UniProt | Protein Name |
---|---|
Q9BT40 |
|
GO Term | Evidence Code | PMID |
---|---|---|
negative regulation of protein kinase activity | ||
negative regulation of peptidyl-serine phosphorylation | ||
actin cytoskeleton organization |
|
|
regulation of glycogen biosynthetic process | ||
G protein-coupled receptor signaling pathway |
GO Term | Evidence Code | PMID |
---|---|---|
phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase activity | ||
inositol trisphosphate phosphatase activity | ||
phosphatidylinositol trisphosphate phosphatase activity | ||
inositol bisphosphate phosphatase activity | ||
phosphatidylinositol phosphate 5-phosphatase activity |
DO ID | Disease Name | Source |
---|---|---|
DOID:83 | cataract | |
DOID:870 | neuropathy | |
DOID:8923 | skin melanoma | |
DOID:8927 | learning disability | |
DOID:9277 | primary cerebellar degeneration | |
DOID:9306 | mechanical strabismus | |
DOID:9521 | Laron syndrome | |
DOID:9649 | congenital nystagmus | |
DOID:9650 | pathologic nystagmus | |
DOID:9837 | hypertropia |
HPO ID | HPO Term |
---|---|
HP:0003306 | Spinal rigidity |
HP:0003307 | Hyperlordosis |
HP:0003391 | Gowers sign |
HP:0003510 | Severe short stature |
HP:0003552 | Muscle stiffness |
HP:0003560 | Muscular dystrophy |
HP:0003577 | Congenital onset |
HP:0003593 | Infantile onset |
HP:0003676 | Progressive |
HP:0003701 | Proximal muscle weakness |
Disease ID | Disease Name |
---|---|
OMIM:617404 |
|
ORPHA:559 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
103111156 | ERIEU13613 | ||
100399558 | CALJA35819 | ||
100404632 | CALJA35819 | ||
105584255 | CERAT17249 | ||
721222 | MACMU14327 | ||
105471610 | MACNE31715 | ||
101011974 | PAPAN14773 | ||
105553494 | MANLE01908 | ||
101124081 | GORGO13519 | ||
100976910 | PANPA15978 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024