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:0110679 | congenital myasthenic syndrome 4C | RGD:2353 | Rattus norvegicus (Norway rat) | 29422 | Chrne |
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DOID:9744 | type 1 diabetes mellitus | RGD:67378 | Rattus norvegicus (Norway rat) | 24586 | Ncam1 |
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DOID:8577 | ulcerative colitis | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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DOID:5742 | pancreatic acinar cell adenocarcinoma | HGNC:11283 | Homo sapiens (human) | 6714 | SRC |
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DOID:0060060 | non-Hodgkin lymphoma | MGI:96392 | Mus musculus (house mouse) | 15894 | Icam1 |
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DOID:783 | end stage renal disease | SGD:S000004540 | Saccharomyces cerevisiae S288C | 854900 | HMG1 |
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DOID:0060037 | developmental disorder of mental health | HGNC:26129 | Homo sapiens (human) | 64926 | RASAL3 |
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DOID:0110865 | congenital stationary night blindness 1B | WB:WBGene00003232 | Caenorhabditis elegans | 191707 | mgl-1 |
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DOID:0080162 | lupus nephritis | HGNC:6371 | Homo sapiens (human) | 3818 | KLKB1 |
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DOID:684 | hepatocellular carcinoma | MGI:88342 | Mus musculus (house mouse) | 12514 | Cd68 |
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DOID:7148 | rheumatoid arthritis | HGNC:5253 | Homo sapiens (human) | 3320 | HSP90AA1 |
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DOID:0060074 | ductal carcinoma in situ | MGI:97011 | Mus musculus (house mouse) | 17395 | Mmp9 |
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DOID:0110245 | cataract 38 | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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DOID:0080563 | congenital disorder of glycosylation Ik | Xenbase:XB-GENE-1006367 | Xenopus laevis (African clawed frog) | 100037043 | alg1.L |
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DOID:850 | lung disease | WB:WBGene00016570 | Caenorhabditis elegans | 180841 | gnrr-4 |
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DOID:1932 | Angelman syndrome | HGNC:12496 | Homo sapiens (human) | 7337 | UBE3A |
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DOID:11054 | urinary bladder cancer | RGD:2081 | Rattus norvegicus (Norway rat) | 24185 | Akt1 |
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DOID:12120 | pulmonary alveolar proteinosis | HGNC:6898 | Homo sapiens (human) | 4141 | MARS1 |
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DOID:0050861 | colorectal adenocarcinoma | WB:WBGene00006897 | Caenorhabditis elegans | 186632 | ver-4 |
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DOID:3525 | middle cerebral artery infarction | MGI:95755 | Mus musculus (house mouse) | 20525 | Slc2a1 |
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DOID:9351 | diabetes mellitus | HGNC:10632 | Homo sapiens (human) | 6352 | CCL5 |
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DOID:9452 | steatotic liver disease | HGNC:7794 | Homo sapiens (human) | 4790 | NFKB1 |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | SGD:S000000036 | Saccharomyces cerevisiae S288C | 851193 | CDC19 |
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DOID:2377 | multiple sclerosis | MGI:97309 | Mus musculus (house mouse) | 380684 | Nefh |
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DOID:3371 | chondrosarcoma | Xenbase:XB-GENE-867536 | Xenopus laevis (African clawed frog) | 399115 | ext1.S |
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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