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 | July 29, 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:438 | autoimmune disease of the nervous system | WB:WBGene00017166 | Caenorhabditis elegans | 175827 | aldo-2 |
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DOID:9744 | type 1 diabetes mellitus | WB:WBGene00010904 | Caenorhabditis elegans | 175591 | ugt-62 |
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DOID:9352 | type 2 diabetes mellitus | WB:WBGene00010904 | Caenorhabditis elegans | 175591 | ugt-62 |
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DOID:3803 | Crigler-Najjar syndrome | WB:WBGene00010904 | Caenorhabditis elegans | 175591 | ugt-62 |
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DOID:2741 | bilirubin metabolic disorder | WB:WBGene00010904 | Caenorhabditis elegans | 175591 | ugt-62 |
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DOID:7998 | hyperthyroidism | WB:WBGene00010904 | Caenorhabditis elegans | 175591 | ugt-62 |
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DOID:0111459 | classic galactosemia | WB:WBGene00014203 | Caenorhabditis elegans | 175506 | ZK1058.3 |
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DOID:9870 | galactosemia | WB:WBGene00014203 | Caenorhabditis elegans | 175506 | ZK1058.3 |
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DOID:332 | amyotrophic lateral sclerosis | WB:WBGene00006575 | Caenorhabditis elegans | 175502 | tir-1 |
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DOID:1289 | neurodegenerative disease | WB:WBGene00006575 | Caenorhabditis elegans | 175502 | tir-1 |
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DOID:5212 | congenital disorder of glycosylation | WB:WBGene00010720 | Caenorhabditis elegans | 175065 | algn-3 |
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DOID:0080556 | congenital disorder of glycosylation Id | WB:WBGene00010720 | Caenorhabditis elegans | 175065 | algn-3 |
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DOID:3211 | lysosomal storage disease | HGNC:318 | Homo sapiens (human) | 175 | AGA |
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DOID:0050461 | aspartylglucosaminuria | HGNC:318 | Homo sapiens (human) | 175 | AGA |
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DOID:1287 | cardiovascular system disease | WB:WBGene00001793 | Caenorhabditis elegans | 174924 | gsy-1 |
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DOID:2747 | glycogen storage disease | WB:WBGene00001793 | Caenorhabditis elegans | 174924 | gsy-1 |
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DOID:3534 | Lafora disease | WB:WBGene00001793 | Caenorhabditis elegans | 174924 | gsy-1 |
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DOID:0080564 | congenital disorder of glycosylation Il | WB:WBGene00007556 | Caenorhabditis elegans | 174633 | algn-9 |
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DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00007556 | Caenorhabditis elegans | 174633 | algn-9 |
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DOID:3319 | lymphangioleiomyomatosis | WB:WBGene00001683 | Caenorhabditis elegans | 174603 | gpd-1 |
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DOID:0050827 | rheumatic heart disease | WB:WBGene00001683 | Caenorhabditis elegans | 174603 | gpd-1 |
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DOID:9970 | obesity | WB:WBGene00001683 | Caenorhabditis elegans | 174603 | gpd-1 |
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DOID:0060108 | brain glioma | WB:WBGene00001683 | Caenorhabditis elegans | 174603 | gpd-1 |
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DOID:10652 | Alzheimer's disease | WB:WBGene00001683 | Caenorhabditis elegans | 174603 | gpd-1 |
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DOID:8947 | diabetic retinopathy | WB:WBGene00001683 | Caenorhabditis elegans | 174603 | gpd-1 |
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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 v4.0.0
Last updated: August 19, 2024