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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:1324 | lung cancer | HGNC:1964 | Homo sapiens (human) | 1143 | CHRNB4 |
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| DOID:4362 | cervical cancer | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:0050168 | autoimmune polyendocrine syndrome type 2 | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:1059 | intellectual disability | HGNC:10432 | Homo sapiens (human) | 6197 | RPS6KA3 |
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| DOID:2043 | hepatitis B | HGNC:11849 | Homo sapiens (human) | 7098 | TLR3 |
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| DOID:14115 | toxic shock syndrome | HGNC:5233 | Homo sapiens (human) | 3304 | HSPA1B |
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| DOID:0112333 | pontocerebellar hypoplasia type 16 | HGNC:7102 | Homo sapiens (human) | 9562 | MINPP1 |
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| DOID:3121 | gallbladder cancer | HGNC:28611 | Homo sapiens (human) | 253260 | RICTOR |
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| DOID:2841 | asthma | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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| DOID:0111180 | French Canadian Leigh disease | HGNC:15714 | Homo sapiens (human) | 10128 | LRPPRC |
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| DOID:0060838 | isolated microphthalmia 7 | HGNC:4218 | Homo sapiens (human) | 9573 | GDF3 |
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| DOID:0080006 | bone development disease | HGNC:11908 | Homo sapiens (human) | 8792 | TNFRSF11A |
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| DOID:4398 | pustulosis of palm and sole | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:3770 | pulmonary fibrosis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:9778 | irritable bowel syndrome | HGNC:18505 | Homo sapiens (human) | 54894 | RNF43 |
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| DOID:3211 | lysosomal storage disease | HGNC:9251 | Homo sapiens (human) | 5476 | CTSA |
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| DOID:0060203 | amyotrophic lateral sclerosis type 12 | HGNC:17142 | Homo sapiens (human) | 10133 | OPTN |
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| DOID:684 | hepatocellular carcinoma | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:0111649 | ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome | HGNC:1762 | Homo sapiens (human) | 1001 | CDH3 |
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| DOID:0111437 | optic atrophy 7 | HGNC:25382 | Homo sapiens (human) | 84233 | TMEM126A |
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| DOID:11123 | Henoch-Schoenlein purpura | HGNC:6998 | Homo sapiens (human) | 4210 | MEFV |
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| DOID:0080339 | familial erythrocytosis 4 | HGNC:3374 | Homo sapiens (human) | 2034 | EPAS1 |
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| DOID:3070 | high grade glioma | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:0080678 | mucolipidosis III gamma | HGNC:23026 | Homo sapiens (human) | 84572 | GNPTG |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:30348 | Homo sapiens (human) | 55703 | POLR3B |
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