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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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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:0050558 | Ullrich congenital muscular dystrophy | MGI:88461 | Mus musculus (house mouse) | 12835 | Col6a3 |
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| DOID:5082 | liver cirrhosis | HGNC:4606 | Homo sapiens (human) | 2923 | PDIA3 |
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| DOID:9870 | galactosemia | MGI:95638 | Mus musculus (house mouse) | 14430 | Galt |
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| DOID:1574 | alcohol use disorder | HGNC:8153 | Homo sapiens (human) | 4985 | OPRD1 |
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| DOID:10763 | hypertension | HGNC:6293 | Homo sapiens (human) | 3783 | KCNN4 |
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| DOID:0110640 | congenital muscular dystrophy due to LMNA mutation | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:10618 | Homo sapiens (human) | 6347 | CCL2 |
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| DOID:0110722 | neuronal ceroid lipofuscinosis 7 | MGI:1919425 | Mus musculus (house mouse) | 72175 | Mfsd8 |
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| DOID:684 | hepatocellular carcinoma | HGNC:6950 | Homo sapiens (human) | 4176 | MCM7 |
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| DOID:0111181 | familial hemiplegic migraine 1 | FB:FBgn0263111 | Drosophila melanogaster (fruit fly) | 32158 | cac |
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| DOID:224 | transient cerebral ischemia | HGNC:4432 | Homo sapiens (human) | 2805 | GOT1 |
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| DOID:10762 | portal hypertension | HGNC:19964 | Homo sapiens (human) | 22846 | VASH1 |
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| DOID:0070290 | primary autosomal recessive microcephaly 6 | FB:FBgn0011020 | Drosophila melanogaster (fruit fly) | 40859 | Sas-4 |
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| DOID:6432 | pulmonary hypertension | HGNC:11730 | Homo sapiens (human) | 7015 | TERT |
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| DOID:11394 | adult respiratory distress syndrome | HGNC:16 | Homo sapiens (human) | 12 | SERPINA3 |
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| DOID:9976 | heroin dependence | RGD:69426 | Rattus norvegicus (Norway rat) | 29335 | Oprk1 |
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| DOID:850 | lung disease | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:0110030 | alpha thalassemia-X-linked intellectual disability syndrome | HGNC:886 | Homo sapiens (human) | 546 | ATRX |
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| DOID:0080124 | mitochondrial DNA depletion syndrome 5 | MGI:1306775 | Mus musculus (house mouse) | 20916 | Sucla2 |
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| DOID:9119 | acute myeloid leukemia | MGI:95559 | Mus musculus (house mouse) | 14255 | Flt3 |
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| DOID:0060559 | lethal congenital contracture syndrome 1 | SGD:S000002366 | Saccharomyces cerevisiae S288C | 851320 | GLE1 |
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| DOID:0060756 | sclerosteosis 1 | MGI:1921749 | Mus musculus (house mouse) | 74499 | Sost |
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| DOID:0050908 | myelodysplastic syndrome | MGI:2684063 | Mus musculus (house mouse) | 228790 | Asxl1 |
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| DOID:8670 | eating disorder | HGNC:14063 | Homo sapiens (human) | 9759 | HDAC4 |
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