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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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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:1470 | major depressive disorder | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:0080301 | atypical hemolytic-uremic syndrome | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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| DOID:0111961 | immunodeficiency 26 | HGNC:9413 | Homo sapiens (human) | 5591 | PRKDC |
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| DOID:3025 | acinar cell carcinoma | HGNC:583 | Homo sapiens (human) | 324 | APC |
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| DOID:12361 | Graves' disease | HGNC:4951 | Homo sapiens (human) | 3125 | HLA-DRB3 |
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| DOID:10283 | prostate cancer | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
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| DOID:0070030 | ITM2B-related cerebral amyloid angiopathy 2 | HGNC:6174 | Homo sapiens (human) | 9445 | ITM2B |
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| DOID:8947 | diabetic retinopathy | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:0112024 | non-syndromic X-linked intellectual disability 58 | HGNC:11854 | Homo sapiens (human) | 7102 | TSPAN7 |
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| DOID:1307 | dementia | HGNC:12666 | Homo sapiens (human) | 7415 | VCP |
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| DOID:1115 | sarcoma | HGNC:21350 | Homo sapiens (human) | 8050 | PDHX |
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| DOID:2513 | basal cell carcinoma | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:9620 | vesicoureteral reflux | HGNC:5438 | Homo sapiens (human) | 3458 | IFNG |
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| DOID:3312 | bipolar disorder | HGNC:4586 | Homo sapiens (human) | 2904 | GRIN2B |
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| DOID:9240 | erythromelalgia | HGNC:10597 | Homo sapiens (human) | 6335 | SCN9A |
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| DOID:7188 | autoimmune thyroiditis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:12849 | autistic disorder | HGNC:3287 | Homo sapiens (human) | 1977 | EIF4E |
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| DOID:3883 | Lynch syndrome | HGNC:11634 | Homo sapiens (human) | 6925 | TCF4 |
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| DOID:0110458 | dilated cardiomyopathy 1BB | HGNC:3049 | Homo sapiens (human) | 1829 | DSG2 |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:6026 | Homo sapiens (human) | 3577 | CXCR1 |
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| DOID:1588 | thrombocytopenia | HGNC:10618 | Homo sapiens (human) | 6347 | CCL2 |
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| DOID:2987 | familial mediterranean fever | HGNC:2637 | Homo sapiens (human) | 1576 | CYP3A4 |
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| DOID:12971 | hereditary spherocytosis | HGNC:11027 | Homo sapiens (human) | 6521 | SLC4A1 |
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| DOID:0060903 | thrombosis | HGNC:7173 | Homo sapiens (human) | 4314 | MMP3 |
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| DOID:0110374 | retinitis pigmentosa 68 | HGNC:29326 | Homo sapiens (human) | 57709 | SLC7A14 |
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