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:11476 | osteoporosis | HGNC:2593 | Homo sapiens (human) | 1586 | CYP17A1 |
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DOID:0050453 | lissencephaly | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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DOID:1059 | intellectual disability | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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DOID:10159 | osteonecrosis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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DOID:14067 | Plasmodium falciparum malaria | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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DOID:2841 | asthma | HGNC:15634 | Homo sapiens (human) | 81793 | TLR10 |
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DOID:3393 | coronary artery disease | HGNC:94 | Homo sapiens (human) | 39 | ACAT2 |
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DOID:10652 | Alzheimer's disease | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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DOID:399 | tuberculosis | HGNC:2615 | Homo sapiens (human) | 1555 | CYP2B6 |
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DOID:9383 | iridocyclitis | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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DOID:5419 | schizophrenia | HGNC:6470 | Homo sapiens (human) | 3897 | L1CAM |
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DOID:1588 | thrombocytopenia | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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DOID:3146 | lipid metabolism disorder | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
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DOID:1612 | breast cancer | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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DOID:3393 | coronary artery disease | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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DOID:3649 | pyruvate decarboxylase deficiency | HGNC:21350 | Homo sapiens (human) | 8050 | PDHX |
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DOID:6364 | migraine | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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DOID:0060448 | Fleck corneal dystrophy | HGNC:23785 | Homo sapiens (human) | 200576 | PIKFYVE |
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DOID:2349 | arteriosclerosis | HGNC:435 | Homo sapiens (human) | 240 | ALOX5 |
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DOID:13544 | low tension glaucoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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DOID:1825 | childhood absence epilepsy | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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DOID:10892 | hypospadias | HGNC:11285 | Homo sapiens (human) | 6716 | SRD5A2 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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DOID:5844 | myocardial infarction | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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DOID:12849 | autistic disorder | HGNC:8978 | Homo sapiens (human) | 5294 | PIK3CG |
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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