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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:2703 | synovitis | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:1070 | primary open angle glaucoma | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:2377 | multiple sclerosis | HGNC:20956 | Homo sapiens (human) | 9749 | PHACTR2 |
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| DOID:0070291 | primary autosomal recessive microcephaly 4 | HGNC:24054 | Homo sapiens (human) | 57082 | KNL1 |
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| DOID:11758 | iron deficiency anemia | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:11849 | Homo sapiens (human) | 7098 | TLR3 |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:6998 | Homo sapiens (human) | 4210 | MEFV |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:3007 | Homo sapiens (human) | 54344 | DPM3 |
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| DOID:0080554 | congenital disorder of glycosylation Ib | HGNC:7216 | Homo sapiens (human) | 4351 | MPI |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:10024 | migraine with aura | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:12365 | malaria | HGNC:1550 | Homo sapiens (human) | 875 | CBS |
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| DOID:0080188 | chronic myelomonocytic leukemia | HGNC:3527 | Homo sapiens (human) | 2146 | EZH2 |
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| DOID:8566 | herpes simplex | HGNC:6120 | Homo sapiens (human) | 3663 | IRF5 |
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| DOID:5419 | schizophrenia | HGNC:1102 | Homo sapiens (human) | 23774 | BRD1 |
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| DOID:0111896 | Diamond-Blackfan anemia 18 | HGNC:10310 | Homo sapiens (human) | 6141 | RPL18 |
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| DOID:4971 | myelofibrosis | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:10003 | sensorineural hearing loss | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:234 | colon adenocarcinoma | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:684 | hepatocellular carcinoma | HGNC:1733 | Homo sapiens (human) | 8621 | CDK13 |
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| DOID:9256 | colorectal cancer | HGNC:9646 | Homo sapiens (human) | 5783 | PTPN13 |
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| DOID:4029 | gastritis | HGNC:5331 | Homo sapiens (human) | 64127 | NOD2 |
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| DOID:0050548 | hereditary sensory neuropathy | HGNC:2976 | Homo sapiens (human) | 1786 | DNMT1 |
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| DOID:399 | tuberculosis | HGNC:2615 | Homo sapiens (human) | 1555 | CYP2B6 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:6182 | Homo sapiens (human) | 3710 | ITPR3 |
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