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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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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:0112370 | Coffin-Siris syndrome 12 | HGNC:4332 | Homo sapiens (human) | 29998 | BICRA |
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| DOID:0060940 | dystonia 33 | HGNC:9437 | Homo sapiens (human) | 5610 | EIF2AK2 |
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| DOID:3805 | porokeratosis | HGNC:7529 | Homo sapiens (human) | 4597 | MVD |
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| DOID:0090052 | dystonia 24 | HGNC:14004 | Homo sapiens (human) | 63982 | ANO3 |
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| DOID:612 | primary immunodeficiency disease | HGNC:11491 | Homo sapiens (human) | 6850 | SYK |
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| DOID:0080419 | developmental and epileptic encephalopathy 50 | HGNC:1424 | Homo sapiens (human) | 790 | CAD |
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| DOID:0111067 | congenital bile acid synthesis defect 6 | HGNC:120 | Homo sapiens (human) | 8309 | ACOX2 |
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| DOID:0070128 | congenital nongoitrous hypothyroidism 6 | HGNC:11796 | Homo sapiens (human) | 7067 | THRA |
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| DOID:3144 | cutis laxa | HGNC:6714 | Homo sapiens (human) | 4052 | LTBP1 |
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| DOID:0081181 | autosomal recessive intellectual developmental disorder 5 | HGNC:25994 | Homo sapiens (human) | 54888 | NSUN2 |
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| DOID:1338 | congenital dyserythropoietic anemia | HGNC:9804 | Homo sapiens (human) | 29127 | RACGAP1 |
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| DOID:0060210 | amyotrophic lateral sclerosis type 19 | HGNC:3432 | Homo sapiens (human) | 2066 | ERBB4 |
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| DOID:0060308 | autosomal recessive intellectual developmental disorder | HGNC:12017 | Homo sapiens (human) | 7175 | TPR |
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| DOID:0110297 | autosomal recessive limb-girdle muscular dystrophy type 2K | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0112266 | nephrotic syndrome type 23 | HGNC:15734 | Homo sapiens (human) | 55243 | KIRREL1 |
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| DOID:0060292 | X-linked chondrodysplasia punctata 1 | HGNC:719 | Homo sapiens (human) | 415 | ARSL |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4456 | Homo sapiens (human) | 2820 | GPD2 |
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| DOID:0080254 | orofaciodigital syndrome XVI | HGNC:28128 | Homo sapiens (human) | 84314 | TMEM107 |
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| DOID:0080315 | megalencephalic leukoencephalopathy with subcortical cysts | HGNC:637 | Homo sapiens (human) | 361 | AQP4 |
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| DOID:0081023 | retinal cone dystrophy 4 | HGNC:20202 | Homo sapiens (human) | 93589 | CACNA2D4 |
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| DOID:0080669 | posterior polymorphous corneal dystrophy 4 | HGNC:2799 | Homo sapiens (human) | 79977 | GRHL2 |
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| DOID:0110373 | retinitis pigmentosa 61 | HGNC:12605 | Homo sapiens (human) | 7401 | CLRN1 |
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| DOID:0111131 | focal segmental glomerulosclerosis 6 | HGNC:7599 | Homo sapiens (human) | 4643 | MYO1E |
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| DOID:11476 | osteoporosis | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:0050902 | medulloblastoma | HGNC:2514 | Homo sapiens (human) | 1499 | CTNNB1 |
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