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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:14264 | benign neonatal seizures | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:0110980 | Joubert syndrome 1 | HGNC:21474 | Homo sapiens (human) | 56623 | INPP5E |
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| DOID:653 | purine-pyrimidine metabolic disorder | HGNC:7892 | Homo sapiens (human) | 4860 | PNP |
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| DOID:0080932 | primary localized cutaneous amyloidosis 3 | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
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| DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:2679 | dysembryoplastic neuroepithelial tumor | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:3572 | intracranial sinus thrombosis | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:4483 | rhinitis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
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| DOID:10608 | celiac disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:11212 | hydrophthalmos | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:1350 | paranasal sinus benign neoplasm | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:1612 | breast cancer | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:1240 | leukemia | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:1612 | breast cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:417 | autoimmune disease | HGNC:18187 | Homo sapiens (human) | 54414 | SIAE |
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| 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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