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:10923 | sickle cell anemia | WB:WBGene00017089 | Caenorhabditis elegans | 171999 | poml-2 |
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DOID:10952 | nephritis | WB:WBGene00000039 | Caenorhabditis elegans | 180780 | acn-1 |
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DOID:783 | end stage renal disease | WB:WBGene00003407 | Caenorhabditis elegans | 180409 | mrp-1 |
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DOID:0112202 | developmental and epileptic encephalopathy | WB:WBGene00006783 | Caenorhabditis elegans | 176431 | unc-47 |
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DOID:9352 | type 2 diabetes mellitus | WB:WBGene00000776 | Caenorhabditis elegans | 180111 | cpl-1 |
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DOID:12270 | coloboma | WB:WBGene00002247 | Caenorhabditis elegans | 177292 | lam-1 |
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DOID:13241 | Behcet's disease | WB:WBGene00005644 | Caenorhabditis elegans | 178672 | srp-3 |
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DOID:0050474 | Netherton syndrome | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
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DOID:0080171 | esophageal atresia/tracheoesophageal fistula | WB:WBGene00006952 | Caenorhabditis elegans | 180638 | wrt-6 |
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DOID:0060462 | Desbuquois dysplasia | WB:WBGene00005024 | Caenorhabditis elegans | 190099 | sqv-6 |
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DOID:9256 | colorectal cancer | WB:WBGene00012185 | Caenorhabditis elegans | 180351 | W01F3.2 |
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DOID:0110942 | autosomal recessive osteopetrosis 1 | WB:WBGene00006914 | Caenorhabditis elegans | 177626 | vha-5 |
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DOID:3319 | lymphangioleiomyomatosis | WB:WBGene00001685 | Caenorhabditis elegans | 180601 | gpd-3 |
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DOID:3827 | congenital diaphragmatic hernia | WB:WBGene00008999 | Caenorhabditis elegans | 181229 | myrf-2 |
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DOID:2671 | transitional cell carcinoma | WB:WBGene00012782 | Caenorhabditis elegans | 177911 | Y43C5A.2 |
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DOID:2843 | long QT syndrome | WB:WBGene00006830 | Caenorhabditis elegans | 175527 | unc-103 |
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DOID:4195 | hyperglycemia | WB:WBGene00012185 | Caenorhabditis elegans | 180351 | W01F3.2 |
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DOID:557 | kidney disease | WB:WBGene00013855 | Caenorhabditis elegans | 179729 | cubn-1 |
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DOID:12217 | Lewy body dementia | WB:WBGene00006774 | Caenorhabditis elegans | 172105 | unc-38 |
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DOID:6039 | uveal melanoma | WB:WBGene00006894 | Caenorhabditis elegans | 175182 | ver-1 |
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DOID:1883 | hepatitis C | WB:WBGene00020481 | Caenorhabditis elegans | 174116 | gldi-2 |
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DOID:0111526 | Mullerian aplasia and hyperandrogenism | WB:WBGene00000857 | Caenorhabditis elegans | 173399 | cwn-1 |
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DOID:3803 | Crigler-Najjar syndrome | WB:WBGene00018206 | Caenorhabditis elegans | 185500 | ugt-61 |
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DOID:9261 | nasopharynx carcinoma | WB:WBGene00007517 | Caenorhabditis elegans | 182513 | gpx-3 |
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DOID:1657 | ventricular septal defect | 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