UniProt | Protein Name |
---|---|
P16885 |
|
GO Term | Evidence Code | PMID |
---|---|---|
positive regulation of I-kappaB phosphorylation | ||
cellular response to calcium ion | ||
B cell differentiation | ||
positive regulation of MAPK cascade | ||
negative regulation of programmed cell death |
GO Term | Evidence Code | PMID |
---|---|---|
perinuclear region of cytoplasm | ||
membrane raft | ||
extracellular exosome |
GO Term | Evidence Code | PMID |
---|---|---|
phospholipase C activity |
|
|
scaffold protein binding | ||
protein kinase binding | ||
protein tyrosine kinase binding | ||
phosphotyrosine residue binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0060901 | lymphoplasmacytic lymphoma | |
DOID:0070129 | autosomal recessive cutis laxa type IID | |
DOID:0070130 | autosomal dominant cutis laxa 1 | |
DOID:0070131 | autosomal dominant cutis laxa 3 | |
DOID:0070132 | autosomal recessive cutis laxa type IIIA | |
DOID:0070133 | autosomal recessive cutis laxa type IB | |
DOID:0070134 | autosomal recessive cutis laxa type IIA | |
DOID:0070135 | autosomal recessive cutis laxa type IA | |
DOID:0070136 | autosomal dominant cutis laxa 2 | |
DOID:0070137 | autosomal recessive cutis laxa type IIB |
HPO ID | HPO Term |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000403 | Recurrent otitis media |
HP:0000518 | Cataract |
HP:0000872 | Hashimoto thyroiditis |
HP:0000989 | Pruritus |
HP:0001045 | Vitiligo |
HP:0002099 | Asthma |
HP:0002720 | Decreased circulating IgA level |
HP:0002829 | Arthralgia |
HP:0002850 | Decreased circulating total IgM |
Disease ID | Disease Name |
---|---|
OMIM:614878 |
|
OMIM:614468 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
116449881 | CORMO02267 | ||
103267377 | CARSF01195 | ||
115619893 | STRHB07368 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024