UniProt | Protein Name |
---|---|
P07686 |
|
A0A024RAJ6 |
|
Q5URX0 |
|
GO Term | Evidence Code | PMID |
---|---|---|
dermatan sulfate catabolic process | ||
single fertilization | ||
myelination | ||
intracellular calcium ion homeostasis | ||
hyaluronan catabolic process |
GO Term | Evidence Code | PMID |
---|---|---|
cortical granule | ||
extracellular region | ||
azurophil granule | ||
membrane | ||
lysosomal lumen |
GO Term | Evidence Code | PMID |
---|---|---|
beta-N-acetylhexosaminidase activity | ||
N-acetyl-beta-D-galactosaminidase activity | ||
acetylglucosaminyltransferase activity | ||
protein binding | ||
identical protein binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:3211 | lysosomal storage disease | |
DOID:3320 | Tay-Sachs disease | |
DOID:3321 | GM2 gangliosidosis | |
DOID:3323 | Sandhoff disease | |
DOID:3535 | Unverricht-Lundborg syndrome | |
DOID:3612 | retinitis | |
DOID:3620 | central nervous system cancer | |
DOID:4752 | multiple system atrophy | |
DOID:4795 | GM2 gangliosidosis, AB variant | |
DOID:4873 | anterior horn cell disease |
HPO ID | HPO Term |
---|---|
HP:0000975 | Hyperhidrosis |
HP:0001250 | Seizure |
HP:0001251 | Ataxia |
HP:0001252 | Hypotonia |
HP:0001257 | Spasticity |
HP:0001260 | Dysarthria |
HP:0001268 | Mental deterioration |
HP:0001272 | Cerebellar atrophy |
HP:0001278 | Orthostatic hypotension |
HP:0001288 | Gait disturbance |
Disease ID | Disease Name |
---|---|
ORPHA:309155 |
|
OMIM:268800 |
|
ORPHA:309162 |
|
ORPHA:309169 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100438599 | PONAB29646 | ||
100465984 | AILME14836 | ||
493928 | FELCA00228 | ||
118891818 | BALMU06072 | ||
100666725 | LOXAF16808 | ||
100073289 | HORSE08996 | ||
396958 | PIGXX19251 | ||
618571 | BOVIN15770 | ||
786974 | BOVIN15771 | ||
102181720 | CAPHI12931 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024