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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:0050834 | CHARGE syndrome | FB:FBgn0266557 | Drosophila melanogaster (fruit fly) | 33185 | kis |
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| DOID:3310 | atopic dermatitis | MGI:96541 | Mus musculus (house mouse) | 16163 | Il13 |
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| DOID:0050776 | non-syndromic X-linked intellectual disability | MGI:99846 | Mus musculus (house mouse) | 14567 | Gdi1 |
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| DOID:8947 | diabetic retinopathy | HGNC:3176 | Homo sapiens (human) | 1906 | EDN1 |
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| DOID:2841 | asthma | RGD:3667 | Rattus norvegicus (Norway rat) | 25350 | Sftpd |
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| DOID:1596 | depressive disorder | RGD:3729 | Rattus norvegicus (Norway rat) | 29219 | Snca |
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| DOID:11119 | Gilles de la Tourette syndrome | MGI:2679446 | Mus musculus (house mouse) | 76965 | Slitrk1 |
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| DOID:9970 | obesity | RGD:2886 | Rattus norvegicus (Norway rat) | 25325 | Il10 |
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| DOID:1852 | intrahepatic cholestasis | HGNC:45 | Homo sapiens (human) | 5244 | ABCB4 |
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| DOID:10652 | Alzheimer's disease | HGNC:8032 | Homo sapiens (human) | 4915 | NTRK2 |
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| DOID:8997 | polycythemia vera | HGNC:3309 | Homo sapiens (human) | 1991 | ELANE |
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| DOID:12858 | Huntington's disease | HGNC:3113 | Homo sapiens (human) | 1869 | E2F1 |
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| DOID:5408 | Paget's disease of bone | MGI:107931 | Mus musculus (house mouse) | 18412 | Sqstm1 |
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| DOID:10588 | adrenoleukodystrophy | SGD:S000001671 | Saccharomyces cerevisiae S288C | 853647 | PXA2 |
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| DOID:10588 | adrenoleukodystrophy | SGD:S000006068 | Saccharomyces cerevisiae S288C | 855956 | PXA1 |
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| DOID:12347 | osteogenesis imperfecta | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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| DOID:1686 | glaucoma | HGNC:11141 | Homo sapiens (human) | 6623 | SNCG |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:8824 | Homo sapiens (human) | 5176 | SERPINF1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:14330 | Parkinson's disease | HGNC:5241 | Homo sapiens (human) | 3312 | HSPA8 |
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| DOID:0110593 | autosomal dominant nonsyndromic deafness 9 | MGI:1278313 | Mus musculus (house mouse) | 12810 | Coch |
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| DOID:10159 | osteonecrosis | HGNC:11760 | Homo sapiens (human) | 7035 | TFPI |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11289 | Homo sapiens (human) | 6720 | SREBF1 |
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| DOID:9970 | obesity | HGNC:9236 | Homo sapiens (human) | 5468 | PPARG |
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| DOID:12930 | dilated cardiomyopathy | HGNC:3049 | Homo sapiens (human) | 1829 | DSG2 |
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