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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:850 | lung disease | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:12509 | Homo sapiens (human) | 29978 | UBQLN2 |
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| DOID:0110768 | hereditary spastic paraplegia 15 | HGNC:20761 | Homo sapiens (human) | 23503 | ZFYVE26 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9235 | Homo sapiens (human) | 5467 | PPARD |
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| DOID:5419 | schizophrenia | HGNC:17091 | Homo sapiens (human) | 23385 | NCSTN |
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| DOID:10763 | hypertension | HGNC:2642 | Homo sapiens (human) | 1579 | CYP4A11 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
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| DOID:14705 | Pfeiffer syndrome | HGNC:3689 | Homo sapiens (human) | 2263 | FGFR2 |
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| DOID:0090142 | cystathioninuria | HGNC:2501 | Homo sapiens (human) | 1491 | CTH |
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| DOID:12930 | dilated cardiomyopathy | HGNC:7577 | Homo sapiens (human) | 4625 | MYH7 |
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| DOID:0110197 | Charcot-Marie-Tooth disease dominant intermediate B | HGNC:2974 | Homo sapiens (human) | 1785 | DNM2 |
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| DOID:856 | biotinidase deficiency | HGNC:1122 | Homo sapiens (human) | 686 | BTD |
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| DOID:0080062 | autosomal recessive spinocerebellar ataxia 13 | HGNC:4593 | Homo sapiens (human) | 2911 | GRM1 |
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| DOID:0060589 | Yunis-Varon syndrome | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0081112 | Baraitser-Winter syndrome 1 | HGNC:132 | Homo sapiens (human) | 60 | ACTB |
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| DOID:14330 | Parkinson's disease | HGNC:7458 | Homo sapiens (human) | 4537 | ND3 |
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| DOID:0112135 | severe congenital neutropenia 8 | HGNC:11301 | Homo sapiens (human) | 6729 | SRP54 |
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| DOID:0090004 | progressive pseudorheumatoid arthropathy of childhood | HGNC:12771 | Homo sapiens (human) | 8838 | CCN6 |
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| DOID:0050700 | cardiomyopathy | HGNC:7577 | Homo sapiens (human) | 4625 | MYH7 |
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| DOID:0111393 | mucopolysaccharidosis type IIIC | HGNC:26527 | Homo sapiens (human) | 138050 | HGSNAT |
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| DOID:12801 | mucopolysaccharidosis III | HGNC:4422 | Homo sapiens (human) | 2799 | GNS |
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| DOID:0110191 | Charcot-Marie-Tooth disease type 4B1 | HGNC:7450 | Homo sapiens (human) | 8898 | MTMR2 |
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| DOID:10763 | hypertension | HGNC:9958 | Homo sapiens (human) | 5972 | REN |
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| DOID:0080235 | autosomal dominant intellectual developmental disorder 48 | HGNC:9801 | Homo sapiens (human) | 5879 | RAC1 |
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| DOID:0080042 | autosomal recessive spinocerebellar ataxia 18 | HGNC:4576 | Homo sapiens (human) | 2895 | GRID2 |
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