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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:0060610 | megacystis-microcolon-intestinal hypoperistalsis syndrome | HGNC:7590 | Homo sapiens (human) | 4638 | MYLK |
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| DOID:1909 | melanoma | HGNC:1101 | Homo sapiens (human) | 675 | BRCA2 |
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| DOID:0060754 | familial temporal lobe epilepsy 8 | HGNC:4114 | Homo sapiens (human) | 51083 | GAL |
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| DOID:10652 | Alzheimer's disease | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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| DOID:5844 | myocardial infarction | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:6713 | cerebrovascular disease | HGNC:17855 | Homo sapiens (human) | 26035 | GLCE |
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| DOID:1024 | leprosy | HGNC:5331 | Homo sapiens (human) | 64127 | NOD2 |
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| DOID:0090093 | hypogonadotropic hypogonadism 21 with or without anosmia | HGNC:3762 | Homo sapiens (human) | 23767 | FLRT3 |
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| DOID:0080437 | developmental and epileptic encephalopathy 31A | HGNC:2972 | Homo sapiens (human) | 1759 | DNM1 |
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| DOID:0070112 | Niemann-Pick disease type B | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:0050168 | autoimmune polyendocrine syndrome type 2 | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:6713 | cerebrovascular disease | HGNC:10718 | Homo sapiens (human) | 6401 | SELE |
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| DOID:10652 | Alzheimer's disease | HGNC:30654 | Homo sapiens (human) | 54464 | XRN1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:10720 | Homo sapiens (human) | 6402 | SELL |
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| DOID:670 | amphetamine abuse | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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| DOID:0090103 | Huntington's disease-like 1 | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:1612 | breast cancer | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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| DOID:5844 | myocardial infarction | HGNC:610 | Homo sapiens (human) | 345 | APOC3 |
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| DOID:83 | cataract | HGNC:4204 | Homo sapiens (human) | 2651 | GCNT2 |
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| DOID:10825 | essential hypertension | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:43 | Homo sapiens (human) | 6890 | TAP1 |
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| DOID:6000 | congestive heart failure | HGNC:11111 | Homo sapiens (human) | 8243 | SMC1A |
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| DOID:0080188 | chronic myelomonocytic leukemia | HGNC:18318 | Homo sapiens (human) | 171023 | ASXL1 |
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| DOID:0112202 | developmental and epileptic encephalopathy | HGNC:18423 | Homo sapiens (human) | 9681 | DEPDC5 |
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| DOID:1996 | rectum adenocarcinoma | HGNC:11364 | Homo sapiens (human) | 6774 | STAT3 |
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