Gene ID | Gene Symbol | Description | Source |
---|---|---|---|
5476 | CTSA | cathepsin A | |
6448 | SGSH | N-sulfoglucosamine sulfohydrolase | |
6677 | SPAM1 | sperm adhesion molecule 1 | |
8692 | HYAL2 | hyaluronidase 2 | |
10020 | GNE | glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | |
10724 | OGA | O-GlcNAcase | |
22901 | ARSG | arylsulfatase G | |
51172 | NAGPA | N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase | |
79158 | GNPTAB | N-acetylglucosamine-1-phosphate transferase subunits alpha and beta | |
84572 | GNPTG | N-acetylglucosamine-1-phosphate transferase subunit gamma |
UniProt ID | Protein Name | Source |
---|---|---|
O00754 | Lysosomal alpha-mannosidase | |
O43909 | Exostosin-like 3 | |
O60502 | Protein O-GlcNAcase | |
P04040 | Catalase | |
P04066 | Tissue alpha-L-fucosidase | |
P07741 | Adenine phosphoribosyltransferase | |
P08236 | Beta-glucuronidase | |
P10619 | Lysosomal protective protein | |
P15289 | Arylsulfatase A | |
P15586 | N-acetylglucosamine-6-sulfatase |
HPO ID | HPO Term |
---|---|
HP:0001260 | Dysarthria |
HP:0001263 | Global developmental delay |
HP:0001272 | Cerebellar atrophy |
HP:0001344 | Absent speech |
HP:0001348 | Brisk reflexes |
HP:0001385 | Hip dysplasia |
HP:0001387 | Joint stiffness |
HP:0001507 | Growth abnormality |
HP:0001653 | Mitral regurgitation |
HP:0001670 | Asymmetric septal hypertrophy |
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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