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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:1059 | intellectual disability | HGNC:18683 | Homo sapiens (human) | 9775 | EIF4A3 |
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| DOID:1793 | pancreatic cancer | HGNC:18683 | Homo sapiens (human) | 9775 | EIF4A3 |
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| DOID:9970 | obesity | HGNC:19166 | Homo sapiens (human) | 9779 | TBC1D5 |
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| DOID:0111576 | dehydrated hereditary stomatocytosis 1 | HGNC:28993 | Homo sapiens (human) | 9780 | PIEZO1 |
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| DOID:0050580 | hereditary lymphedema | HGNC:28993 | Homo sapiens (human) | 9780 | PIEZO1 |
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| DOID:0060212 | amyotrophic lateral sclerosis type 21 | HGNC:6912 | Homo sapiens (human) | 9782 | MATR3 |
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| DOID:0112141 | retinitis pigmentosa 84 | HGNC:17211 | Homo sapiens (human) | 9785 | DHX38 |
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| DOID:0081301 | intellectual developmental disorder with ocular anomalies and distinctive facial features | HGNC:20443 | Homo sapiens (human) | 9788 | MTSS1 |
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| DOID:0060060 | non-Hodgkin lymphoma | HGNC:20443 | Homo sapiens (human) | 9788 | MTSS1 |
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| DOID:0111230 | congenital muscular dystrophy-dystroglycanopathy type A11 | MGI:2145517 | Mus musculus (house mouse) | 97884 | B3galnt2 |
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| DOID:14330 | Parkinson's disease | HGNC:28962 | Homo sapiens (human) | 9789 | SPCS2 |
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| DOID:0080661 | nonsyndromic aplasia cutis congenita | HGNC:23505 | Homo sapiens (human) | 9790 | BMS1 |
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| DOID:0111507 | Lenz-Majewski hyperostotic dwarfism | HGNC:9587 | Homo sapiens (human) | 9791 | PTDSS1 |
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| DOID:12387 | nephrogenic diabetes insipidus | HGNC:16867 | Homo sapiens (human) | 9810 | RNF40 |
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| DOID:1682 | congenital heart disease | HGNC:16867 | Homo sapiens (human) | 9810 | RNF40 |
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| DOID:8947 | diabetic retinopathy | HGNC:23177 | Homo sapiens (human) | 9817 | KEAP1 |
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| DOID:5199 | ureteral obstruction | HGNC:23177 | Homo sapiens (human) | 9817 | KEAP1 |
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| DOID:2797 | idiopathic interstitial pneumonia | HGNC:23177 | Homo sapiens (human) | 9817 | KEAP1 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:23177 | Homo sapiens (human) | 9817 | KEAP1 |
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| DOID:9675 | pulmonary emphysema | HGNC:23177 | Homo sapiens (human) | 9817 | KEAP1 |
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| DOID:3121 | gallbladder cancer | HGNC:23177 | Homo sapiens (human) | 9817 | KEAP1 |
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| DOID:783 | end stage renal disease | HGNC:23177 | Homo sapiens (human) | 9817 | KEAP1 |
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| DOID:0060241 | 3-M syndrome | HGNC:21024 | Homo sapiens (human) | 9820 | CUL7 |
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| DOID:1612 | breast cancer | HGNC:15574 | Homo sapiens (human) | 9821 | RB1CC1 |
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| DOID:10941 | intracranial aneurysm | HGNC:21726 | Homo sapiens (human) | 9828 | ARHGEF17 |
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