growth delay |
HP:0001531 | Failure to thrive in infancy |
HP:0001738 | Exocrine pancreatic insufficiency |
HP:0001744 | Splenomegaly |
HP:0001824 | Weight loss |
HP:0001941 | Acidosis |
HP:0001942 | Metabolic acidosis |
HP:0001944 | Dehydration |
HP:0001959 | Polydipsia |
Disease ID | Disease Name |
---|---|
OMIM:219800 |
|
ORPHA:411629 |
|
OMIM:219900 |
|
ORPHA:411641 |
|
ORPHA:411634 |
|
OMIM:219750 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100669881 | LOXAF07846 | ||
100060554 | HORSE03110 | ||
100515235 | PIGXX03131 | ||
613527 | BOVIN12569 | ||
102187709 | CAPHI10245 | ||
101122533 | SHEEP02647 | ||
105983465 | DIPOR08657 | ||
83429 | MGI:1932872 | MOUSE07194 | |
287478 | RGD:1308466 | RATNO00724 | |
101721174 | HETGA14366 |
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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