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:607 | paraplegia | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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DOID:0111156 | spermatogenic failure 9 | ZFIN:ZDB-GENE-030521-11 | Danio rerio (zebrafish) | 368327 | dpy19l1l |
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DOID:0080162 | lupus nephritis | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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DOID:12783 | migraine without aura | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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DOID:10763 | hypertension | MGI:88470 | Mus musculus (house mouse) | 12846 | Comt |
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DOID:3323 | Sandhoff disease | MGI:96074 | Mus musculus (house mouse) | 15212 | Hexb |
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DOID:9970 | obesity | SGD:S000005646 | Saccharomyces cerevisiae S288C | 854287 | GCY1 |
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DOID:0050985 | spinocerebellar ataxia type 38 | HGNC:21308 | Homo sapiens (human) | 60481 | ELOVL5 |
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DOID:0080005 | bone remodeling disease | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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DOID:3748 | esophagus squamous cell carcinoma | RGD:2081 | Rattus norvegicus (Norway rat) | 24185 | Akt1 |
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DOID:11476 | osteoporosis | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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DOID:6432 | pulmonary hypertension | HGNC:4818 | Homo sapiens (human) | 3036 | HAS1 |
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DOID:10584 | retinitis pigmentosa | HGNC:4922 | Homo sapiens (human) | 3098 | HK1 |
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DOID:4450 | renal cell carcinoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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DOID:0050719 | cerebral folate receptor alpha deficiency | HGNC:3791 | Homo sapiens (human) | 2348 | FOLR1 |
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DOID:9352 | type 2 diabetes mellitus | MGI:2153588 | Mus musculus (house mouse) | 140491 | Ppp1r3a |
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DOID:8466 | retinal degeneration | WB:WBGene00000833 | Caenorhabditis elegans | 176437 | cts-1 |
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DOID:12858 | Huntington's disease | WB:WBGene00004049 | Caenorhabditis elegans | 266823 | parp-1 |
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DOID:2580 | rhizomelic chondrodysplasia punctata | HGNC:327 | Homo sapiens (human) | 8540 | AGPS |
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DOID:10534 | stomach cancer | WB:WBGene00004049 | Caenorhabditis elegans | 266823 | parp-1 |
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DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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DOID:3534 | Lafora disease | RGD:1589798 | Rattus norvegicus (Norway rat) | 690987 | Gys1 |
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DOID:12053 | cryptococcosis | RGD:1303058 | Rattus norvegicus (Norway rat) | 113901 | Chia |
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DOID:684 | hepatocellular carcinoma | SGD:S000000257 | Saccharomyces cerevisiae S288C | 852342 | YBR053C |
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DOID:11832 | visual epilepsy | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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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