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:12802 | mucopolysaccharidosis I | |
DOID:12803 | Sly syndrome | |
DOID:12804 | mucopolysaccharidosis IV | |
DOID:12858 | Huntington's disease | |
DOID:12932 | endomyocardial fibrosis | |
DOID:12987 | agranulocytosis | |
DOID:13121 | deficiency anemia | |
DOID:1319 | brain cancer | |
DOID:14159 | obstructive hydrocephalus | |
DOID:1432 | blindness |
HPO ID | HPO Term |
---|---|
HP:0001252 | Hypotonia |
HP:0001263 | Global developmental delay |
HP:0001371 | Flexion contracture |
HP:0001376 | Limitation of joint mobility |
HP:0001387 | Joint stiffness |
HP:0001433 | Hepatosplenomegaly |
HP:0001488 | Bilateral ptosis |
HP:0001510 | Growth delay |
HP:0001522 | Death in infancy |
HP:0001537 | Umbilical hernia |
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 |
---|---|---|---|
100596160 | NOMLE19147 | ||
107572256 | SINGR98776 | ||
111569438 | AMPOC00332 | ||
116823765 | CHEAB07419 | ||
109511648 | HIPCM06971 | ||
115049250 | ECHNA20531 | ||
115398456 | SALFA07905 | ||
103398091 | CYNSE32493 | ||
103741112 | NANGA15171 | ||
115619883 | STRHB08011 |
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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