Gene ID | Gene Symbol | Description | Source |
---|---|---|---|
2720 | GLB1 | galactosidase beta 1 | |
3339 | HSPG2 | heparan sulfate proteoglycan 2 | |
3418 | IDH2 | isocitrate dehydrogenase (NADP(+)) 2 | |
3612 | IMPA1 | inositol monophosphatase 1 | |
3633 | INPP5B | inositol polyphosphate-5-phosphatase B | |
3958 | LGALS3 | galectin 3 | |
4153 | MBL2 | mannose binding lectin 2 | |
5286 | PIK3C2A | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha | |
5373 | PMM2 | phosphomannomutase 2 | |
5553 | PRG2 | proteoglycan 2, pro eosinophil major basic protein |
UniProt ID | Protein Name | Source |
---|---|---|
Q9P2X0 | Dolichol-phosphate mannosyltransferase subunit 3 | |
Q9UKY4 | Protein O-mannosyl-transferase 2 | |
Q9Y259 | Choline/ethanolamine kinase | |
Q9Y2B1 | Ribitol-5-phosphate xylosyltransferase 1 | |
Q9Y5P6 | Mannose-1-phosphate guanyltransferase beta | |
Q9Y6A1 | Protein O-mannosyl-transferase 1 |
HPO ID | HPO Term |
---|---|
HP:0002317 | Unsteady gait |
HP:0008981 | Calf muscle hypertrophy |
HP:0002515 | Waddling gait |
HP:0003551 | Difficulty climbing stairs |
HP:0001263 | Global developmental delay |
HP:0003560 | Muscular dystrophy |
HP:0000750 | Delayed speech and language development |
HP:0011463 | Childhood onset |
HP:0002355 | Difficulty walking |
HP:0000007 | Autosomal recessive inheritance |
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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