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GlyTouCan
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
LM-GlycoRepo
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:1612 | breast cancer | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:0111787 | frontometaphyseal dysplasia 2 | HGNC:6859 | Homo sapiens (human) | 6885 | MAP3K7 |
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| DOID:10584 | retinitis pigmentosa | HGNC:34 | Homo sapiens (human) | 24 | ABCA4 |
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| DOID:0111249 | uveal coloboma-cleft lip and palate-intellectual disability | HGNC:16262 | Homo sapiens (human) | 10413 | YAP1 |
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| DOID:12849 | autistic disorder | HGNC:8032 | Homo sapiens (human) | 4915 | NTRK2 |
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| DOID:10003 | sensorineural hearing loss | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:0070059 | autosomal dominant intellectual developmental disorder 29 | HGNC:15573 | Homo sapiens (human) | 26040 | SETBP1 |
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| DOID:418 | systemic scleroderma | HGNC:5974 | Homo sapiens (human) | 3597 | IL13RA1 |
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| DOID:4947 | cholangiocarcinoma | HGNC:3527 | Homo sapiens (human) | 2146 | EZH2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:684 | hepatocellular carcinoma | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:2043 | hepatitis B | HGNC:5439 | Homo sapiens (human) | 3459 | IFNGR1 |
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| DOID:1555 | urticaria | HGNC:1603 | Homo sapiens (human) | 729230 | CCR2 |
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| DOID:6000 | congestive heart failure | HGNC:4396 | Homo sapiens (human) | 2782 | GNB1 |
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| DOID:0070379 | developmental and epileptic encephalopathy 6B | HGNC:10585 | Homo sapiens (human) | 6323 | SCN1A |
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| DOID:8778 | Crohn's disease | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0050562 | West syndrome | HGNC:11444 | Homo sapiens (human) | 6812 | STXBP1 |
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| DOID:0060409 | NFIA-related disorder | HGNC:7784 | Homo sapiens (human) | 4774 | NFIA |
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| DOID:0111054 | von Willebrand's disease 3 | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:8947 | diabetic retinopathy | HGNC:4323 | Homo sapiens (human) | 2739 | GLO1 |
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| DOID:0050646 | distal arthrogryposis | HGNC:7029 | Homo sapiens (human) | 4233 | MET |
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| DOID:0081400 | autosomal dominant distal hereditary motor neuronopathy 11 | HGNC:11273 | Homo sapiens (human) | 6709 | SPTAN1 |
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| DOID:2377 | multiple sclerosis | HGNC:5438 | Homo sapiens (human) | 3458 | IFNG |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:2841 | asthma | HGNC:23631 | Homo sapiens (human) | 387129 | NPSR1 |
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