UniProt | Protein Name |
---|---|
P35475 |
|
GO Term | Evidence Code | PMID |
---|---|---|
dermatan sulfate catabolic process | ||
heparin catabolic process | ||
glycosaminoglycan catabolic process | ||
disaccharide metabolic process | ||
heparan sulfate proteoglycan catabolic process |
GO Term | Evidence Code | PMID |
---|---|---|
lysosomal lumen | ||
extracellular exosome |
GO Term | Evidence Code | PMID |
---|---|---|
L-iduronidase activity | ||
signaling receptor binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050949 | autosomal recessive hypophosphatemic rickets | |
DOID:0060215 | Balo concentric sclerosis | |
DOID:0060222 | Scheie syndrome | |
DOID:0060249 | scoliosis | |
DOID:0060320 | inguinal hernia | |
DOID:0060357 | chylomicron retention disease | |
DOID:0060891 | Parkinson's disease 19A | |
DOID:0060895 | Parkinson's disease 4 | |
DOID:0060896 | Parkinson's disease 23 | |
DOID:0080001 | bone disease |
HPO ID | HPO Term |
---|---|
HP:0000455 | Broad nasal tip |
HP:0000463 | Anteverted nares |
HP:0000470 | Short neck |
HP:0000488 | Retinopathy |
HP:0000501 | Glaucoma |
HP:0000546 | Retinal degeneration |
HP:0000574 | Thick eyebrow |
HP:0000691 | Microdontia |
HP:0000716 | Depression |
HP:0000772 | Abnormal rib morphology |
Disease ID | Disease Name |
---|---|
OMIM:607016 |
|
ORPHA:93473 |
|
ORPHA:93476 |
|
OMIM:607014 |
|
OMIM:607015 |
|
ORPHA:93474 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
105483817 | MACNE34349 | ||
101021298 | PAPAN26594 | ||
105532697 | MANLE19436 | ||
101130097 | GORGO31180 | ||
461056 | PANTR33112 | ||
100458752 | PONAB28543 | ||
100505382 | CANLF12321 | ||
101095896 | FELCA10395 | ||
122218705 | PANLE27245 | ||
101320168 | TURTR01444 |
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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