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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:0090103 | Huntington's disease-like 1 | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:0112202 | developmental and epileptic encephalopathy | HGNC:18423 | Homo sapiens (human) | 9681 | DEPDC5 |
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| DOID:0110167 | Charcot-Marie-Tooth disease axonal type 2K | HGNC:14201 | Homo sapiens (human) | 56704 | JPH1 |
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| DOID:0111801 | syndromic microphthalmia 3 | HGNC:11195 | Homo sapiens (human) | 6657 | SOX2 |
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| DOID:8986 | narcolepsy | HGNC:7197 | Homo sapiens (human) | 4340 | MOG |
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| DOID:0112180 | urocanase deficiency | HGNC:26444 | Homo sapiens (human) | 131669 | UROC1 |
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| DOID:0050791 | persistent Mullerian duct syndrome | HGNC:464 | Homo sapiens (human) | 268 | AMH |
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| DOID:14735 | hereditary angioedema | HGNC:6383 | Homo sapiens (human) | 3827 | KNG1 |
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| DOID:0111210 | autosomal dominant distal hereditary motor neuronopathy 6 | HGNC:28844 | Homo sapiens (human) | 81545 | FBXO38 |
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| DOID:0111715 | Schaaf-Yang syndrome | HGNC:6814 | Homo sapiens (human) | 54551 | MAGEL2 |
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| DOID:0081223 | glycosylphosphatidylinositol biosynthesis defect 16 | HGNC:8960 | Homo sapiens (human) | 5279 | PIGC |
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| DOID:0110647 | long QT syndrome 5 | HGNC:6240 | Homo sapiens (human) | 3753 | KCNE1 |
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| DOID:0070454 | hereditary spastic paraplegia 70 | HGNC:6898 | Homo sapiens (human) | 4141 | MARS1 |
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| DOID:0060304 | dyschromatosis universalis hereditaria | HGNC:47 | Homo sapiens (human) | 10058 | ABCB6 |
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| DOID:0112182 | mismatch repair cancer syndrome | HGNC:7325 | Homo sapiens (human) | 4436 | MSH2 |
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| DOID:8454 | riboflavin deficiency | HGNC:30225 | Homo sapiens (human) | 55065 | SLC52A1 |
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| DOID:0070403 | hypomyelinating leukodystrophy 26 | HGNC:16872 | Homo sapiens (human) | 347734 | SLC35B2 |
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| DOID:4253 | melorheostosis | HGNC:6840 | Homo sapiens (human) | 5604 | MAP2K1 |
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| DOID:0080681 | X-linked chronic idiopathic intestinal pseudo-obstruction | HGNC:3754 | Homo sapiens (human) | 2316 | FLNA |
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| DOID:0070049 | autosomal dominant intellectual developmental disorder 19 | HGNC:2514 | Homo sapiens (human) | 1499 | CTNNB1 |
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| DOID:612 | primary immunodeficiency disease | HGNC:18043 | Homo sapiens (human) | 55388 | MCM10 |
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| DOID:1588 | thrombocytopenia | HGNC:4036 | Homo sapiens (human) | 2533 | FYB1 |
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| DOID:0081443 | Stolerman neurodevelopmental syndrome | HGNC:29012 | Homo sapiens (human) | 23135 | KDM6B |
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| DOID:0081046 | frontonasal dysplasia 2 | HGNC:450 | Homo sapiens (human) | 60529 | ALX4 |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:21350 | Homo sapiens (human) | 8050 | PDHX |
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