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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:1094 | attention deficit hyperactivity disorder | HGNC:5006 | Homo sapiens (human) | 3156 | HMGCR |
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| DOID:0080441 | developmental and epileptic encephalopathy 49 | HGNC:19344 | Homo sapiens (human) | 23258 | DENND5A |
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| DOID:10283 | prostate cancer | HGNC:6358 | Homo sapiens (human) | 5655 | KLK10 |
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| DOID:1993 | rectum cancer | HGNC:6876 | Homo sapiens (human) | 1432 | MAPK14 |
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| DOID:0050856 | oppositional defiant disorder | HGNC:644 | Homo sapiens (human) | 367 | AR |
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| DOID:419 | scleroderma | HGNC:4931 | Homo sapiens (human) | 3105 | HLA-A |
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| DOID:648 | kuru | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:11266 | Hantavirus hemorrhagic fever with renal syndrome | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:10003 | sensorineural hearing loss | HGNC:16035 | Homo sapiens (human) | 161497 | STRC |
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| DOID:1206 | Rett syndrome | HGNC:11411 | Homo sapiens (human) | 6792 | CDKL5 |
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| DOID:0060058 | lymphoma | HGNC:6819 | Homo sapiens (human) | 10892 | MALT1 |
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| DOID:3146 | lipid metabolism disorder | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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| DOID:12849 | autistic disorder | HGNC:4076 | Homo sapiens (human) | 2555 | GABRA2 |
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| DOID:0111308 | familial febrile seizures 11 | HGNC:17245 | Homo sapiens (human) | 57094 | CPA6 |
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| DOID:0050777 | Joubert syndrome | HGNC:694 | Homo sapiens (human) | 403 | ARL3 |
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| DOID:13533 | osteopetrosis | HGNC:11028 | Homo sapiens (human) | 6522 | SLC4A2 |
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| DOID:11054 | urinary bladder cancer | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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| DOID:3234 | central nervous system lymphoma | HGNC:7562 | Homo sapiens (human) | 4615 | MYD88 |
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| DOID:8947 | diabetic retinopathy | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:0070271 | Lynch syndrome 1 | HGNC:7325 | Homo sapiens (human) | 4436 | MSH2 |
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| DOID:0111678 | hereditary folate malabsorption | HGNC:30521 | Homo sapiens (human) | 113235 | SLC46A1 |
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| DOID:13809 | familial combined hyperlipidemia | HGNC:610 | Homo sapiens (human) | 345 | APOC3 |
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| DOID:14067 | Plasmodium falciparum malaria | HGNC:5141 | Homo sapiens (human) | 3240 | HP |
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| DOID:0050591 | tooth agenesis | HGNC:6698 | Homo sapiens (human) | 4040 | LRP6 |
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| DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | HGNC:15685 | Homo sapiens (human) | 11041 | B4GAT1 |
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