UniProt | Protein Name |
---|---|
O15056 |
|
B4DG94 |
|
A0A1W2PR85 |
|
GO Term | Evidence Code | PMID |
---|---|---|
membrane organization |
|
|
phosphatidylinositol-3-phosphate biosynthetic process | ||
phosphatidylinositol biosynthetic process |
|
|
synaptic vesicle endocytosis | ||
phosphatidylinositol dephosphorylation |
GO Term | Evidence Code | PMID |
---|---|---|
cytoskeleton | ||
cytosol |
|
|
presynapse | ||
plasma membrane | ||
cell projection |
GO Term | Evidence Code | PMID |
---|---|---|
phosphatidylinositol-3-phosphate phosphatase activity |
|
|
phosphatidylinositol-3,5-bisphosphate 5-phosphatase activity |
|
|
phosphatidylinositol-4,5-bisphosphate 5-phosphatase activity | ||
phosphatidylinositol-3,5-bisphosphate 3-phosphatase activity |
|
|
PDZ domain binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050557 | congenital muscular dystrophy | |
DOID:0050777 | Joubert syndrome | |
DOID:0060255 | rippling muscle disease 2 | |
DOID:0060894 | early-onset Parkinson's disease | |
DOID:0070247 | autosomal dominant Emery-Dreifuss muscular dystrophy 2 | |
DOID:0080092 | myofibrillar myopathy 1 | |
DOID:0080094 | myofibrillar myopathy 3 | |
DOID:0110273 | autosomal dominant limb-girdle muscular dystrophy | |
DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | |
DOID:0110275 | autosomal recessive limb-girdle muscular dystrophy type 2A |
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
178284 | WB:WBGene00006763 | ||
37517 | FB:FBgn0034691 | ||
108716710 | Xenbase:XB-GENE-6487422 | ||
100216051 | Xenbase:XB-GENE-980087 | ||
101946228 | CHRPI34239 | ||
109320087 | CROPO07524 | ||
113439266 | PSETE10831 | ||
103820593 | SERCA17097 | ||
100074182 | ORNAN16294 | ||
100920906 | SARHA04521 |
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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