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:0111395 | mucopolysaccharidosis type IIIA | |
DOID:10003 | sensorineural hearing loss | |
DOID:10159 | osteonecrosis | |
DOID:10283 | prostate cancer | |
DOID:10286 | prostate carcinoma | |
DOID:10581 | metachromatic leukodystrophy | |
DOID:10588 | adrenoleukodystrophy | |
DOID:10763 | hypertension | |
DOID:10825 | essential hypertension | |
DOID:10908 | hydrocephalus |
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 |
---|---|---|---|
105303556 | PTEVA09174 | ||
115051583 | ECHNA50239 | ||
115383284 | SALFA13104 | ||
113489665 | ATHCN09848 | ||
103390010 | CYNSE08351 | ||
103390011 | CYNSE08354 | ||
103390012 | CYNSE08352 | ||
105826553 | PROCO02092 | ||
109046309 | CYPCA133565 | ||
103750289 | NANGA04837 |
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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