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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
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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB ▲ | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0112361 | spondylocostal dysostosis 3 | Xenbase:XB-GENE-865754 | Xenopus laevis (African clawed frog) | 100036937 | lfng.L |
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| DOID:12858 | Huntington's disease | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:11394 | adult respiratory distress syndrome | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:9352 | type 2 diabetes mellitus | MGI:1932139 | Mus musculus (house mouse) | 76055 | Oga |
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| DOID:14501 | Sjogren-Larsson syndrome | HGNC:411 | Homo sapiens (human) | 222 | ALDH3B2 |
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| DOID:10763 | hypertension | MGI:108083 | Mus musculus (house mouse) | 16535 | Kcnq1 |
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| DOID:8778 | Crohn's disease | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0110644 | long QT syndrome 1 | RGD:621503 | Rattus norvegicus (Norway rat) | 84020 | Kcnq1 |
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| DOID:0080572 | congenital disorder of glycosylation Iw | Xenbase:XB-GENE-17338795 | Xenopus laevis (African clawed frog) | 779022 | stt3a.S |
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| DOID:0080554 | congenital disorder of glycosylation Ib | SGD:S000000805 | Saccharomyces cerevisiae S288C | 856720 | PMI40 |
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| DOID:1380 | endometrial cancer | MGI:98898 | Mus musculus (house mouse) | 394436 | Ugt1a1 |
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| DOID:9206 | Barrett's esophagus | Xenbase:XB-GENE-17334879 | Xenopus laevis (African clawed frog) | 108716933 | b3gat2.L |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3770 | pulmonary fibrosis | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:2355 | anemia | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:10581 | metachromatic leukodystrophy | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:2738 | pseudoxanthoma elasticum | HGNC:15517 | Homo sapiens (human) | 64132 | XYLT2 |
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| DOID:12894 | Sjogren's syndrome | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:13544 | low tension glaucoma | MGI:87937 | Mus musculus (house mouse) | 11554 | Adrb1 |
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| DOID:10581 | metachromatic leukodystrophy | HGNC:713 | Homo sapiens (human) | 410 | ARSA |
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| DOID:399 | tuberculosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:552 | pneumonia | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:2747 | glycogen storage disease | HGNC:9725 | Homo sapiens (human) | 5836 | PYGL |
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| DOID:0050563 | nonsyndromic deafness | MGI:2146159 | Mus musculus (house mouse) | 380959 | Alg10b |
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| DOID:3393 | coronary artery disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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