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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▲ |
|---|---|---|---|---|---|---|---|---|
| DOID:14723 | beta-ketothiolase deficiency | HGNC:93 | Homo sapiens (human) | 38 | ACAT1 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:18410 | Homo sapiens (human) | 23036 | ZNF292 |
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| DOID:0110501 | autosomal recessive nonsyndromic deafness 44 | HGNC:232 | Homo sapiens (human) | 107 | ADCY1 |
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| DOID:0060240 | UV-sensitive syndrome | HGNC:3438 | Homo sapiens (human) | 2074 | ERCC6 |
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| DOID:0111468 | combined oxidative phosphorylation deficiency 25 | HGNC:25133 | Homo sapiens (human) | 92935 | MARS2 |
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| DOID:0110757 | type 1 diabetes mellitus 20 | HGNC:11621 | Homo sapiens (human) | 6927 | HNF1A |
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| DOID:0111363 | Heinz body anemia | HGNC:4824 | Homo sapiens (human) | 3040 | HBA2 |
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| DOID:0060706 | X-linked lymphoproliferative syndrome 2 | HGNC:592 | Homo sapiens (human) | 331 | XIAP |
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| DOID:0110548 | autosomal dominant nonsyndromic deafness 17 | HGNC:7579 | Homo sapiens (human) | 4627 | MYH9 |
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| DOID:3526 | cerebral infarction | HGNC:3542 | Homo sapiens (human) | 2153 | F5 |
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| DOID:612 | primary immunodeficiency disease | HGNC:29271 | Homo sapiens (human) | 57169 | ZNFX1 |
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| DOID:0080732 | Ehlers-Danlos syndrome classic-like 2 | HGNC:303 | Homo sapiens (human) | 165 | AEBP1 |
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| DOID:12449 | aplastic anemia | HGNC:7652 | Homo sapiens (human) | 4683 | NBN |
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| DOID:0111729 | familial episodic pain syndrome 1 | HGNC:497 | Homo sapiens (human) | 8989 | TRPA1 |
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| DOID:0111344 | myeloproliferative disorder with eosinophilia | HGNC:8804 | Homo sapiens (human) | 5159 | PDGFRB |
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| DOID:0110394 | retinitis pigmentosa 44 | HGNC:9990 | Homo sapiens (human) | 5995 | RGR |
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| DOID:0070520 | peeling skin syndrome 1 | HGNC:1802 | Homo sapiens (human) | 1041 | CDSN |
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| DOID:0080664 | diaphyseal medullary stenosis with malignant fibrous histiocytoma | HGNC:7413 | Homo sapiens (human) | 4507 | MTAP |
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| DOID:0060299 | complement component 6 deficiency | HGNC:1339 | Homo sapiens (human) | 729 | C6 |
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| DOID:9253 | gastrointestinal stromal tumor | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:0111798 | X-linked nephrolithiasis type I | HGNC:2023 | Homo sapiens (human) | 1184 | CLCN5 |
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| DOID:0080242 | syndromic X-linked mental retardation Hough type | HGNC:19701 | Homo sapiens (human) | 22866 | CNKSR2 |
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| DOID:0060875 | isolated growth hormone deficiency type III | HGNC:1133 | Homo sapiens (human) | 695 | BTK |
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| DOID:0110285 | autosomal recessive limb-girdle muscular dystrophy type 2Q | HGNC:9069 | Homo sapiens (human) | 5339 | PLEC |
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| DOID:0080571 | congenital disorder of glycosylation Iu | HGNC:3006 | Homo sapiens (human) | 8818 | DPM2 |
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