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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
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:10608 | celiac disease | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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| DOID:1495 | cystic echinococcosis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:9620 | vesicoureteral reflux | HGNC:10250 | Homo sapiens (human) | 6092 | ROBO2 |
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| DOID:10923 | sickle cell anemia | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
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| DOID:3371 | chondrosarcoma | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:10887 | lepromatous leprosy | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:11664 | nephrosclerosis | HGNC:285 | Homo sapiens (human) | 153 | ADRB1 |
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| DOID:10763 | hypertension | HGNC:4893 | Homo sapiens (human) | 3082 | HGF |
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| DOID:0111239 | congenital muscular dystrophy-dystroglycanopathy type A10 | HGNC:13530 | Homo sapiens (human) | 10329 | RXYLT1 |
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| DOID:14557 | primary pulmonary hypertension | HGNC:6278 | Homo sapiens (human) | 3777 | KCNK3 |
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| DOID:0080333 | aortic valve disease 1 | HGNC:7881 | Homo sapiens (human) | 4851 | NOTCH1 |
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| DOID:0111636 | autosomal recessive nonsyndromic deafness 113 | HGNC:31948 | Homo sapiens (human) | 388551 | CEACAM16 |
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| DOID:0111579 | asthma, nasal polyps, and aspirin intolerance | HGNC:9594 | Homo sapiens (human) | 5732 | PTGER2 |
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| DOID:11714 | gestational diabetes | HGNC:21050 | Homo sapiens (human) | 54901 | CDKAL1 |
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| DOID:14004 | thoracic aortic aneurysm | HGNC:7590 | Homo sapiens (human) | 4638 | MYLK |
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| DOID:576 | proteinuria | HGNC:7579 | Homo sapiens (human) | 4627 | MYH9 |
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| DOID:10283 | prostate cancer | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:8778 | Crohn's disease | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:0110790 | hereditary spastic paraplegia 39 | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:10952 | nephritis | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:12132 | granulomatosis with polyangiitis | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:2228 | thrombocytosis | HGNC:7217 | Homo sapiens (human) | 4352 | MPL |
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| DOID:0050774 | rapadilino syndrome | HGNC:9949 | Homo sapiens (human) | 9401 | RECQL4 |
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| DOID:2018 | hyperinsulinism | HGNC:59 | Homo sapiens (human) | 6833 | ABCC8 |
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