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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
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:10983 | Alport syndrome | HGNC:2204 | Homo sapiens (human) | 1285 | COL4A3 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:0110721 | neuronal ceroid lipofuscinosis 1 | HGNC:9325 | Homo sapiens (human) | 5538 | PPT1 |
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| DOID:13269 | hereditary coproporphyria | HGNC:2321 | Homo sapiens (human) | 1371 | CPOX |
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| DOID:12930 | dilated cardiomyopathy | HGNC:3049 | Homo sapiens (human) | 1829 | DSG2 |
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| DOID:0081419 | childhood-onset dystonia with optic atrophy and basal ganglia abnormalities | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
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| DOID:9970 | obesity | HGNC:7966 | Homo sapiens (human) | 10062 | NR1H3 |
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| DOID:10933 | obsessive-compulsive disorder | HGNC:1033 | Homo sapiens (human) | 627 | BDNF |
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| DOID:1324 | lung cancer | HGNC:9177 | Homo sapiens (human) | 5426 | POLE |
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| DOID:10325 | silicosis | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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| DOID:2843 | long QT syndrome | HGNC:6251 | Homo sapiens (human) | 3757 | KCNH2 |
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| DOID:12217 | Lewy body dementia | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:417 | Homo sapiens (human) | 229 | ALDOB |
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| DOID:0110671 | congenital myasthenic syndrome 6 | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:25941 | Homo sapiens (human) | 54790 | TET2 |
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| DOID:0080409 | familial adenomatous polyposis 1 | HGNC:583 | Homo sapiens (human) | 324 | APC |
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| DOID:0081265 | intellectual developmental disorder with abnormal behavior, microcephaly, and short stature | HGNC:26033 | Homo sapiens (human) | 54517 | PUS7 |
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| DOID:0060285 | parietal foramina | HGNC:450 | Homo sapiens (human) | 60529 | ALX4 |
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| DOID:12801 | mucopolysaccharidosis III | HGNC:10818 | Homo sapiens (human) | 6448 | SGSH |
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| DOID:0110159 | Charcot-Marie-Tooth disease type 2B | HGNC:9788 | Homo sapiens (human) | 7879 | RAB7A |
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| DOID:9884 | muscular dystrophy | HGNC:10807 | Homo sapiens (human) | 6444 | SGCD |
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| DOID:0050453 | lissencephaly | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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| DOID:0110913 | adult hypophosphatasia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:0111190 | distal myopathy 4 | HGNC:3756 | Homo sapiens (human) | 2318 | FLNC |
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| DOID:9970 | obesity | HGNC:6931 | Homo sapiens (human) | 4159 | MC3R |
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