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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Repository for lectin-assisted multimodality data
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Alliance of Genome Resources
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 |
|---|---|
| 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 |
|---|---|---|---|---|---|---|---|---|
| DOID:0060540 | Hermansky-Pudlak syndrome 2 | HGNC:566 | Homo sapiens (human) | 8546 | AP3B1 |
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| DOID:14330 | Parkinson's disease | HGNC:30022 | Homo sapiens (human) | 133522 | PPARGC1B |
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| DOID:0080162 | lupus nephritis | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:0081276 | cerebellar atrophy, visual impairment, and psychomotor retardation | MGI:2443696 | Mus musculus (house mouse) | 230866 | Emc1 |
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| DOID:0060480 | left ventricular noncompaction | HGNC:20862 | Homo sapiens (human) | 64116 | SLC39A8 |
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| DOID:3021 | acute kidney failure | HGNC:775 | Homo sapiens (human) | 462 | SERPINC1 |
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| DOID:321 | tropical spastic paraparesis | HGNC:7794 | Homo sapiens (human) | 4790 | NFKB1 |
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| DOID:0070218 | familial hyperinsulinemic hypoglycemia 2 | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:3892 | insulinoma | HGNC:11006 | Homo sapiens (human) | 6514 | SLC2A2 |
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| DOID:9952 | acute lymphoblastic leukemia | MGI:97570 | Mus musculus (house mouse) | 18671 | Abcb1a |
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| DOID:0110023 | age related macular degeneration 11 | MGI:102519 | Mus musculus (house mouse) | 13010 | Cst3 |
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| DOID:1441 | autosomal dominant cerebellar ataxia | MGI:96624 | Mus musculus (house mouse) | 16440 | Itpr3 |
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| DOID:9119 | acute myeloid leukemia | HGNC:11180 | Homo sapiens (human) | 6648 | SOD2 |
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| DOID:10459 | common cold | MGI:2676324 | Mus musculus (house mouse) | 242519 | Ifna12 |
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| DOID:3021 | acute kidney failure | FB:FBgn0028988 | Drosophila melanogaster (fruit fly) | 49808 | Spn42Dd |
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| DOID:9255 | frontotemporal dementia | MGI:97313 | Mus musculus (house mouse) | 18039 | Nefl |
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| DOID:1826 | epilepsy | RGD:2651 | Rattus norvegicus (Norway rat) | 24922 | Gabrb3 |
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| DOID:0080552 | congenital disorder of glycosylation Ia | MGI:1353418 | Mus musculus (house mouse) | 29858 | Pmm1 |
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| DOID:0112245 | focal segmental glomerulosclerosis 3 | HGNC:14258 | Homo sapiens (human) | 23607 | CD2AP |
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| DOID:10584 | retinitis pigmentosa | ZFIN:ZDB-GENE-990415-271 | Danio rerio (zebrafish) | 30295 | rho |
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| DOID:576 | proteinuria | MGI:104850 | Mus musculus (house mouse) | 13136 | Cd55 |
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| DOID:0060811 | syndromic X-linked intellectual disability Turner type | HGNC:30892 | Homo sapiens (human) | 10075 | HUWE1 |
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| DOID:6432 | pulmonary hypertension | HGNC:11772 | Homo sapiens (human) | 7046 | TGFBR1 |
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| DOID:8725 | vascular dementia | HGNC:894 | Homo sapiens (human) | 551 | AVP |
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| DOID:3908 | lung non-small cell carcinoma | RGD:69062 | Rattus norvegicus (Norway rat) | 83571 | Cdkn1b |
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