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GlyTouCan
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
LM-GlycoRepo
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:0050689 | brachydactyly-syndactyly syndrome | HGNC:5136 | Homo sapiens (human) | 3239 | HOXD13 |
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| DOID:4511 | breast angiosarcoma | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:1059 | intellectual disability | HGNC:12362 | Homo sapiens (human) | 7248 | TSC1 |
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| DOID:0112370 | Coffin-Siris syndrome 12 | HGNC:4332 | Homo sapiens (human) | 29998 | BICRA |
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| DOID:0060227 | Adams-Oliver syndrome | HGNC:19189 | Homo sapiens (human) | 57572 | DOCK6 |
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| DOID:0060940 | dystonia 33 | HGNC:9437 | Homo sapiens (human) | 5610 | EIF2AK2 |
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| DOID:4927 | Klatskin's tumor | HGNC:11110 | Homo sapiens (human) | 8289 | ARID1A |
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| DOID:3805 | porokeratosis | HGNC:7529 | Homo sapiens (human) | 4597 | MVD |
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| DOID:3526 | cerebral infarction | HGNC:7966 | Homo sapiens (human) | 10062 | NR1H3 |
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| DOID:0090052 | dystonia 24 | HGNC:14004 | Homo sapiens (human) | 63982 | ANO3 |
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| DOID:612 | primary immunodeficiency disease | HGNC:11491 | Homo sapiens (human) | 6850 | SYK |
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| DOID:0080419 | developmental and epileptic encephalopathy 50 | HGNC:1424 | Homo sapiens (human) | 790 | CAD |
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| DOID:9074 | systemic lupus erythematosus | HGNC:10907 | Homo sapiens (human) | 6556 | SLC11A1 |
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| DOID:12574 | posterior uveitis | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
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| DOID:0080855 | Parkinsonism | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0111067 | congenital bile acid synthesis defect 6 | HGNC:120 | Homo sapiens (human) | 8309 | ACOX2 |
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| DOID:2841 | asthma | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:1614 | male breast cancer | HGNC:16627 | Homo sapiens (human) | 11200 | CHEK2 |
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| DOID:9452 | steatotic liver disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:1612 | breast cancer | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:8986 | narcolepsy | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:2340 | craniosynostosis | HGNC:30000 | Homo sapiens (human) | 27241 | BBS9 |
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| DOID:5419 | schizophrenia | HGNC:13875 | Homo sapiens (human) | 93986 | FOXP2 |
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| DOID:2810 | middle lobe syndrome | HGNC:10524 | Homo sapiens (human) | 6299 | SALL1 |
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| DOID:9119 | acute myeloid leukemia | HGNC:13013 | Homo sapiens (human) | 7994 | KAT6A |
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