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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:0060230 | basal ganglia calcification | HGNC:8800 | Homo sapiens (human) | 5155 | PDGFB |
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| DOID:0111983 | immunodeficiency 52 | HGNC:18874 | Homo sapiens (human) | 27040 | LAT |
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| DOID:0111110 | maturity-onset diabetes of the young type 13 | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:0060558 | lethal congenital contracture syndrome | HGNC:29514 | Homo sapiens (human) | 342035 | GLDN |
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| DOID:0080282 | developmental and epileptic encephalopathy 56 | HGNC:12852 | Homo sapiens (human) | 7532 | YWHAG |
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| DOID:0111777 | 46,XY sex reversal 2 | HGNC:7960 | Homo sapiens (human) | 190 | NR0B1 |
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| DOID:0060902 | Norman-Roberts syndrome | HGNC:9957 | Homo sapiens (human) | 5649 | RELN |
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| DOID:0060286 | combined oxidative phosphorylation deficiency | HGNC:26223 | Homo sapiens (human) | 79736 | TEFM |
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| DOID:0080773 | delta beta-thalassemia | HGNC:4827 | Homo sapiens (human) | 3043 | HBB |
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| DOID:0080673 | fibrochondrogenesis 2 | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:0050675 | Birk-Barel syndrome | HGNC:6283 | Homo sapiens (human) | 51305 | KCNK9 |
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| DOID:0070281 | primary autosomal recessive microcephaly 19 | HGNC:2232 | Homo sapiens (human) | 9276 | COPB2 |
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| DOID:0081268 | pulmonary venoocclusive disease 1 | HGNC:1078 | Homo sapiens (human) | 659 | BMPR2 |
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| DOID:0112349 | hereditary spastic paraplegia 81 | HGNC:29361 | Homo sapiens (human) | 85465 | SELENOI |
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| DOID:14004 | thoracic aortic aneurysm | HGNC:25835 | Homo sapiens (human) | 79875 | THSD4 |
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| DOID:0111167 | Dyggve-Melchior-Clausen disease | HGNC:21317 | Homo sapiens (human) | 54808 | DYM |
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| DOID:0111386 | inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3 | HGNC:5031 | Homo sapiens (human) | 3178 | HNRNPA1 |
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| DOID:6364 | migraine | HGNC:19439 | Homo sapiens (human) | 338567 | KCNK18 |
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| DOID:2394 | ovarian cancer | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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| DOID:0111369 | hyperalphalipoproteinemia 1 | HGNC:1869 | Homo sapiens (human) | 1071 | CETP |
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| DOID:0110015 | age related macular degeneration 2 | HGNC:34 | Homo sapiens (human) | 24 | ABCA4 |
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| DOID:0081003 | Cowden syndrome 7 | HGNC:10702 | Homo sapiens (human) | 10483 | SEC23B |
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| DOID:0081210 | autosomal recessive intellectual developmental disorder 46 | HGNC:7680 | Homo sapiens (human) | 3340 | NDST1 |
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| DOID:0070251 | X-linked Emery-Dreifuss muscular dystrophy 6 | HGNC:3702 | Homo sapiens (human) | 2273 | FHL1 |
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| DOID:0081290 | Antley-Bixler syndrome without disordered steroidogenesis | HGNC:3689 | Homo sapiens (human) | 2263 | FGFR2 |
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