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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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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:0111913 | spermatogenic failure 30 | HGNC:20122 | Homo sapiens (human) | 122402 | TDRD9 |
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| DOID:0081188 | autosomal recessive intellectual developmental disorder 14 | HGNC:4551 | Homo sapiens (human) | 9524 | TECR |
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| DOID:0112363 | spondylocostal dysostosis 5 | HGNC:11605 | Homo sapiens (human) | 6911 | TBX6 |
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| DOID:0050650 | familial atrial fibrillation | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:0050773 | paraganglioma | HGNC:10981 | Homo sapiens (human) | 8402 | SLC25A11 |
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| DOID:0110734 | neurodegeneration with brain iron accumulation | HGNC:15578 | Homo sapiens (human) | 85021 | REPS1 |
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| DOID:0081074 | Teebi hypertelorism syndrome 2 | HGNC:1750 | Homo sapiens (human) | 1009 | CDH11 |
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| DOID:10123 | pigmentation disease | HGNC:6119 | Homo sapiens (human) | 3662 | IRF4 |
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| DOID:0070046 | Coffin-Siris syndrome 4 | HGNC:11100 | Homo sapiens (human) | 6597 | SMARCA4 |
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| DOID:0080758 | Fanconi renotubular syndrome 2 | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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| DOID:0111990 | immunodeficiency 30 | HGNC:5971 | Homo sapiens (human) | 3594 | IL12RB1 |
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| DOID:0080533 | Carney-Stratakis syndrome | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:0050454 | periventricular nodular heterotopia | HGNC:7728 | Homo sapiens (human) | 23327 | NEDD4L |
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| DOID:0110463 | autosomal recessive nonsyndromic deafness 102 | HGNC:3420 | Homo sapiens (human) | 2059 | EPS8 |
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| DOID:0081061 | nephrogenic diabetes insipidus type 2 | HGNC:634 | Homo sapiens (human) | 359 | AQP2 |
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| DOID:0080077 | hypophosphatemic nephrolithiasis/osteoporosis 1 | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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| DOID:0050777 | Joubert syndrome | HGNC:21424 | Homo sapiens (human) | 80173 | IFT74 |
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| DOID:0111863 | X-linked congenital bilateral absence of vas deferens | HGNC:4516 | Homo sapiens (human) | 10149 | ADGRG2 |
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| DOID:0060916 | proteasome-associated autoinflammatory syndrome 3 | HGNC:9541 | Homo sapiens (human) | 5692 | PSMB4 |
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| DOID:0080288 | spinocerebellar ataxia 46 | HGNC:17158 | Homo sapiens (human) | 23646 | PLD3 |
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| DOID:0111166 | molybdenum cofactor deficiency type C | HGNC:15465 | Homo sapiens (human) | 10243 | GPHN |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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| DOID:0080376 | trichorhinophalangeal syndrome type III | HGNC:12340 | Homo sapiens (human) | 7227 | TRPS1 |
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| DOID:0111071 | congenital bile acid synthesis defect 1 | HGNC:18324 | Homo sapiens (human) | 80270 | HSD3B7 |
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| DOID:0080567 | congenital disorder of glycosylation Ip | HGNC:32456 | Homo sapiens (human) | 440138 | ALG11 |
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