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GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
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:0080600 | COVID-19 | HGNC:1328 | Homo sapiens (human) | 725 | C4BPB |
|
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| DOID:1459 | hypothyroidism | HGNC:13273 | Homo sapiens (human) | 50506 | DUOX2 |
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| DOID:0050338 | primary bacterial infectious disease | HGNC:13273 | Homo sapiens (human) | 50506 | DUOX2 |
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| DOID:0112189 | thyroid dyshormonogenesis 6 | HGNC:13273 | Homo sapiens (human) | 50506 | DUOX2 |
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| DOID:9281 | phenylketonuria | HGNC:13273 | Homo sapiens (human) | 50506 | DUOX2 |
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| DOID:1498 | cholera | HGNC:13273 | Homo sapiens (human) | 50506 | DUOX2 |
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| DOID:8778 | Crohn's disease | HGNC:13273 | Homo sapiens (human) | 50506 | DUOX2 |
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| DOID:0050328 | congenital hypothyroidism | HGNC:13273 | Homo sapiens (human) | 50506 | DUOX2 |
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| DOID:8577 | ulcerative colitis | HGNC:13273 | Homo sapiens (human) | 50506 | DUOX2 |
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| DOID:0112034 | non-syndromic X-linked intellectual disability 9 | HGNC:13254 | Homo sapiens (human) | 24140 | FTSJ1 |
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| DOID:0050776 | non-syndromic X-linked intellectual disability | HGNC:13254 | Homo sapiens (human) | 24140 | FTSJ1 |
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| DOID:0080600 | COVID-19 | HGNC:1325 | Homo sapiens (human) | 722 | C4BPA |
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| DOID:12361 | Graves' disease | HGNC:1324 | Homo sapiens (human) | 721 | C4B |
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| DOID:9074 | systemic lupus erythematosus | HGNC:1324 | Homo sapiens (human) | 721 | C4B |
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| DOID:0060298 | complement component 4b deficiency | HGNC:1324 | Homo sapiens (human) | 721 | C4B |
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| DOID:12849 | autistic disorder | HGNC:1324 | Homo sapiens (human) | 721 | C4B |
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| DOID:4450 | renal cell carcinoma | HGNC:1324 | Homo sapiens (human) | 721 | C4B |
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| DOID:7148 | rheumatoid arthritis | HGNC:1324 | Homo sapiens (human) | 721 | C4B |
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| DOID:4450 | renal cell carcinoma | HGNC:1323 | Homo sapiens (human) | 720 | C4A |
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| DOID:12361 | Graves' disease | HGNC:1323 | Homo sapiens (human) | 720 | C4A |
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| DOID:12306 | vitiligo | HGNC:1323 | Homo sapiens (human) | 720 | C4A |
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| DOID:0060297 | complement component 4a deficiency | HGNC:1323 | Homo sapiens (human) | 720 | C4A |
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| DOID:9074 | systemic lupus erythematosus | HGNC:1323 | Homo sapiens (human) | 720 | C4A |
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| DOID:0060038 | specific developmental disorder | HGNC:13222 | Homo sapiens (human) | 64919 | BCL11B |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:13222 | Homo sapiens (human) | 64919 | BCL11B |
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