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:7147 | ankylosing spondylitis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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DOID:1184 | nephrotic syndrome | RGD:620925 | Rattus norvegicus (Norway rat) | 83516 | Ppargc1a |
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DOID:2560 | morphine dependence | RGD:1598328 | Rattus norvegicus (Norway rat) | 310738 | Ngf |
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DOID:10591 | pre-eclampsia | HGNC:2606 | Homo sapiens (human) | 1594 | CYP27B1 |
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DOID:10591 | pre-eclampsia | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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DOID:10591 | pre-eclampsia | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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DOID:0080006 | bone development disease | MGI:97372 | Mus musculus (house mouse) | 230103 | Npr2 |
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DOID:0060770 | dextro-looped transposition of the great arteries | HGNC:10937 | Homo sapiens (human) | 6573 | SLC19A1 |
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DOID:13207 | proliferative diabetic retinopathy | HGNC:3763 | Homo sapiens (human) | 2321 | FLT1 |
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DOID:224 | transient cerebral ischemia | RGD:621842 | Rattus norvegicus (Norway rat) | 116479 | F11r |
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DOID:13207 | proliferative diabetic retinopathy | HGNC:3357 | Homo sapiens (human) | 5168 | ENPP2 |
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DOID:5162 | arteriolosclerosis | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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DOID:9744 | type 1 diabetes mellitus | HGNC:11740 | Homo sapiens (human) | 7018 | TF |
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DOID:1059 | intellectual disability | WB:WBGene00003182 | Caenorhabditis elegans | 172732 | mef-2 |
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DOID:0060041 | autism spectrum disorder | WB:WBGene00003182 | Caenorhabditis elegans | 172732 | mef-2 |
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DOID:0060704 | lymphoproliferative syndrome | HGNC:11364 | Homo sapiens (human) | 6774 | STAT3 |
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DOID:9256 | colorectal cancer | RGD:620360 | Rattus norvegicus (Norway rat) | 83619 | Nfe2l2 |
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DOID:10887 | lepromatous leprosy | HGNC:1631 | Homo sapiens (human) | 9332 | CD163 |
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DOID:0050835 | generalized dystonia | MGI:109482 | Mus musculus (house mouse) | 12286 | Cacna1a |
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DOID:0080162 | lupus nephritis | HGNC:11917 | Homo sapiens (human) | 7133 | TNFRSF1B |
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DOID:9256 | colorectal cancer | HGNC:11896 | Homo sapiens (human) | 7128 | TNFAIP3 |
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DOID:10591 | pre-eclampsia | HGNC:4910 | Homo sapiens (human) | 3091 | HIF1A |
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DOID:10591 | pre-eclampsia | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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DOID:12306 | vitiligo | HGNC:12442 | Homo sapiens (human) | 7299 | TYR |
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DOID:1909 | melanoma | HGNC:12442 | Homo sapiens (human) | 7299 | TYR |
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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
This work is licensed under Creative Commons Attribution 4.0 International
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Last updated: February 17, 2025