UniProt | Protein Name |
---|---|
Q16394 |
|
GO Term | Evidence Code | PMID |
---|---|---|
sodium ion homeostasis | ||
heparan sulfate proteoglycan biosynthetic process, polysaccharide chain biosynthetic process | ||
olfactory bulb development | ||
cell adhesion mediated by integrin | ||
lymphocyte migration into lymphoid organs |
GO Term | Evidence Code | PMID |
---|---|---|
endoplasmic reticulum | ||
endoplasmic reticulum membrane | ||
synapse | ||
catalytic complex | ||
Golgi apparatus |
GO Term | Evidence Code | PMID |
---|---|---|
heparan sulfate N-acetylglucosaminyltransferase activity | ||
protein homodimerization activity | ||
glucuronosyl-N-acetylglucosaminyl-proteoglycan 4-alpha-N-acetylglucosaminyltransferase activity | ||
metal ion binding | ||
acetylglucosaminyltransferase activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Species | Protein | mRNA |
---|---|---|
Rattus norvegicus | XP_216920 | XM_216920 |
Drosophila melanogaster | NP_477231 | NM_057883 |
Caenorhabditis elegans | NP_502180 | NM_069779 |
Mus musculus | NP_034292 | NM_010162 |
DO ID | Disease Name | Source |
---|---|---|
DOID:0050561 | Lennox-Gastaut syndrome | |
DOID:0060041 | autism spectrum disorder | |
DOID:0060221 | Maffucci syndrome | |
DOID:0060249 | scoliosis | |
DOID:0060262 | gallbladder disease | |
DOID:0060467 | humeroradial synostosis | |
DOID:0060672 | Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | |
DOID:0060847 | Leri-Weill dyschondrosteosis | |
DOID:0080001 | bone disease | |
DOID:0080144 | childhood acute lymphocytic leukemia |
HPO ID | HPO Term |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000010 | Recurrent urinary tract infections |
HP:0000016 | Urinary retention |
HP:0000076 | Vesicoureteral reflux |
HP:0000164 | Abnormality of the dentition |
HP:0000174 | Abnormal palate morphology |
HP:0000219 | Thin upper lip vermilion |
HP:0000252 | Microcephaly |
HP:0000343 | Long philtrum |
HP:0000368 | Low-set, posteriorly rotated ears |
Disease ID | Disease Name |
---|---|
ORPHA:321 |
|
OMIM:215300 |
|
OMIM:133700 |
|
ORPHA:502 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
102441376 | MYOLU02711 | ||
117033795 | RHIFE04954 | ||
100227900 | TAEGU17803 | ||
108536176 | RHIBE13599 | ||
104658897 | RHIRO29799 | ||
100597702 | NOMLE11703 | ||
113153482 | ANATE05041 | ||
107592940 | SINGR37448 | ||
115050656 | ECHNA19033 | ||
115380876 | SALFA49393 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
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