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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:0111819 | syndactyly type 5 | HGNC:5136 | Homo sapiens (human) | 3239 | HOXD13 |
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| DOID:0081237 | acromesomelic dysplasia-3 | HGNC:1077 | Homo sapiens (human) | 658 | BMPR1B |
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| DOID:3652 | Leigh disease | HGNC:7458 | Homo sapiens (human) | 4537 | ND3 |
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| DOID:0050700 | cardiomyopathy | HGNC:7150 | Homo sapiens (human) | 23417 | MLYCD |
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| DOID:0111510 | Marshall syndrome | HGNC:2186 | Homo sapiens (human) | 1301 | COL11A1 |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:12009 | Homo sapiens (human) | 7167 | TPI1 |
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| DOID:0060298 | complement component 4b deficiency | HGNC:1324 | Homo sapiens (human) | 721 | C4B |
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| DOID:9975 | cocaine dependence | HGNC:4070 | Homo sapiens (human) | 2550 | GABBR1 |
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| DOID:0080932 | primary localized cutaneous amyloidosis 3 | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
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| DOID:0080987 | Ehlers-Danlos syndrome periodontal type 2 | HGNC:1247 | Homo sapiens (human) | 716 | C1S |
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| DOID:9970 | obesity | HGNC:2606 | Homo sapiens (human) | 1594 | CYP27B1 |
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| DOID:8947 | diabetic retinopathy | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:0070296 | primary autosomal recessive microcephaly | HGNC:24502 | Homo sapiens (human) | 284403 | WDR62 |
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| DOID:4947 | cholangiocarcinoma | HGNC:22950 | Homo sapiens (human) | 80243 | PREX2 |
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| DOID:3393 | coronary artery disease | HGNC:2548 | Homo sapiens (human) | 8029 | CUBN |
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| DOID:326 | ischemia | HGNC:10618 | Homo sapiens (human) | 6347 | CCL2 |
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| DOID:13096 | Sneddon syndrome | HGNC:1839 | Homo sapiens (human) | 51816 | ADA2 |
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| DOID:2018 | hyperinsulinism | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:12849 | autistic disorder | HGNC:8978 | Homo sapiens (human) | 5294 | PIK3CG |
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| DOID:106 | pleural tuberculosis | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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| DOID:0112000 | immunodeficiency 34 | HGNC:2578 | Homo sapiens (human) | 1536 | CYBB |
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| DOID:7148 | rheumatoid arthritis | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:0111373 | familial progressive hyperpigmentation with or without hypopigmentation | HGNC:6343 | Homo sapiens (human) | 4254 | KITLG |
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| DOID:11981 | morbid obesity | HGNC:8032 | Homo sapiens (human) | 4915 | NTRK2 |
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| DOID:0070451 | mitochondrial DNA depletion syndrome 20 | HGNC:6600 | Homo sapiens (human) | 3980 | LIG3 |
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