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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:0050156 | idiopathic pulmonary fibrosis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:557 | kidney disease | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:2596 | Homo sapiens (human) | 1544 | CYP1A2 |
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| DOID:0080672 | fibrochondrogenesis 1 | HGNC:2186 | Homo sapiens (human) | 1301 | COL11A1 |
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| DOID:5844 | myocardial infarction | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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| DOID:2043 | hepatitis B | HGNC:15633 | Homo sapiens (human) | 54106 | TLR9 |
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| DOID:0080404 | orofacial cleft 11 | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:12894 | Sjogren's syndrome | HGNC:11365 | Homo sapiens (human) | 6775 | STAT4 |
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| DOID:0110810 | hereditary spastic paraplegia 5A | HGNC:2652 | Homo sapiens (human) | 9420 | CYP7B1 |
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| DOID:3602 | toxic encephalopathy | HGNC:5465 | Homo sapiens (human) | 3480 | IGF1R |
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| DOID:6419 | tetralogy of Fallot | HGNC:8004 | Homo sapiens (human) | 8829 | NRP1 |
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| DOID:12960 | acrocephalosyndactylia | HGNC:3688 | Homo sapiens (human) | 2260 | FGFR1 |
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| DOID:2349 | arteriosclerosis | HGNC:3467 | Homo sapiens (human) | 2099 | ESR1 |
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| DOID:0050458 | juvenile myelomonocytic leukemia | HGNC:1541 | Homo sapiens (human) | 867 | CBL |
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| DOID:2377 | multiple sclerosis | HGNC:4077 | Homo sapiens (human) | 2556 | GABRA3 |
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| DOID:6000 | congestive heart failure | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:0070242 | primary coenzyme Q10 deficiency 5 | HGNC:25302 | Homo sapiens (human) | 57017 | COQ9 |
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| DOID:0080345 | blepharocheilodontic syndrome 1 | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:11758 | iron deficiency anemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:7693 | abdominal aortic aneurysm | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:0080456 | developmental and epileptic encephalopathy 46 | HGNC:4588 | Homo sapiens (human) | 2906 | GRIN2D |
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| DOID:0050477 | Liddle syndrome | HGNC:10599 | Homo sapiens (human) | 6337 | SCNN1A |
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| DOID:9074 | systemic lupus erythematosus | HGNC:5232 | Homo sapiens (human) | 3303 | HSPA1A |
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| DOID:0060257 | dyschromatosis symmetrica hereditaria | HGNC:225 | Homo sapiens (human) | 103 | ADAR |
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