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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:0081111 | osteosclerotic metaphyseal dysplasia | HGNC:18608 | Homo sapiens (human) | 79705 | LRRK1 |
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| DOID:0111946 | immunodeficiency 31C | HGNC:11362 | Homo sapiens (human) | 6772 | STAT1 |
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| DOID:0081267 | graft-versus-host disease | HGNC:3619 | Homo sapiens (human) | 2214 | FCGR3A |
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| DOID:12918 | thromboangiitis obliterans | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0112081 | nuclear type mitochondrial complex I deficiency 8 | HGNC:7710 | Homo sapiens (human) | 4722 | NDUFS3 |
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| DOID:13810 | familial hypercholesterolemia | HGNC:600 | Homo sapiens (human) | 335 | APOA1 |
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| DOID:3362 | coronary aneurysm | HGNC:7158 | Homo sapiens (human) | 4321 | MMP12 |
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| DOID:2738 | pseudoxanthoma elasticum | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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| DOID:11400 | pyelonephritis | HGNC:11847 | Homo sapiens (human) | 7096 | TLR1 |
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| DOID:8398 | osteoarthritis | HGNC:3959 | Homo sapiens (human) | 2487 | FRZB |
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| DOID:0111487 | combined oxidative phosphorylation deficiency 7 | HGNC:26784 | Homo sapiens (human) | 91574 | MTRFR |
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| DOID:3321 | GM2 gangliosidosis | HGNC:4367 | Homo sapiens (human) | 2760 | GM2A |
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| DOID:0110809 | hereditary spastic paraplegia 57 | HGNC:11758 | Homo sapiens (human) | 10342 | TFG |
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| DOID:674 | cleft palate | HGNC:9706 | Homo sapiens (human) | 5818 | NECTIN1 |
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| DOID:4947 | cholangiocarcinoma | HGNC:7059 | Homo sapiens (human) | 4255 | MGMT |
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| DOID:0080764 | hereditary diffuse gastric cancer | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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| DOID:0112149 | terminal osseous dysplasia | HGNC:3754 | Homo sapiens (human) | 2316 | FLNA |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:6844 | Homo sapiens (human) | 6416 | MAP2K4 |
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| DOID:13375 | temporal arteritis | HGNC:3619 | Homo sapiens (human) | 2214 | FCGR3A |
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| DOID:0060780 | congenital diarrhea 6 | HGNC:4688 | Homo sapiens (human) | 2984 | GUCY2C |
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| DOID:4483 | rhinitis | HGNC:6001 | Homo sapiens (human) | 3558 | IL2 |
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| DOID:8947 | diabetic retinopathy | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:3209 | junctional epidermolysis bullosa | HGNC:6493 | Homo sapiens (human) | 3918 | LAMC2 |
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| DOID:0111199 | autosomal dominant distal hereditary motor neuronopathy 7 | HGNC:14025 | Homo sapiens (human) | 60482 | SLC5A7 |
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| DOID:5603 | T-cell acute lymphoblastic leukemia | HGNC:8068 | Homo sapiens (human) | 4928 | NUP98 |
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