UniProt | Protein Name |
---|---|
Q9NRR6 |
|
GO Term | Evidence Code | PMID |
---|---|---|
biological_process | ||
negative regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction | ||
phosphatidylinositol-3-phosphate biosynthetic process | ||
phosphatidylinositol biosynthetic process |
|
|
negative regulation of translation |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:684 | hepatocellular carcinoma | |
DOID:83 | cataract | |
DOID:8501 | fundus dystrophy | |
DOID:8738 | leukoplakia of penis | |
DOID:8923 | skin melanoma | |
DOID:8927 | learning disability | |
DOID:898 | autosomal dominant polycystic kidney disease | |
DOID:9220 | central sleep apnea | |
DOID:9306 | mechanical strabismus | |
DOID:934 | viral infectious disease |
HPO ID | HPO Term |
---|---|
HP:0007663 | Reduced visual acuity |
HP:0007675 | Progressive night blindness |
HP:0007772 | Impaired smooth pursuit |
HP:0007973 | Retinal dysplasia |
HP:0008872 | Feeding difficulties in infancy |
HP:0008915 | Childhood-onset truncal obesity |
HP:0010808 | Protruding tongue |
HP:0010828 | Hemifacial spasm |
HP:0010864 | Intellectual disability, severe |
HP:0011220 | Prominent forehead |
Disease ID | Disease Name |
---|---|
ORPHA:75858 |
|
ORPHA:475 |
|
OMIM:213300 |
|
ORPHA:220493 |
|
OMIM:610156 |
|
ORPHA:1454 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
118313688 | SCOMX33339 | ||
117031766 | RHIFE22142 | ||
100218296 | TAEGU06803 | ||
101814688 | FICAL06189 | ||
103239625 | CHLSB02884 | ||
104669671 | RHIRO02026 | ||
114588931 | PODMU25694 | ||
107552629 | SINGR74247 | ||
107587653 | SINGR23674 | ||
106845556 | EQUAS29286 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024