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:0110140 | Bardet-Biedl syndrome 18 | |
DOID:0110141 | Bardet-Biedl syndrome 19 | |
DOID:0110213 | isolated cleft palate | |
DOID:0110594 | primary ciliary dyskinesia 1 | |
DOID:0110861 | autosomal recessive polycystic kidney disease | |
DOID:0110980 | Joubert syndrome 1 | |
DOID:10426 | Klippel-Feil syndrome | |
DOID:10487 | Hirschsprung's disease | |
DOID:1056 | oculocerebrorenal syndrome | |
DOID:1059 | intellectual disability |
HPO ID | HPO Term |
---|---|
HP:0002421 | Poor head control |
HP:0002465 | Poor speech |
HP:0002508 | Brainstem dysplasia |
HP:0002553 | Highly arched eyebrow |
HP:0002612 | Congenital hepatic fibrosis |
HP:0002650 | Scoliosis |
HP:0002790 | Neonatal breathing dysregulation |
HP:0002793 | Abnormal pattern of respiration |
HP:0002871 | Central apnea |
HP:0002876 | Episodic tachypnea |
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