GO Term | Evidence Code | PMID |
---|---|---|
determination of liver left/right asymmetry | ||
metanephric ascending thin limb development | ||
cellular response to calcium ion | ||
branching involved in ureteric bud morphogenesis | ||
embryonic placenta development |
GO Term | Evidence Code | PMID |
---|---|---|
Golgi apparatus | ||
polycystin complex | ||
ciliary membrane | ||
extracellular exosome | ||
basolateral plasma membrane |
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:4676 | uremia | |
DOID:4766 | embryoma | |
DOID:0050424 | familial adenomatous polyposis | |
DOID:0050156 | idiopathic pulmonary fibrosis | |
DOID:0050646 | distal arthrogryposis | |
DOID:0050770 | polycystic liver disease | |
DOID:0050771 | pheochromocytoma | |
DOID:0050778 | Meckel syndrome | |
DOID:0050820 | atrioventricular block | |
DOID:0050997 | cerebellar ataxia, mental retardation and dysequlibrium syndrome |
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 |
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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