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 |
---|---|---|---|
115540593 | GADMO41168 | ||
100192346 | ORYLA00443 | ||
100701939 | ORENI63504 | ||
115591125 | SPAAU56262 | ||
108711015 | Xenbase:XB-GENE-17342095 | ||
100038156 | Xenbase:XB-GENE-482111 | ||
101931008 | CHRPI11485 | ||
109322153 | CROPO11789 | ||
113434855 | PSETE05661 | ||
100917024 | SARHA16772 |
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