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:0070115 | Meckel syndrome 1 | |
DOID:0080212 | polycystic kidney disease 4 | |
DOID:0090053 | episodic kinesigenic dyskinesia 1 | |
DOID:0110123 | Bardet-Biedl syndrome 1 | |
DOID:0110124 | Bardet-Biedl syndrome 2 | |
DOID:0110125 | Bardet-Biedl syndrome 3 | |
DOID:0110126 | Bardet-Biedl syndrome 4 | |
DOID:0110127 | Bardet-Biedl syndrome 5 | |
DOID:0110128 | Bardet-Biedl syndrome 6 | |
DOID:0110129 | Bardet-Biedl syndrome 7 |
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 |
---|---|---|---|
607443 | CANLF19266 | ||
112906951 | VULVU32419 | ||
123796350 | URSAM17330 | ||
100468432 | AILME07197 | ||
101677772 | MUSPF11443 | ||
101093901 | FELCA29855 | ||
122204727 | PANLE26132 | ||
100670120 | LOXAF00423 | ||
100068731 | HORSE23894 | ||
110258074 | PIGXX38804 |
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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