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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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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:11476 | osteoporosis | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:3770 | pulmonary fibrosis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3770 | pulmonary fibrosis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0050855 | renal fibrosis | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:0050545 | visceral heterotaxy | HGNC:18292 | Homo sapiens (human) | 55997 | CFC1 |
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| DOID:3211 | lysosomal storage disease | HGNC:4879 | Homo sapiens (human) | 3074 | HEXB |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0111677 | familial benign fleck retina | HGNC:9038 | Homo sapiens (human) | 5322 | PLA2G5 |
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| DOID:9970 | obesity | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:0060158 | acquired metabolic disease | HGNC:30802 | Homo sapiens (human) | 57104 | PNPLA2 |
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| DOID:9828 | neonatal abstinence syndrome | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0060074 | ductal carcinoma in situ | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:3021 | acute kidney failure | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:2154 | nephroblastoma | HGNC:5467 | Homo sapiens (human) | 3482 | IGF2R |
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| DOID:1826 | epilepsy | HGNC:1400 | Homo sapiens (human) | 9254 | CACNA2D2 |
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| DOID:438 | autoimmune disease of the nervous system | HGNC:418 | Homo sapiens (human) | 230 | ALDOC |
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| DOID:0050453 | lissencephaly | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:114 | heart disease | HGNC:8976 | Homo sapiens (human) | 5291 | PIK3CB |
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| DOID:8805 | intermediate coronary syndrome | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:853 | polymyalgia rheumatica | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:6000 | congestive heart failure | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:10964 | cholesteatoma of middle ear | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0110669 | congenital myasthenic syndrome 14 | HGNC:23159 | Homo sapiens (human) | 85365 | ALG2 |
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| DOID:0111110 | maturity-onset diabetes of the young type 13 | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:83 | cataract | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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