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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:0080046 | Stickler syndrome | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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| DOID:1612 | breast cancer | HGNC:2593 | Homo sapiens (human) | 1586 | CYP17A1 |
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| DOID:0050073 | invasive aspergillosis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0060462 | Desbuquois dysplasia | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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| DOID:0080322 | polycystic kidney disease | HGNC:20266 | Homo sapiens (human) | 29880 | ALG5 |
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| DOID:9884 | muscular dystrophy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:8577 | ulcerative colitis | HGNC:10720 | Homo sapiens (human) | 6402 | SELL |
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| DOID:0112380 | muscular dystrophy-dystroglycanopathy type B2 | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0080138 | multiple congenital anomalies-hypotonia-seizures syndrome 1 | HGNC:8967 | Homo sapiens (human) | 23556 | PIGN |
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| DOID:0080559 | congenital disorder of glycosylation Ig | HGNC:19358 | Homo sapiens (human) | 79087 | ALG12 |
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| DOID:0080016 | spina bifida | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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| DOID:6846 | familial melanoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:12930 | dilated cardiomyopathy | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:9268 | glycine encephalopathy | HGNC:473 | Homo sapiens (human) | 275 | AMT |
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| DOID:4586 | familial meningioma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:12554 | hemolytic-uremic syndrome | HGNC:24338 | Homo sapiens (human) | 29071 | C1GALT1C1 |
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| DOID:2893 | cervix carcinoma | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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| DOID:0050731 | vitamin B12 deficiency | HGNC:4013 | Homo sapiens (human) | 2524 | FUT2 |
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| DOID:83 | cataract | HGNC:4204 | Homo sapiens (human) | 2651 | GCNT2 |
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| DOID:3454 | brain infarction | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:0080464 | developmental and epileptic encephalopathy 53 | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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| DOID:4988 | alcoholic pancreatitis | HGNC:12539 | Homo sapiens (human) | 54577 | UGT1A7 |
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| DOID:0060577 | 3MC syndrome 3 | HGNC:2220 | Homo sapiens (human) | 10584 | COLEC10 |
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| DOID:0080950 | alopecia-mental retardation syndrome 4 | HGNC:6708 | Homo sapiens (human) | 4047 | LSS |
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