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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:0111223 | centronuclear myopathy 1 | HGNC:26190 | Homo sapiens (human) | 64419 | MTMR14 |
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| DOID:678 | progressive supranuclear palsy | HGNC:6893 | Homo sapiens (human) | 4137 | MAPT |
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| DOID:0080199 | colorectal carcinoma | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:0111031 | hemochromatosis type 5 | HGNC:3976 | Homo sapiens (human) | 2495 | FTH1 |
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| DOID:0110122 | Axenfeld-Rieger syndrome type 3 | HGNC:3800 | Homo sapiens (human) | 2296 | FOXC1 |
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| DOID:14330 | Parkinson's disease | HGNC:13586 | Homo sapiens (human) | 25793 | FBXO7 |
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| DOID:12858 | Huntington's disease | HGNC:7957 | Homo sapiens (human) | 4887 | NPY2R |
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| DOID:0111207 | autosomal dominant distal hereditary motor neuronopathy 3 | HGNC:5246 | Homo sapiens (human) | 3315 | HSPB1 |
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| DOID:9256 | colorectal cancer | HGNC:3595 | Homo sapiens (human) | 2195 | FAT1 |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:0111315 | idiopathic generalized epilepsy 14 | HGNC:13818 | Homo sapiens (human) | 57468 | SLC12A5 |
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| DOID:3393 | coronary artery disease | HGNC:6125 | Homo sapiens (human) | 3667 | IRS1 |
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| DOID:13378 | Kawasaki disease | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
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| DOID:5419 | schizophrenia | HGNC:14248 | Homo sapiens (human) | 51586 | MED15 |
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| DOID:0060773 | cleft lip-palate-ectodermal dysplasia syndrome | HGNC:9706 | Homo sapiens (human) | 5818 | NECTIN1 |
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| DOID:0111503 | Li-Fraumeni syndrome 1 | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:1612 | breast cancer | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0080687 | reducing body myopathy 1B | HGNC:3702 | Homo sapiens (human) | 2273 | FHL1 |
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| DOID:0070480 | schwannomatosis 1 | HGNC:11103 | Homo sapiens (human) | 6598 | SMARCB1 |
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| DOID:612 | primary immunodeficiency disease | HGNC:25118 | Homo sapiens (human) | 90268 | OTULIN |
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| DOID:14018 | alcoholic liver cirrhosis | HGNC:8583 | Homo sapiens (human) | 5054 | SERPINE1 |
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| DOID:0110683 | congenital myasthenic syndrome 18 | HGNC:11132 | Homo sapiens (human) | 6616 | SNAP25 |
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| DOID:11054 | urinary bladder cancer | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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| DOID:7147 | ankylosing spondylitis | HGNC:6112 | Homo sapiens (human) | 3654 | IRAK1 |
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| DOID:0080385 | nephrotic syndrome type 11 | HGNC:29914 | Homo sapiens (human) | 57122 | NUP107 |
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