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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:3209 | junctional epidermolysis bullosa | HGNC:6139 | Homo sapiens (human) | 3675 | ITGA3 |
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| DOID:12720 | cerebral atherosclerosis | HGNC:4814 | Homo sapiens (human) | 8997 | KALRN |
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| DOID:0050637 | Finnish type amyloidosis | HGNC:4620 | Homo sapiens (human) | 2934 | GSN |
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| DOID:1380 | endometrial cancer | HGNC:18505 | Homo sapiens (human) | 54894 | RNF43 |
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| DOID:0112376 | muscular dystrophy-dystroglycanopathy type B15 | HGNC:3007 | Homo sapiens (human) | 54344 | DPM3 |
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| DOID:0060241 | 3-M syndrome | HGNC:21024 | Homo sapiens (human) | 9820 | CUL7 |
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| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | HGNC:21304 | Homo sapiens (human) | 54936 | ADPRS |
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| DOID:0080585 | Van Maldergem syndrome 1 | HGNC:13681 | Homo sapiens (human) | 8642 | DCHS1 |
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| DOID:3526 | cerebral infarction | HGNC:7468 | Homo sapiens (human) | 4548 | MTR |
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| DOID:0070072 | autosomal dominant intellectual developmental disorder 42 | HGNC:4396 | Homo sapiens (human) | 2782 | GNB1 |
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| DOID:3526 | cerebral infarction | HGNC:9205 | Homo sapiens (human) | 5445 | PON2 |
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| DOID:2671 | transitional cell carcinoma | HGNC:583 | Homo sapiens (human) | 324 | APC |
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| DOID:5409 | lung small cell carcinoma | HGNC:6490 | Homo sapiens (human) | 3914 | LAMB3 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:4187 | Homo sapiens (human) | 2638 | GC |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:589 | congenital hemolytic anemia | HGNC:11027 | Homo sapiens (human) | 6521 | SLC4A1 |
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| DOID:0081152 | common variable immunodeficiency 10 | HGNC:7795 | Homo sapiens (human) | 4791 | NFKB2 |
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| DOID:2799 | bronchiolitis obliterans | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:3312 | bipolar disorder | HGNC:4079 | Homo sapiens (human) | 2558 | GABRA5 |
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| DOID:2043 | hepatitis B | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:3691 | Homo sapiens (human) | 2264 | FGFR4 |
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| DOID:9410 | panhypopituitarism | HGNC:10249 | Homo sapiens (human) | 6091 | ROBO1 |
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| DOID:0060470 | salt and pepper syndrome | HGNC:10872 | Homo sapiens (human) | 8869 | ST3GAL5 |
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| DOID:8893 | psoriasis | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:1324 | lung cancer | HGNC:7155 | Homo sapiens (human) | 4312 | MMP1 |
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