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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:0050811 | congenital adrenal hyperplasia | HGNC:2600 | Homo sapiens (human) | 1589 | CYP21A2 |
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| DOID:14067 | Plasmodium falciparum malaria | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:8947 | diabetic retinopathy | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:13564 | aspergillosis | HGNC:24355 | Homo sapiens (human) | 51267 | CLEC1A |
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| DOID:0080736 | Ehlers-Danlos syndrome musculocontractural type 1 | HGNC:24464 | Homo sapiens (human) | 113189 | CHST14 |
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| DOID:635 | acquired immunodeficiency syndrome | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
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| DOID:3450 | cutaneous Paget's disease | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:8778 | Crohn's disease | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:11650 | bronchopulmonary dysplasia | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:0081331 | glycogen storage disease Ic | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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| 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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