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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:0080260 | autosomal recessive spinocerebellar ataxia 26 | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:0111537 | paroxysmal extreme pain disorder | HGNC:10597 | Homo sapiens (human) | 6335 | SCN9A |
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| DOID:0111495 | combined oxidative phosphorylation deficiency 33 | HGNC:1243 | Homo sapiens (human) | 708 | C1QBP |
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| 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:0112081 | nuclear type mitochondrial complex I deficiency 8 | HGNC:7710 | Homo sapiens (human) | 4722 | NDUFS3 |
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| DOID:2738 | pseudoxanthoma elasticum | HGNC:15516 | Homo sapiens (human) | 64131 | XYLT1 |
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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:0110809 | hereditary spastic paraplegia 57 | HGNC:11758 | Homo sapiens (human) | 10342 | TFG |
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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:0060780 | congenital diarrhea 6 | HGNC:4688 | Homo sapiens (human) | 2984 | GUCY2C |
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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:0112230 | lissencephaly 5 | HGNC:6486 | Homo sapiens (human) | 3912 | LAMB1 |
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| DOID:0111904 | autosomal recessive thrombophilia due to protein C deficiency | HGNC:9451 | Homo sapiens (human) | 5624 | PROC |
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| DOID:10534 | stomach cancer | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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| DOID:0060712 | autosomal recessive congenital ichthyosis 4A | HGNC:14637 | Homo sapiens (human) | 26154 | ABCA12 |
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| DOID:0060797 | hypomyelinating leukodystrophy 8 | HGNC:30348 | Homo sapiens (human) | 55703 | POLR3B |
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| DOID:0090091 | hypogonadotropic hypogonadism 23 with or without anosmia | HGNC:6584 | Homo sapiens (human) | 3972 | LHB |
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| DOID:0080416 | developmental and epileptic encephalopathy 32 | HGNC:6220 | Homo sapiens (human) | 3737 | KCNA2 |
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| DOID:0070471 | early-onset epilepsy 2 | HGNC:29010 | Homo sapiens (human) | 9739 | SETD1A |
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| DOID:0111907 | thrombophilia due to thrombin defect | HGNC:3531 | Homo sapiens (human) | 2162 | F13A1 |
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| DOID:0111669 | hyaline fibromatosis syndrome | HGNC:21732 | Homo sapiens (human) | 118429 | ANTXR2 |
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| DOID:0080264 | exudative vitreoretinopathy 7 | HGNC:2514 | Homo sapiens (human) | 1499 | CTNNB1 |
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