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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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Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:3393 | coronary artery disease | HGNC:22393 | Homo sapiens (human) | 339479 | BRINP3 |
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| DOID:0110176 | Charcot-Marie-Tooth disease axonal type 2X | HGNC:11226 | Homo sapiens (human) | 80208 | SPG11 |
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| DOID:12849 | autistic disorder | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:2841 | asthma | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:8499 | night blindness | HGNC:10024 | Homo sapiens (human) | 6017 | RLBP1 |
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| DOID:0070074 | autosomal dominant intellectual developmental disorder 44 | HGNC:12303 | Homo sapiens (human) | 7204 | TRIO |
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| DOID:0060058 | lymphoma | HGNC:1919 | Homo sapiens (human) | 1108 | CHD4 |
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| DOID:1984 | rectal benign neoplasm | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:12995 | conduct disorder | HGNC:644 | Homo sapiens (human) | 367 | AR |
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| DOID:9256 | colorectal cancer | HGNC:19877 | Homo sapiens (human) | 79695 | GALNT12 |
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| DOID:216 | dental caries | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:7739 | Homo sapiens (human) | 4747 | NEFL |
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| DOID:0081385 | ataxia-telangiectasia-like disorder-2 | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:0014667 | disease of metabolism | HGNC:11828 | Homo sapiens (human) | 9414 | TJP2 |
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| DOID:0050778 | Meckel syndrome | HGNC:19181 | Homo sapiens (human) | 9928 | KIF14 |
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| DOID:0070067 | White-Sutton syndrome | HGNC:18801 | Homo sapiens (human) | 23126 | POGZ |
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| DOID:0081156 | common variable immunodeficiency 14 | HGNC:21729 | Homo sapiens (human) | 359948 | IRF2BP2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:24308 | Homo sapiens (human) | 81037 | CLPTM1L |
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| DOID:0080253 | Meckel syndrome 13 | HGNC:28128 | Homo sapiens (human) | 84314 | TMEM107 |
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| DOID:11555 | Fuchs' endothelial dystrophy | HGNC:11634 | Homo sapiens (human) | 6925 | TCF4 |
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| DOID:0080953 | amelogenesis imperfecta type 1J | HGNC:14376 | Homo sapiens (human) | 93650 | ACP4 |
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| DOID:10892 | hypospadias | HGNC:11285 | Homo sapiens (human) | 6716 | SRD5A2 |
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| DOID:0050807 | Kahrizi syndrome | HGNC:25812 | Homo sapiens (human) | 79644 | SRD5A3 |
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| DOID:14115 | toxic shock syndrome | HGNC:10801 | Homo sapiens (human) | 6439 | SFTPB |
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| DOID:9505 | cannabis abuse | HGNC:3025 | Homo sapiens (human) | 1815 | DRD4 |
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