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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▼ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0050753 | cerebellar ataxia | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:0050573 | 2-hydroxyglutaric aciduria | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:0050574 | L-2-hydroxyglutaric aciduria | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:14330 | Parkinson's disease | HGNC:20407 | Homo sapiens (human) | 125972 | CALR3 |
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| DOID:0050441 | mucosulfatidosis | HGNC:20376 | Homo sapiens (human) | 285362 | SUMF1 |
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| DOID:0070459 | hereditary spastic paraplegia 90A | HGNC:20361 | Homo sapiens (human) | 171546 | SPTSSA |
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| DOID:0070460 | hereditary spastic paraplegia 90B | HGNC:20361 | Homo sapiens (human) | 171546 | SPTSSA |
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| DOID:0081122 | Catel Manzke syndrome | HGNC:20324 | Homo sapiens (human) | 23483 | TGDS |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:20266 | Homo sapiens (human) | 29880 | ALG5 |
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| DOID:0080322 | polycystic kidney disease | HGNC:20266 | Homo sapiens (human) | 29880 | ALG5 |
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| DOID:0080201 | Peters plus syndrome | HGNC:20207 | Homo sapiens (human) | 145173 | B3GLCT |
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| DOID:0081023 | retinal cone dystrophy 4 | HGNC:20202 | Homo sapiens (human) | 93589 | CACNA2D4 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:20197 | Homo sapiens (human) | 55343 | SLC35C1 |
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| DOID:0070255 | congenital disorder of glycosylation type IIc | HGNC:20197 | Homo sapiens (human) | 55343 | SLC35C1 |
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| DOID:0081312 | T-cell non-Hodgkin lymphoma | HGNC:20185 | Homo sapiens (human) | 54916 | TMEM260 |
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| DOID:10534 | stomach cancer | HGNC:20185 | Homo sapiens (human) | 54916 | TMEM260 |
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| DOID:0060060 | non-Hodgkin lymphoma | HGNC:20185 | Homo sapiens (human) | 54916 | TMEM260 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:20147 | Homo sapiens (human) | 51167 | CYB5R4 |
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| DOID:9970 | obesity | HGNC:20113 | Homo sapiens (human) | 123099 | DEGS2 |
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| DOID:1289 | neurodegenerative disease | HGNC:20113 | Homo sapiens (human) | 123099 | DEGS2 |
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| DOID:162 | cancer | HGNC:19980 | Homo sapiens (human) | 64841 | GNPNAT1 |
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| DOID:0080753 | keratosis follicularis spinulosa decalvans | HGNC:19980 | Homo sapiens (human) | 64841 | GNPNAT1 |
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| DOID:0060230 | basal ganglia calcification | HGNC:19918 | Homo sapiens (human) | 57462 | MYORG |
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| DOID:9256 | colorectal cancer | HGNC:19877 | Homo sapiens (human) | 79695 | GALNT12 |
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