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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:104 | bacterial infectious disease | HGNC:11022 | Homo sapiens (human) | 7355 | SLC35A2 |
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| DOID:10763 | hypertension | HGNC:12524 | Homo sapiens (human) | 7357 | UGCG |
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| DOID:0112219 | developmental and epileptic encephalopathy 84 | HGNC:12525 | Homo sapiens (human) | 7358 | UGDH |
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| DOID:162 | cancer | HGNC:12527 | Homo sapiens (human) | 7360 | UGP2 |
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| DOID:0112218 | developmental and epileptic encephalopathy 83 | HGNC:12527 | Homo sapiens (human) | 7360 | UGP2 |
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| DOID:12712 | nephronophthisis | MGI:1920918 | Mus musculus (house mouse) | 73668 | Ttc21b |
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| DOID:2975 | cystic kidney disease | MGI:1920918 | Mus musculus (house mouse) | 73668 | Ttc21b |
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| DOID:0110088 | asphyxiating thoracic dystrophy 4 | MGI:1920918 | Mus musculus (house mouse) | 73668 | Ttc21b |
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| DOID:0111119 | nephronophthisis 12 | MGI:1920918 | Mus musculus (house mouse) | 73668 | Ttc21b |
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| DOID:0060062 | familial juvenile hyperuricemic nephropathy | HGNC:12559 | Homo sapiens (human) | 7369 | UMOD |
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| DOID:557 | kidney disease | HGNC:12559 | Homo sapiens (human) | 7369 | UMOD |
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| DOID:1793 | pancreatic cancer | HGNC:12562 | Homo sapiens (human) | 7371 | UCK2 |
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| DOID:13934 | facial paralysis | MGI:1920960 | Mus musculus (house mouse) | 73710 | Tubb2b |
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| DOID:0112227 | tubulinopathy | MGI:1920960 | Mus musculus (house mouse) | 73710 | Tubb2b |
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| DOID:0090132 | complex cortical dysplasia with other brain malformations 7 | MGI:1920960 | Mus musculus (house mouse) | 73710 | Tubb2b |
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| DOID:0050997 | cerebellar ataxia, mental retardation and dysequlibrium syndrome | MGI:1920960 | Mus musculus (house mouse) | 73710 | Tubb2b |
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| DOID:0060260 | ptosis | MGI:1920960 | Mus musculus (house mouse) | 73710 | Tubb2b |
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| DOID:0050833 | orotic aciduria | HGNC:12563 | Homo sapiens (human) | 7372 | UMPS |
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| DOID:653 | purine-pyrimidine metabolic disorder | HGNC:12563 | Homo sapiens (human) | 7372 | UMPS |
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| DOID:0111651 | ectodermal dysplasia 15 | MGI:1920970 | Mus musculus (house mouse) | 73720 | Cst6 |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | MGI:1920970 | Mus musculus (house mouse) | 73720 | Cst6 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:2191 | Homo sapiens (human) | 7373 | COL14A1 |
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| DOID:11702 | dysgammaglobulinemia | HGNC:12572 | Homo sapiens (human) | 7374 | UNG |
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| DOID:0060759 | immunodeficiency with hyper IgM type 5 | HGNC:12572 | Homo sapiens (human) | 7374 | UNG |
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| DOID:3525 | middle cerebral artery infarction | HGNC:12576 | Homo sapiens (human) | 7378 | UPP1 |
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