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:9352 | type 2 diabetes mellitus | WB:WBGene00004049 | Caenorhabditis elegans | 266823 | parp-1 |
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DOID:0050156 | idiopathic pulmonary fibrosis | WB:WBGene00004049 | Caenorhabditis elegans | 266823 | parp-1 |
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DOID:1074 | kidney failure | WB:WBGene00004049 | Caenorhabditis elegans | 266823 | parp-1 |
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DOID:12858 | Huntington's disease | WB:WBGene00004049 | Caenorhabditis elegans | 266823 | parp-1 |
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DOID:10534 | stomach cancer | WB:WBGene00004049 | Caenorhabditis elegans | 266823 | parp-1 |
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DOID:3525 | middle cerebral artery infarction | WB:WBGene00004049 | Caenorhabditis elegans | 266823 | parp-1 |
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DOID:10952 | nephritis | WB:WBGene00004049 | Caenorhabditis elegans | 266823 | parp-1 |
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DOID:127 | leiomyoma | WB:WBGene00004049 | Caenorhabditis elegans | 266823 | parp-1 |
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DOID:417 | autoimmune disease | WB:WBGene00004049 | Caenorhabditis elegans | 266823 | parp-1 |
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DOID:8677 | perinatal necrotizing enterocolitis | WB:WBGene00004049 | Caenorhabditis elegans | 266823 | parp-1 |
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DOID:5154 | borna disease | WB:WBGene00004049 | Caenorhabditis elegans | 266823 | parp-1 |
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DOID:224 | transient cerebral ischemia | WB:WBGene00004049 | Caenorhabditis elegans | 266823 | parp-1 |
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DOID:1168 | familial hyperlipidemia | HGNC:4241 | Homo sapiens (human) | 2673 | GFPT1 |
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DOID:9970 | obesity | HGNC:4241 | Homo sapiens (human) | 2673 | GFPT1 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:4241 | Homo sapiens (human) | 2673 | GFPT1 |
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DOID:0110660 | congenital myasthenic syndrome 12 | HGNC:4241 | Homo sapiens (human) | 2673 | GFPT1 |
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DOID:1440 | Machado-Joseph disease | HGNC:4241 | Homo sapiens (human) | 2673 | GFPT1 |
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DOID:2018 | hyperinsulinism | HGNC:4241 | Homo sapiens (human) | 2673 | GFPT1 |
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DOID:0080855 | Parkinsonism | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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DOID:3049 | Churg-Strauss syndrome | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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DOID:2316 | brain ischemia | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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DOID:11446 | sciatic neuropathy | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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DOID:10487 | Hirschsprung's disease | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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DOID:9810 | polyarteritis nodosa | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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DOID:14766 | renal agenesis | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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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