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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:13641 | exfoliation syndrome | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:14681 | Silver-Russell syndrome | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:9976 | heroin dependence | HGNC:2615 | Homo sapiens (human) | 1555 | CYP2B6 |
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| DOID:0080533 | Carney-Stratakis syndrome | HGNC:10682 | Homo sapiens (human) | 6391 | SDHC |
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| DOID:0060496 | respiratory allergy | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0111156 | spermatogenic failure 9 | HGNC:19414 | Homo sapiens (human) | 283417 | DPY19L2 |
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| DOID:0112022 | non-syndromic X-linked intellectual disability 21 | HGNC:5996 | Homo sapiens (human) | 11141 | IL1RAPL1 |
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| DOID:583 | hemolytic anemia | HGNC:8896 | Homo sapiens (human) | 5230 | PGK1 |
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| DOID:2043 | hepatitis B | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:14938 | Homo sapiens (human) | 51604 | PIGT |
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| DOID:4928 | intrahepatic cholangiocarcinoma | HGNC:5382 | Homo sapiens (human) | 3417 | IDH1 |
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| DOID:0110818 | hereditary spastic paraplegia 73 | HGNC:18540 | Homo sapiens (human) | 126129 | CPT1C |
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| DOID:0111392 | mucopolysaccharidosis type IVB | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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| DOID:9256 | colorectal cancer | HGNC:14897 | Homo sapiens (human) | 80271 | ITPKC |
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| DOID:0111068 | congenital bile acid synthesis defect 4 | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:3211 | lysosomal storage disease | HGNC:9251 | Homo sapiens (human) | 5476 | CTSA |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:9993 | hypoglycemia | HGNC:2623 | Homo sapiens (human) | 1559 | CYP2C9 |
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| DOID:0060256 | Dowling-Degos disease | HGNC:14988 | Homo sapiens (human) | 23509 | POFUT1 |
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| DOID:14080 | glucocorticoid-remediable aldosteronism | HGNC:2591 | Homo sapiens (human) | 1584 | CYP11B1 |
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| DOID:4971 | myelofibrosis | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:0060645 | chronic recurrent multifocal osteomyelitis | HGNC:5993 | Homo sapiens (human) | 3554 | IL1R1 |
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| DOID:0112300 | spondylometaphyseal dysplasia with cone-rod dystrophy | HGNC:8754 | Homo sapiens (human) | 5130 | PCYT1A |
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