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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:4362 | cervical cancer | HGNC:10771 | Homo sapiens (human) | 10262 | SF3B4 |
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| DOID:0110965 | brachydactyly type A2 | HGNC:1077 | Homo sapiens (human) | 658 | BMPR1B |
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| DOID:0081237 | acromesomelic dysplasia-3 | HGNC:1077 | Homo sapiens (human) | 658 | BMPR1B |
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| DOID:0050787 | juvenile polyposis syndrome | HGNC:1077 | Homo sapiens (human) | 658 | BMPR1B |
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| DOID:6432 | pulmonary hypertension | HGNC:1077 | Homo sapiens (human) | 658 | BMPR1B |
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| DOID:2256 | osteochondrodysplasia | HGNC:1077 | Homo sapiens (human) | 658 | BMPR1B |
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| DOID:2841 | asthma | HGNC:1077 | Homo sapiens (human) | 658 | BMPR1B |
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| DOID:0110978 | brachydactyly type A1D | HGNC:1077 | Homo sapiens (human) | 658 | BMPR1B |
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| DOID:2907 | Goldenhar syndrome | HGNC:10769 | Homo sapiens (human) | 10992 | SF3B2 |
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| DOID:9119 | acute myeloid leukemia | HGNC:10768 | Homo sapiens (human) | 23451 | SF3B1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:10768 | Homo sapiens (human) | 23451 | SF3B1 |
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| DOID:0050939 | uterine corpus endometrial carcinoma | HGNC:10768 | Homo sapiens (human) | 23451 | SF3B1 |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:10768 | Homo sapiens (human) | 23451 | SF3B1 |
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| DOID:4006 | bladder urothelial carcinoma | HGNC:10768 | Homo sapiens (human) | 23451 | SF3B1 |
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| DOID:1324 | lung cancer | HGNC:10761 | Homo sapiens (human) | 9869 | SETDB1 |
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| DOID:1909 | melanoma | HGNC:10761 | Homo sapiens (human) | 9869 | SETDB1 |
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| DOID:10283 | prostate cancer | HGNC:10761 | Homo sapiens (human) | 9869 | SETDB1 |
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| DOID:3070 | high grade glioma | HGNC:10761 | Homo sapiens (human) | 9869 | SETDB1 |
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| DOID:5419 | schizophrenia | HGNC:10761 | Homo sapiens (human) | 9869 | SETDB1 |
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| DOID:12849 | autistic disorder | HGNC:10761 | Homo sapiens (human) | 9869 | SETDB1 |
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| DOID:12858 | Huntington's disease | HGNC:10761 | Homo sapiens (human) | 9869 | SETDB1 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:10760 | Homo sapiens (human) | 6418 | SET |
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| DOID:384 | Wolff-Parkinson-White syndrome | HGNC:1076 | Homo sapiens (human) | 657 | BMPR1A |
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| DOID:0111686 | hereditary mixed polyposis syndrome 2 | HGNC:1076 | Homo sapiens (human) | 657 | BMPR1A |
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| DOID:5295 | intestinal disease | HGNC:1076 | Homo sapiens (human) | 657 | BMPR1A |
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