Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
Source | Last Updated |
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Alliance of Genome Resources | October 9, 2024 |
Disease ID | Disease Name | Alliance of Genome Resources ID ▲ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
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DOID:0050477 | Liddle syndrome | WB:WBGene00012137 | Caenorhabditis elegans | 189058 | asic-2 |
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DOID:4479 | pseudohypoaldosteronism | WB:WBGene00012137 | Caenorhabditis elegans | 189058 | asic-2 |
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DOID:0080528 | bronchiectasis 3 | WB:WBGene00012137 | Caenorhabditis elegans | 189058 | asic-2 |
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DOID:75 | lymphatic system disease | WB:WBGene00012144 | Caenorhabditis elegans | 179714 | lgmn-1 |
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DOID:0070221 | progressive familial intrahepatic cholestasis | WB:WBGene00012182 | Caenorhabditis elegans | 175140 | osta-3 |
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DOID:0060419 | chromosome 3q29 microdeletion syndrome | WB:WBGene00012182 | Caenorhabditis elegans | 175140 | osta-3 |
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DOID:0050861 | colorectal adenocarcinoma | WB:WBGene00012184 | Caenorhabditis elegans | 180350 | mnr-1 |
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DOID:0080933 | immunoglobulin light chain amyloidosis | WB:WBGene00012185 | Caenorhabditis elegans | 180351 | W01F3.2 |
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DOID:0050865 | tongue squamous cell carcinoma | WB:WBGene00012185 | Caenorhabditis elegans | 180351 | W01F3.2 |
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DOID:3908 | lung non-small cell carcinoma | WB:WBGene00012185 | Caenorhabditis elegans | 180351 | W01F3.2 |
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DOID:13241 | Behcet's disease | WB:WBGene00012185 | Caenorhabditis elegans | 180351 | W01F3.2 |
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DOID:8869 | neuromyelitis optica | WB:WBGene00012185 | Caenorhabditis elegans | 180351 | W01F3.2 |
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DOID:13810 | familial hypercholesterolemia | WB:WBGene00012185 | Caenorhabditis elegans | 180351 | W01F3.2 |
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DOID:14261 | fragile X syndrome | WB:WBGene00012185 | Caenorhabditis elegans | 180351 | W01F3.2 |
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DOID:0050700 | cardiomyopathy | WB:WBGene00012185 | Caenorhabditis elegans | 180351 | W01F3.2 |
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DOID:8923 | skin melanoma | WB:WBGene00012185 | Caenorhabditis elegans | 180351 | W01F3.2 |
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DOID:106 | pleural tuberculosis | WB:WBGene00012185 | Caenorhabditis elegans | 180351 | W01F3.2 |
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DOID:9470 | bacterial meningitis | WB:WBGene00012185 | Caenorhabditis elegans | 180351 | W01F3.2 |
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DOID:10976 | membranous glomerulonephritis | WB:WBGene00012185 | Caenorhabditis elegans | 180351 | W01F3.2 |
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DOID:12236 | primary biliary cholangitis | WB:WBGene00012185 | Caenorhabditis elegans | 180351 | W01F3.2 |
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DOID:3407 | carotid artery disease | WB:WBGene00012185 | Caenorhabditis elegans | 180351 | W01F3.2 |
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DOID:4914 | esophagus adenocarcinoma | WB:WBGene00012185 | Caenorhabditis elegans | 180351 | W01F3.2 |
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DOID:1727 | retinal vein occlusion | WB:WBGene00012185 | Caenorhabditis elegans | 180351 | W01F3.2 |
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DOID:9352 | type 2 diabetes mellitus | WB:WBGene00012185 | Caenorhabditis elegans | 180351 | W01F3.2 |
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DOID:3319 | lymphangioleiomyomatosis | WB:WBGene00012185 | Caenorhabditis elegans | 180351 | W01F3.2 |
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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 v4.1.0
Last updated: December 9, 2024