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:0001395 | Hepatic fibrosis |
HP:0001409 | Portal hypertension |
HP:0001651 | Dextrocardia |
HP:0001696 | Situs inversus totalis |
HP:0001744 | Splenomegaly |
HP:0001829 | Foot polydactyly |
HP:0001830 | Postaxial foot polydactyly |
HP:0001956 | Truncal obesity |
HP:0002084 | Encephalocele |
HP:0002085 | Occipital encephalocele |
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 |
---|---|---|---|
116817507 | CHEAB00605 | ||
105298576 | PTEVA08326 | ||
115048613 | ECHNA21490 | ||
115398351 | SALFA06432 | ||
113486499 | ATHCN17807 | ||
105818699 | PROCO27662 | ||
109078005 | CYPCA12490 | ||
103741211 | NANGA21143 | ||
116454341 | CORMO10662 | ||
115616951 | STRHB17768 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
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