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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
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:1790 | malignant mesothelioma | HGNC:18420 | Homo sapiens (human) | 29072 | SETD2 |
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| DOID:1324 | lung cancer | HGNC:3430 | Homo sapiens (human) | 2064 | ERBB2 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:18170 | Homo sapiens (human) | 51727 | CMPK1 |
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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:1924 | hypogonadism | HGNC:4510 | Homo sapiens (human) | 84634 | KISS1R |
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| DOID:10534 | stomach cancer | HGNC:7527 | Homo sapiens (human) | 4595 | MUTYH |
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| DOID:12361 | Graves' disease | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:5844 | myocardial infarction | HGNC:6692 | Homo sapiens (human) | 4035 | LRP1 |
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| DOID:3883 | Lynch syndrome | HGNC:11773 | Homo sapiens (human) | 7048 | TGFBR2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0081101 | nonautoimmune hyperthyroidism | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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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:3907 | lung squamous cell carcinoma | HGNC:11730 | Homo sapiens (human) | 7015 | TERT |
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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:0111732 | Eiken syndrome | HGNC:9608 | Homo sapiens (human) | 5745 | PTH1R |
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| DOID:0050475 | Weill-Marchesani syndrome | HGNC:6715 | Homo sapiens (human) | 4053 | LTBP2 |
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| DOID:848 | arthritis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:769 | neuroblastoma | HGNC:14234 | Homo sapiens (human) | 64324 | NSD1 |
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| DOID:2560 | morphine dependence | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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