GO Term | Evidence Code | PMID |
---|---|---|
negative regulation of G1/S transition of mitotic cell cycle | ||
metanephric smooth muscle tissue development | ||
aorta development | ||
negative regulation of cell population proliferation |
|
|
negative regulation of ryanodine-sensitive calcium-release channel activity |
GO Term | Evidence Code | PMID |
---|---|---|
basal cortex | ||
motile cilium | ||
ciliary basal body | ||
endoplasmic reticulum | ||
cytosol |
GO Term | Evidence Code | PMID |
---|---|---|
cytoskeletal protein binding | ||
ATPase binding | ||
monoatomic cation channel activity | ||
calcium channel activity | ||
muscle alpha-actinin binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0060041 | autism spectrum disorder | |
DOID:0060224 | atrial fibrillation | |
DOID:0060340 | ciliopathy | |
DOID:0070115 | Meckel syndrome 1 | |
DOID:0070116 | Meckel syndrome 2 | |
DOID:0070117 | Meckel syndrome 3 | |
DOID:0070118 | Meckel syndrome 4 | |
DOID:0070119 | Meckel syndrome 5 | |
DOID:0070120 | Meckel syndrome 6 | |
DOID:0070122 | Meckel syndrome 8 |
HPO ID | HPO Term |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000010 | Recurrent urinary tract infections |
HP:0000083 | Renal insufficiency |
HP:0000105 | Enlarged kidney |
HP:0000107 | Renal cyst |
HP:0000113 | Polycystic kidney dysplasia |
HP:0000324 | Facial asymmetry |
HP:0000790 | Hematuria |
HP:0000791 | Uric acid nephrolithiasis |
HP:0000822 | Hypertension |
Disease ID | Disease Name |
---|---|
ORPHA:730 |
|
OMIM:613095 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100411856 | CALJA29362 | ||
105576752 | CERAT13448 | ||
702179 | MACMU36998 | ||
105479647 | MACNE18355 | ||
101016289 | PAPAN28490 | ||
101141005 | GORGO30814 | ||
461367 | PANTR34093 | ||
100462082 | PONAB27608 | ||
112919562 | VULVU11866 | ||
101672143 | MUSPF11963 |
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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