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:0001284 | Areflexia |
HP:0001288 | Gait disturbance |
HP:0001321 | Cerebellar hypoplasia |
HP:0001328 | Specific learning disability |
HP:0001385 | Hip dysplasia |
HP:0001460 | Aplasia/Hypoplasia involving the skeletal musculature |
HP:0001618 | Dysphonia |
HP:0002061 | Lower limb spasticity |
HP:0002063 | Rigidity |
HP:0002093 | Respiratory insufficiency |
Disease ID | Disease Name |
---|---|
OMIM:617404 |
|
ORPHA:559 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
101875341 | MELUD09472 | ||
100619651 | MONDO15625 | ||
102464080 | PELSI03516 | ||
103667174 | URSMA14083 | ||
113877320 | BOBOX15650 | ||
105857975 | MICMU10287 | ||
100945090 | OTOGA04234 | ||
101066042 | TAKRU03971 | ||
102020444 | CHILA18171 | ||
105714390 | AOTNA32100 |
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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