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:0000007 | Autosomal recessive inheritance |
HP:0000023 | Inguinal hernia |
HP:0000158 | Macroglossia |
HP:0000238 | Hydrocephalus |
HP:0000256 | Macrocephaly |
HP:0000268 | Dolichocephaly |
HP:0000280 | Coarse facial features |
HP:0000365 | Hearing impairment |
HP:0000501 | Glaucoma |
HP:0000670 | Carious teeth |
Disease ID | Disease Name |
---|---|
OMIM:253200 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
102025379 | CHILA07990 | ||
105723871 | AOTNA06964 | ||
111239020 | SERDU28323 | ||
108411980 | PYGNA32406 | ||
101971329 | ICTTR04467 | ||
101596481 | JACJA02725 | ||
118301042 | SCOMX24806 | ||
102418809 | MYOLU00228 | ||
117025064 | RHIFE13103 | ||
100228383 | TAEGU31762 |
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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