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 |
---|---|---|
basal cortex | ||
motile cilium | ||
ciliary basal body | ||
endoplasmic reticulum | ||
cytosol |
GO Term | Evidence Code | PMID |
---|---|---|
transcription regulator inhibitor activity | ||
voltage-gated calcium channel activity | ||
protein homodimerization activity | ||
calcium-induced calcium release activity | ||
voltage-gated potassium channel activity |
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 |
---|---|---|---|
101957318 | ICTTR02189 | ||
101609962 | JACJA13123 | ||
117021997 | RHIFE18814 | ||
100219153 | TAEGU23358 | ||
108544701 | RHIBE39756 | ||
104664612 | RHIRO40954 | ||
100594714 | NOMLE37957 | ||
114603974 | PODMU30365 | ||
107583176 | SINGR31286 | ||
107594434 | SINGR54266 |
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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