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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:0110242 | cataract 13 with adult i phenotype | HGNC:4204 | Homo sapiens (human) | 2651 | GCNT2 |
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| DOID:12554 | hemolytic-uremic syndrome | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:30308 | Homo sapiens (human) | 56963 | RGMA |
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| DOID:0080414 | developmental and epileptic encephalopathy 15 | HGNC:10866 | Homo sapiens (human) | 6487 | ST3GAL3 |
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| DOID:2224 | essential thrombocythemia | HGNC:12663 | Homo sapiens (human) | 7412 | VCAM1 |
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| DOID:1459 | hypothyroidism | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:0111393 | mucopolysaccharidosis type IIIC | HGNC:26527 | Homo sapiens (human) | 138050 | HGSNAT |
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| DOID:5844 | myocardial infarction | HGNC:10661 | Homo sapiens (human) | 6385 | SDC4 |
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| DOID:7148 | rheumatoid arthritis | HGNC:8638 | Homo sapiens (human) | 8850 | KAT2B |
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| DOID:9976 | heroin dependence | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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| DOID:10808 | gastric ulcer | HGNC:5391 | Homo sapiens (human) | 3425 | IDUA |
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| DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:850 | lung disease | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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| DOID:0080665 | warfarin resistance | HGNC:2623 | Homo sapiens (human) | 1559 | CYP2C9 |
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| DOID:8725 | vascular dementia | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:12803 | Sly syndrome | HGNC:4696 | Homo sapiens (human) | 2990 | GUSB |
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| DOID:612 | primary immunodeficiency disease | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0060001 | withdrawal disorder | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:8398 | osteoarthritis | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12538 | Homo sapiens (human) | 54578 | UGT1A6 |
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| DOID:0080488 | mucolipidosis | HGNC:29670 | Homo sapiens (human) | 79158 | GNPTAB |
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| DOID:0080563 | congenital disorder of glycosylation Ik | HGNC:18294 | Homo sapiens (human) | 56052 | ALG1 |
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| DOID:9119 | acute myeloid leukemia | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:14330 | Parkinson's disease | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:0080199 | colorectal carcinoma | HGNC:4554 | Homo sapiens (human) | 2877 | GPX2 |
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