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GlyTouCan
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:3121 | gallbladder cancer | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:1227 | neutropenia | HGNC:11363 | Homo sapiens (human) | 6773 | STAT2 |
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| DOID:13544 | low tension glaucoma | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0050636 | familial visceral amyloidosis | HGNC:3661 | Homo sapiens (human) | 2243 | FGA |
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| DOID:1184 | nephrotic syndrome | RGD:3639 | Rattus norvegicus (Norway rat) | 25122 | Scnn1a |
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| DOID:0070267 | congenital disorder of glycosylation type IIo | HGNC:28178 | Homo sapiens (human) | 84317 | CCDC115 |
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| DOID:0112350 | spermatogenic failure 61 | HGNC:11356 | Homo sapiens (human) | 10734 | STAG3 |
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| DOID:11394 | adult respiratory distress syndrome | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:0110386 | retinitis pigmentosa 42 | HGNC:15646 | Homo sapiens (human) | 55975 | KLHL7 |
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| DOID:1554 | vibratory urticaria | HGNC:3337 | Homo sapiens (human) | 30817 | ADGRE2 |
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| DOID:0070209 | hereditary lymphedema ID | HGNC:12682 | Homo sapiens (human) | 7424 | VEGFC |
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| DOID:9410 | panhypopituitarism | HGNC:18666 | Homo sapiens (human) | 55599 | RNPC3 |
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| DOID:10763 | hypertension | HGNC:3023 | Homo sapiens (human) | 1813 | DRD2 |
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| DOID:12361 | Graves' disease | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:0080058 | autosomal recessive spinocerebellar ataxia 14 | HGNC:11276 | Homo sapiens (human) | 6712 | SPTBN2 |
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| DOID:1024 | leprosy | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:589 | congenital hemolytic anemia | HGNC:4827 | Homo sapiens (human) | 3043 | HBB |
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| DOID:0080082 | nonsyndromic congenital nail disorder 4 | HGNC:16175 | Homo sapiens (human) | 343637 | RSPO4 |
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| DOID:9296 | cleft lip | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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| DOID:0080473 | developmental delay and seizures with or without movement abnormalities | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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| DOID:0080322 | polycystic kidney disease | HGNC:4138 | Homo sapiens (human) | 23193 | GANAB |
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| DOID:10003 | sensorineural hearing loss | HGNC:7579 | Homo sapiens (human) | 4627 | MYH9 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:9722 | Homo sapiens (human) | 5832 | ALDH18A1 |
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| DOID:8692 | myeloid leukemia | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:13375 | temporal arteritis | HGNC:6014 | Homo sapiens (human) | 3565 | IL4 |
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