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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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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▼ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:219 | colon cancer | HGNC:882 | Homo sapiens (human) | 545 | ATR |
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| DOID:2861 | congenital nonspherocytic hemolytic anemia | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:9255 | frontotemporal dementia | HGNC:24537 | Homo sapiens (human) | 25978 | CHMP2B |
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| DOID:0060370 | Parkinson's disease 7 | HGNC:16369 | Homo sapiens (human) | 11315 | PARK7 |
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| DOID:1935 | Bardet-Biedl syndrome | HGNC:30000 | Homo sapiens (human) | 27241 | BBS9 |
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| DOID:3783 | Coffin-Lowry syndrome | HGNC:10432 | Homo sapiens (human) | 6197 | RPS6KA3 |
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| DOID:0110481 | autosomal recessive nonsyndromic deafness 23 | HGNC:14674 | Homo sapiens (human) | 65217 | PCDH15 |
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| DOID:0070444 | neurodevelopmental disorder with language delay and seizures | HGNC:11805 | Homo sapiens (human) | 7074 | TIAM1 |
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| DOID:0111114 | nephronophthisis 3 | HGNC:7907 | Homo sapiens (human) | 27031 | NPHP3 |
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| DOID:3535 | Unverricht-Lundborg syndrome | HGNC:2482 | Homo sapiens (human) | 1476 | CSTB |
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| DOID:2741 | bilirubin metabolic disorder | HGNC:10959 | Homo sapiens (human) | 10599 | SLCO1B1 |
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| DOID:0111960 | immunodeficiency 15A | HGNC:5960 | Homo sapiens (human) | 3551 | IKBKB |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:8743 | Homo sapiens (human) | 5122 | PCSK1 |
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| DOID:0060193 | amyotrophic lateral sclerosis type 1 | HGNC:11179 | Homo sapiens (human) | 6647 | SOD1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:320 | Homo sapiens (human) | 177 | AGER |
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| DOID:0080498 | ovarian dysgenesis 6 | HGNC:29914 | Homo sapiens (human) | 57122 | NUP107 |
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| DOID:5419 | schizophrenia | HGNC:1960 | Homo sapiens (human) | 1139 | CHRNA7 |
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| DOID:0110605 | primary ciliary dyskinesia 7 | HGNC:2942 | Homo sapiens (human) | 8701 | DNAH11 |
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| DOID:0080698 | Teebi hypertelorism syndrome 1 | HGNC:29022 | Homo sapiens (human) | 23384 | SPECC1L |
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| DOID:0090140 | cortisone reductase deficiency 2 | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:0110927 | nemaline myopathy 3 | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:10763 | hypertension | HGNC:244 | Homo sapiens (human) | 119 | ADD2 |
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| DOID:2908 | Treacher Collins syndrome | HGNC:11654 | Homo sapiens (human) | 6949 | TCOF1 |
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| DOID:0060350 | adenine phosphoribosyltransferase deficiency | HGNC:626 | Homo sapiens (human) | 353 | APRT |
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| DOID:0110910 | leukocyte adhesion deficiency 1 | HGNC:6155 | Homo sapiens (human) | 3689 | ITGB2 |
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