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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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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:0112205 | developmental and epileptic encephalopathy 69 | HGNC:1392 | Homo sapiens (human) | 777 | CACNA1E |
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| DOID:0111548 | ring dermoid of cornea | HGNC:9005 | Homo sapiens (human) | 5308 | PITX2 |
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| DOID:0112004 | immunodeficiency 71 | HGNC:704 | Homo sapiens (human) | 10095 | ARPC1B |
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| DOID:1324 | lung cancer | HGNC:3430 | Homo sapiens (human) | 2064 | ERBB2 |
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| DOID:0070296 | primary autosomal recessive microcephaly | HGNC:28952 | Homo sapiens (human) | 23310 | NCAPD3 |
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| DOID:0111672 | primary hyperoxaluria type 3 | HGNC:25155 | Homo sapiens (human) | 112817 | HOGA1 |
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| DOID:0110317 | hypertrophic cardiomyopathy 11 | HGNC:143 | Homo sapiens (human) | 70 | ACTC1 |
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| DOID:10534 | stomach cancer | HGNC:7527 | Homo sapiens (human) | 4595 | MUTYH |
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| DOID:10825 | essential hypertension | HGNC:2638 | Homo sapiens (human) | 1577 | CYP3A5 |
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| DOID:0110272 | cataract 40 | HGNC:7820 | Homo sapiens (human) | 4810 | NHS |
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| DOID:0081102 | familial gestational hyperthyroidism | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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| DOID:6846 | familial melanoma | HGNC:11730 | Homo sapiens (human) | 7015 | TERT |
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| DOID:0060639 | permanent neonatal diabetes mellitus | HGNC:59 | Homo sapiens (human) | 6833 | ABCC8 |
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| DOID:0080759 | Fanconi renotubular syndrome 3 | HGNC:3247 | Homo sapiens (human) | 1962 | EHHADH |
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| DOID:0070063 | autosomal dominant intellectual developmental disorder 33 | HGNC:3010 | Homo sapiens (human) | 1804 | DPP6 |
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| DOID:2218 | blood platelet disease | HGNC:6156 | Homo sapiens (human) | 3690 | ITGB3 |
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| DOID:0110651 | long QT syndrome 10 | HGNC:10592 | Homo sapiens (human) | 6330 | SCN4B |
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| DOID:5723 | optic atrophy | HGNC:11317 | Homo sapiens (human) | 6742 | SSBP1 |
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| DOID:0111551 | neurogenic scapuloperoneal syndrome Kaeser type | HGNC:2770 | Homo sapiens (human) | 1674 | DES |
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| DOID:0111909 | autosomal dominant thrombophilia due to protein C deficiency | HGNC:9451 | Homo sapiens (human) | 5624 | PROC |
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| DOID:0070205 | familial partial lipodystrophy type 4 | HGNC:9076 | Homo sapiens (human) | 5346 | PLIN1 |
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| DOID:0111371 | isolated hyperchlorhidrosis | HGNC:1371 | Homo sapiens (human) | 771 | CA12 |
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| DOID:13777 | epidermodysplasia verruciformis | HGNC:6023 | Homo sapiens (human) | 3574 | IL7 |
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| DOID:0050580 | hereditary lymphedema | HGNC:1850 | Homo sapiens (human) | 9620 | CELSR1 |
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| DOID:0111538 | paramyotonia congenita of Von Eulenburg | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
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