UniProt | Protein Name |
---|---|
Q9C0K1 |
|
GO Term | Evidence Code | PMID |
---|---|---|
regulation of membrane potential | ||
cartilage homeostasis | ||
cadmium ion transmembrane transport | ||
extracellular matrix organization | ||
negative regulation of canonical NF-kappaB signal transduction |
GO Term | Evidence Code | PMID |
---|---|---|
plasma membrane | ||
lysosomal membrane | ||
apical plasma membrane | ||
organelle membrane | ||
basolateral plasma membrane |
GO Term | Evidence Code | PMID |
---|---|---|
monoatomic cation:bicarbonate symporter activity | ||
zinc:bicarbonate symporter activity | ||
zinc ion transmembrane transporter activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0040085 | bacterial sepsis | |
DOID:0050570 | congenital disorder of glycosylation type I | |
DOID:0050589 | inflammatory bowel disease | |
DOID:0050635 | alternating hemiplegia of childhood | |
DOID:0050741 | alcohol dependence | |
DOID:0050742 | nicotine dependence | |
DOID:0050835 | generalized dystonia | |
DOID:0050841 | focal hand dystonia | |
DOID:0060192 | Crohn's colitis | |
DOID:0060224 | atrial fibrillation |
HPO ID | HPO Term |
---|---|
HP:0001252 | Hypotonia |
HP:0001263 | Global developmental delay |
HP:0001272 | Cerebellar atrophy |
HP:0001332 | Dystonia |
HP:0001347 | Hyperreflexia |
HP:0001363 | Craniosynostosis |
HP:0001382 | Joint hypermobility |
HP:0001392 | Abnormality of the liver |
HP:0001531 | Failure to thrive in infancy |
HP:0002059 | Cerebral atrophy |
Disease ID | Disease Name |
---|---|
ORPHA:468699 |
|
OMIM:616721 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
105991224 | DIPOR11404 | ||
67547 | MGI:1914797 | MOUSE38019 | |
295455 | RGD:1308236 | RATNO25375 | |
101576991 | OCTDE22042 | ||
101870221 | MELUD07378 | ||
100014598 | MONDO26514 | ||
102457379 | PELSI08164 | ||
100555224 | ANOCA15250 | ||
107096797 | CYPVA22083 | ||
114036739 | VOMUR23906 |
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