GO Term | Evidence Code | PMID |
---|---|---|
regulation of epithelial cell migration | ||
response to nutrient | ||
lysosomal transport |
|
|
lysosome organization |
|
|
positive regulation of neuron projection development |
GO Term | Evidence Code | PMID |
---|---|---|
endoplasmic reticulum lumen |
|
|
extracellular region |
|
|
cell surface | ||
lysosomal lumen |
|
|
ficolin-1-rich granule lumen |
|
GO Term | Evidence Code | PMID |
---|---|---|
N-acetylgalactosamine-4-sulfatase activity | ||
metal ion binding | ||
arylsulfatase activity |
|
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050700 | cardiomyopathy | |
DOID:0060215 | Balo concentric sclerosis | |
DOID:0060222 | Scheie syndrome | |
DOID:0060320 | inguinal hernia | |
DOID:0060321 | umbilical hernia | |
DOID:0060327 | omphalocele | |
DOID:0060357 | chylomicron retention disease | |
DOID:0080199 | colorectal carcinoma | |
DOID:0111390 | mucopolysaccharidosis Ih | |
DOID:0111391 | mucopolysaccharidosis IVA |
HPO ID | HPO Term |
---|---|
HP:0001371 | Flexion contracture |
HP:0001385 | Hip dysplasia |
HP:0001387 | Joint stiffness |
HP:0001537 | Umbilical hernia |
HP:0001638 | Cardiomyopathy |
HP:0001653 | Mitral regurgitation |
HP:0001718 | Mitral stenosis |
HP:0001744 | Splenomegaly |
HP:0002090 | Pneumonia |
HP:0002091 | Restrictive ventilatory defect |
Disease ID | Disease Name |
---|---|
OMIM:253200 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
101879959 | MELUD16362 | ||
100032622 | MONDO18033 | ||
102445150 | PELSI13307 | ||
100564703 | ANOCA02102 | ||
107093772 | CYPVA18398 | ||
113899711 | BOBOX21474 | ||
100944911 | OTOGA15270 | ||
112162825 | ORYME18556 | ||
101061832 | TAKRU45194 | ||
102799236 | NEOBR16958 |
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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