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:11984 | hypertrophic cardiomyopathy | |
DOID:12139 | dysthymic disorder | |
DOID:1222 | cartilage disease | |
DOID:1227 | neutropenia | |
DOID:12603 | acute leukemia | |
DOID:12721 | multiple epiphyseal dysplasia | |
DOID:12798 | mucopolysaccharidosis | |
DOID:12799 | mucopolysaccharidosis II | |
DOID:12800 | mucopolysaccharidosis VI | |
DOID:12801 | mucopolysaccharidosis III |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000023 | Inguinal hernia |
HP:0000154 | Wide mouth |
HP:0000158 | Macroglossia |
HP:0000212 | Gingival overgrowth |
HP:0000232 | Everted lower lip vermilion |
HP:0000238 | Hydrocephalus |
HP:0000256 | Macrocephaly |
HP:0000268 | Dolichocephaly |
HP:0000280 | Coarse facial features |
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 |
---|---|---|---|
115581344 | SPAAU13085 | ||
446866 | Xenbase:XB-GENE-986808 | ||
101949799 | CHRPI22318 | ||
109323410 | CROPO12981 | ||
113444136 | PSETE16776 | ||
103821276 | SERCA17260 | ||
100083541 | ORNAN30573 | ||
100896352 | CALJA29278 | ||
105585503 | CERAT31756 | ||
106998222 | MACMU36031 |
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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