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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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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:399 | tuberculosis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
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| DOID:1059 | intellectual disability | HGNC:6050 | Homo sapiens (human) | 3612 | IMPA1 |
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| DOID:3312 | bipolar disorder | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:0050802 | Ehlers-Danlos syndrome spondylodysplastic type 2 | HGNC:17978 | Homo sapiens (human) | 126792 | B3GALT6 |
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| DOID:12401 | intermittent explosive disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0112222 | developmental and epileptic encephalopathy 88 | HGNC:6970 | Homo sapiens (human) | 4190 | MDH1 |
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| DOID:11702 | dysgammaglobulinemia | HGNC:12572 | Homo sapiens (human) | 7374 | UNG |
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| DOID:783 | end stage renal disease | HGNC:2622 | Homo sapiens (human) | 1558 | CYP2C8 |
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| DOID:0110245 | cataract 38 | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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| DOID:3393 | coronary artery disease | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:0050753 | cerebellar ataxia | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:3385 | bacterial vaginosis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0050581 | brachydactyly | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:9538 | multiple myeloma | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:12177 | common variable immunodeficiency | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:1059 | intellectual disability | HGNC:5996 | Homo sapiens (human) | 11141 | IL1RAPL1 |
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| DOID:9452 | steatotic liver disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:0112349 | hereditary spastic paraplegia 81 | HGNC:29361 | Homo sapiens (human) | 85465 | SELENOI |
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| DOID:0080459 | developmental and epileptic encephalopathy 12 | HGNC:15917 | Homo sapiens (human) | 23236 | PLCB1 |
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| DOID:3717 | gastric adenocarcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0080762 | autosomal recessive limb-girdle muscular dystrophy type 2Z | HGNC:22954 | Homo sapiens (human) | 56983 | POGLUT1 |
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| DOID:11612 | polycystic ovary syndrome | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:13078 | eumycotic mycetoma | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0081120 | Graves ophthalmopathy | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:8970 | subacute sclerosing panencephalitis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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