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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:0111465 | combined oxidative phosphorylation deficiency 21 | HGNC:30740 | Homo sapiens (human) | 80222 | TARS2 |
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| DOID:0080733 | Ehlers-Danlos syndrome dermatosparaxis type | HGNC:218 | Homo sapiens (human) | 9509 | ADAMTS2 |
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| DOID:0110595 | Stromme syndrome | HGNC:1857 | Homo sapiens (human) | 1063 | CENPF |
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| DOID:4166 | syphilis | HGNC:6340 | Homo sapiens (human) | 3813 | KIR3DS1 |
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| DOID:0111677 | familial benign fleck retina | HGNC:9038 | Homo sapiens (human) | 5322 | PLA2G5 |
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| DOID:0080626 | corticosterone methyloxidase deficiency 1 | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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| DOID:0112310 | central precocious puberty 1 | HGNC:4510 | Homo sapiens (human) | 84634 | KISS1R |
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| DOID:5295 | intestinal disease | HGNC:10906 | Homo sapiens (human) | 6555 | SLC10A2 |
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| DOID:1612 | breast cancer | HGNC:7794 | Homo sapiens (human) | 4790 | NFKB1 |
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| DOID:1168 | familial hyperlipidemia | HGNC:5233 | Homo sapiens (human) | 3304 | HSPA1B |
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| DOID:9074 | systemic lupus erythematosus | HGNC:5234 | Homo sapiens (human) | 3305 | HSPA1L |
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| DOID:11394 | adult respiratory distress syndrome | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:12205 | dengue disease | HGNC:1641 | Homo sapiens (human) | 30835 | CD209 |
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| DOID:0080411 | familial adenomatous polyposis 3 | HGNC:8028 | Homo sapiens (human) | 4913 | NTHL1 |
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| DOID:5409 | lung small cell carcinoma | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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| DOID:0110031 | hemoglobin H disease | HGNC:4824 | Homo sapiens (human) | 3040 | HBA2 |
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| DOID:1307 | dementia | HGNC:6700 | Homo sapiens (human) | 7804 | LRP8 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:320 | Homo sapiens (human) | 177 | AGER |
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| DOID:299 | adenocarcinoma | HGNC:583 | Homo sapiens (human) | 324 | APC |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:6000 | congestive heart failure | HGNC:11050 | Homo sapiens (human) | 6532 | SLC6A4 |
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| DOID:4797 | SM-AHNMD | HGNC:18318 | Homo sapiens (human) | 171023 | ASXL1 |
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| DOID:0080692 | Noonan syndrome-like disorder with loose anagen hair 1 | HGNC:15454 | Homo sapiens (human) | 8036 | SHOC2 |
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| DOID:3310 | atopic dermatitis | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:1612 | breast cancer | HGNC:2873 | Homo sapiens (human) | 1727 | CYB5R3 |
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