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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▲ |
|---|---|---|---|---|---|---|---|---|
| DOID:0080081 | nonsyndromic congenital nail disorder 3 | HGNC:9060 | Homo sapiens (human) | 5333 | PLCD1 |
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| DOID:12120 | pulmonary alveolar proteinosis | HGNC:10802 | Homo sapiens (human) | 6440 | SFTPC |
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| DOID:0110219 | Brugada syndrome 2 | HGNC:28956 | Homo sapiens (human) | 23171 | GPD1L |
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| DOID:0050647 | Arts syndrome | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:0080558 | congenital disorder of glycosylation If | HGNC:7207 | Homo sapiens (human) | 9526 | MPDU1 |
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| DOID:0080046 | Stickler syndrome | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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| DOID:0060462 | Desbuquois dysplasia | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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| DOID:0080322 | polycystic kidney disease | HGNC:20266 | Homo sapiens (human) | 29880 | ALG5 |
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| DOID:0112380 | muscular dystrophy-dystroglycanopathy type B2 | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0080138 | multiple congenital anomalies-hypotonia-seizures syndrome 1 | HGNC:8967 | Homo sapiens (human) | 23556 | PIGN |
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| DOID:0080559 | congenital disorder of glycosylation Ig | HGNC:19358 | Homo sapiens (human) | 79087 | ALG12 |
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| DOID:6846 | familial melanoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:4586 | familial meningioma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:12554 | hemolytic-uremic syndrome | HGNC:24338 | Homo sapiens (human) | 29071 | C1GALT1C1 |
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| DOID:0050731 | vitamin B12 deficiency | HGNC:4013 | Homo sapiens (human) | 2524 | FUT2 |
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| DOID:0080464 | developmental and epileptic encephalopathy 53 | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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| DOID:0060577 | 3MC syndrome 3 | HGNC:2220 | Homo sapiens (human) | 10584 | COLEC10 |
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| DOID:0080950 | alopecia-mental retardation syndrome 4 | HGNC:6708 | Homo sapiens (human) | 4047 | LSS |
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| DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | HGNC:15685 | Homo sapiens (human) | 11041 | B4GAT1 |
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| DOID:0111633 | congenital sucrase-isomaltase deficiency | HGNC:10856 | Homo sapiens (human) | 6476 | SI |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:1641 | Homo sapiens (human) | 30835 | CD209 |
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| DOID:612 | primary immunodeficiency disease | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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| DOID:0090064 | familial cold autoinflammatory syndrome 3 | HGNC:9066 | Homo sapiens (human) | 5336 | PLCG2 |
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| DOID:0070435 | hyperphosphatasia with impaired intellectual development syndrome 3 | HGNC:17893 | Homo sapiens (human) | 27315 | PGAP2 |
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| DOID:0080382 | nephrotic syndrome type 3 | HGNC:17175 | Homo sapiens (human) | 51196 | PLCE1 |
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