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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
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Repository for lectin-assisted multimodality data
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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:0050663 | Bethlem myopathy | HGNC:2188 | Homo sapiens (human) | 1303 | COL12A1 |
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| DOID:9562 | primary ciliary dyskinesia | HGNC:12760 | Homo sapiens (human) | 54014 | BRWD1 |
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| DOID:0070394 | developmental and epileptic encephalopathy 108 | HGNC:19036 | Homo sapiens (human) | 23031 | MAST3 |
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| DOID:0080267 | autosomal dominant nonsyndromic deafness 71 | HGNC:2938 | Homo sapiens (human) | 23312 | DMXL2 |
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| DOID:0112155 | inflammatory bowel disease 29 | HGNC:25599 | Homo sapiens (human) | 55765 | INAVA |
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| DOID:0060211 | amyotrophic lateral sclerosis type 20 | HGNC:5031 | Homo sapiens (human) | 3178 | HNRNPA1 |
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| DOID:0081234 | autosomal recessive intellectual developmental disorder 75 | HGNC:16491 | Homo sapiens (human) | 55367 | PIDD1 |
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| DOID:0112105 | X-linked parkinsonism-spasticity syndrome | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:0112314 | brain small vessel disease 2 | HGNC:2203 | Homo sapiens (human) | 1284 | COL4A2 |
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| DOID:14766 | renal agenesis | HGNC:6144 | Homo sapiens (human) | 8516 | ITGA8 |
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| DOID:0111542 | familial expansile osteolysis | HGNC:11908 | Homo sapiens (human) | 8792 | TNFRSF11A |
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| DOID:1441 | autosomal dominant cerebellar ataxia | HGNC:7952 | Homo sapiens (human) | 4884 | NPTX1 |
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| DOID:0110340 | osteogenesis imperfecta type 4 | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:0060193 | amyotrophic lateral sclerosis type 1 | HGNC:2711 | Homo sapiens (human) | 1639 | DCTN1 |
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| DOID:0080952 | AMED syndrome | HGNC:253 | Homo sapiens (human) | 128 | ADH5 |
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| DOID:0110262 | cataract 45 | HGNC:23801 | Homo sapiens (human) | 23094 | SIPA1L3 |
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| DOID:0080451 | developmental and epileptic encephalopathy 29 | HGNC:20 | Homo sapiens (human) | 16 | AARS1 |
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| DOID:0060774 | congenital diarrhea | HGNC:13635 | Homo sapiens (human) | 83483 | PLVAP |
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| DOID:0060453 | Reis-Bucklers corneal dystrophy | HGNC:11771 | Homo sapiens (human) | 7045 | TGFBI |
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| DOID:0080588 | agammaglobulinemia 5 | HGNC:19027 | Homo sapiens (human) | 56262 | LRRC8A |
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| DOID:0090048 | dystonia 16 | HGNC:9438 | Homo sapiens (human) | 8575 | PRKRA |
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| DOID:0111908 | thrombophilia due to thrombomodulin defect | HGNC:11784 | Homo sapiens (human) | 7056 | THBD |
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| DOID:0060301 | type I complement component 8 deficiency | HGNC:1352 | Homo sapiens (human) | 731 | C8A |
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| DOID:0080421 | developmental and epileptic encephalopathy 11 | HGNC:10588 | Homo sapiens (human) | 6326 | SCN2A |
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| DOID:0060937 | dystonia 30 | HGNC:14584 | Homo sapiens (human) | 64601 | VPS16 |
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