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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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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:0050328 | congenital hypothyroidism | HGNC:8622 | Homo sapiens (human) | 7849 | PAX8 |
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| DOID:11555 | Fuchs' endothelial dystrophy | HGNC:2216 | Homo sapiens (human) | 1296 | COL8A2 |
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| DOID:0070472 | early-onset epilepsy 3 | HGNC:855 | Homo sapiens (human) | 527 | ATP6V0C |
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| DOID:12449 | aplastic anemia | HGNC:5438 | Homo sapiens (human) | 3458 | IFNG |
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| DOID:4621 | holoprosencephaly | HGNC:11776 | Homo sapiens (human) | 7050 | TGIF1 |
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| DOID:0060020 | reticular dysgenesis | HGNC:362 | Homo sapiens (human) | 204 | AK2 |
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| DOID:11759 | hypochromic anemia | HGNC:10908 | Homo sapiens (human) | 4891 | SLC11A2 |
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| DOID:0060013 | X-linked severe combined immunodeficiency | HGNC:6010 | Homo sapiens (human) | 3561 | IL2RG |
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| DOID:0111035 | CADASIL 1 | HGNC:7883 | Homo sapiens (human) | 4854 | NOTCH3 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:0110205 | Charcot-Marie-Tooth disease dominant intermediate E | HGNC:23791 | Homo sapiens (human) | 64423 | INF2 |
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| DOID:0110964 | brachydactyly type A1 | HGNC:5956 | Homo sapiens (human) | 3549 | IHH |
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| DOID:0110255 | cataract 5 multiple types | HGNC:5227 | Homo sapiens (human) | 3299 | HSF4 |
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| DOID:0060365 | mandibulofacial dysostosis with alopecia | HGNC:3179 | Homo sapiens (human) | 1909 | EDNRA |
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| DOID:0090003 | agenesis of the corpus callosum with peripheral neuropathy | HGNC:10914 | Homo sapiens (human) | 9990 | SLC12A6 |
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| DOID:0050773 | paraganglioma | HGNC:10683 | Homo sapiens (human) | 6392 | SDHD |
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| DOID:7693 | abdominal aortic aneurysm | HGNC:3327 | Homo sapiens (human) | 2006 | ELN |
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| DOID:3144 | cutis laxa | HGNC:3602 | Homo sapiens (human) | 10516 | FBLN5 |
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| DOID:0110779 | hereditary spastic paraplegia 28 | HGNC:19714 | Homo sapiens (human) | 80821 | DDHD1 |
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| DOID:0070341 | neonatal-onset type II citrullinemia | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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| DOID:12365 | malaria | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:1935 | Bardet-Biedl syndrome | HGNC:967 | Homo sapiens (human) | 583 | BBS2 |
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| DOID:0110310 | hypertrophic cardiomyopathy 4 | HGNC:7551 | Homo sapiens (human) | 4607 | MYBPC3 |
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| DOID:10652 | Alzheimer's disease | HGNC:8032 | Homo sapiens (human) | 4915 | NTRK2 |
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| DOID:0060787 | hypomyelinating leukodystrophy 2 | HGNC:17494 | Homo sapiens (human) | 57165 | GJC2 |
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