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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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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:3070 | high grade glioma | HGNC:1101 | Homo sapiens (human) | 675 | BRCA2 |
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| DOID:8761 | acute megakaryocytic leukemia | HGNC:14334 | Homo sapiens (human) | 57591 | MRTFA |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:1960 | Homo sapiens (human) | 1139 | CHRNA7 |
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| DOID:10003 | sensorineural hearing loss | HGNC:11877 | Homo sapiens (human) | 64699 | TMPRSS3 |
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| DOID:4450 | renal cell carcinoma | HGNC:1324 | Homo sapiens (human) | 721 | C4B |
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| DOID:684 | hepatocellular carcinoma | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0111096 | Fanconi anemia complementation group O | HGNC:9820 | Homo sapiens (human) | 5889 | RAD51C |
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| DOID:0111989 | immunodeficiency 35 | HGNC:12440 | Homo sapiens (human) | 7297 | TYK2 |
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| DOID:0080137 | multiple endocrine neoplasia type 4 | HGNC:1785 | Homo sapiens (human) | 1027 | CDKN1B |
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| DOID:0070294 | primary autosomal recessive microcephaly 10 | HGNC:15807 | Homo sapiens (human) | 63925 | ZNF335 |
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| DOID:0050581 | brachydactyly | HGNC:5136 | Homo sapiens (human) | 3239 | HOXD13 |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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| DOID:3393 | coronary artery disease | HGNC:94 | Homo sapiens (human) | 39 | ACAT2 |
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| DOID:2738 | pseudoxanthoma elasticum | HGNC:11180 | Homo sapiens (human) | 6648 | SOD2 |
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| DOID:0111740 | X-linked deafness 6 | HGNC:2208 | Homo sapiens (human) | 1288 | COL4A6 |
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| DOID:0070007 | Seckel syndrome 1 | HGNC:882 | Homo sapiens (human) | 545 | ATR |
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| DOID:0050589 | inflammatory bowel disease | HGNC:437 | Homo sapiens (human) | 248 | ALPI |
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| DOID:0080628 | alopecia-mental retardation syndrome 1 | HGNC:349 | Homo sapiens (human) | 197 | AHSG |
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| DOID:1612 | breast cancer | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:9834 | hyperopia | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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| DOID:0080382 | nephrotic syndrome type 3 | HGNC:17175 | Homo sapiens (human) | 51196 | PLCE1 |
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| DOID:4428 | dyslexia | HGNC:21493 | Homo sapiens (human) | 161582 | DNAAF4 |
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| DOID:12306 | vitiligo | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:12361 | Graves' disease | HGNC:1323 | Homo sapiens (human) | 720 | C4A |
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| DOID:7148 | rheumatoid arthritis | HGNC:19100 | Homo sapiens (human) | 149233 | IL23R |
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