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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:0060224 | atrial fibrillation | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:9970 | obesity | HGNC:2606 | Homo sapiens (human) | 1594 | CYP27B1 |
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| DOID:2626 | choroid plexus papilloma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:10223 | dermatomyositis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:13544 | low tension glaucoma | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0081097 | Rafiq syndrome | HGNC:6823 | Homo sapiens (human) | 11253 | MAN1B1 |
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| DOID:1485 | cystic fibrosis | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:4947 | cholangiocarcinoma | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:0112251 | Ghosal hematodiaphyseal syndrome | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:0111933 | phosphoglycerate kinase 1 deficiency | HGNC:8896 | Homo sapiens (human) | 5230 | PGK1 |
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| DOID:0081180 | autosomal recessive intellectual developmental disorder 12 | HGNC:10866 | Homo sapiens (human) | 6487 | ST3GAL3 |
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| DOID:3393 | coronary artery disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:7148 | rheumatoid arthritis | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:0112343 | hereditary spastic paraplegia 82 | HGNC:8756 | Homo sapiens (human) | 5833 | PCYT2 |
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| DOID:1380 | endometrial cancer | HGNC:8905 | Homo sapiens (human) | 5236 | PGM1 |
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| DOID:1580 | diffuse scleroderma | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:12361 | Graves' disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0080941 | acquired angioedema | HGNC:12823 | Homo sapiens (human) | 7512 | XPNPEP2 |
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| DOID:13809 | familial combined hyperlipidemia | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:6196 | reactive arthritis | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0060445 | congenital stromal corneal dystrophy | HGNC:2705 | Homo sapiens (human) | 1634 | DCN |
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| DOID:3526 | cerebral infarction | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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| DOID:0060774 | congenital diarrhea | HGNC:16526 | Homo sapiens (human) | 51703 | ACSL5 |
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| DOID:13564 | aspergillosis | HGNC:11847 | Homo sapiens (human) | 7096 | TLR1 |
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| DOID:9256 | colorectal cancer | HGNC:19877 | Homo sapiens (human) | 79695 | GALNT12 |
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