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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
LM-GlycoRepo
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:11830 | myopia | HGNC:8547 | Homo sapiens (human) | 8974 | P4HA2 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:16787 | Homo sapiens (human) | 80267 | EDEM3 |
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| DOID:0080839 | X-linked warfarin sensitivity | HGNC:3551 | Homo sapiens (human) | 2158 | F9 |
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| DOID:0111086 | Fanconi anemia complementation group G | HGNC:3588 | Homo sapiens (human) | 2189 | FANCG |
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| DOID:12678 | hypercalcemia | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:19263 | Homo sapiens (human) | 81562 | LMAN2L |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:19987 | Homo sapiens (human) | 284656 | EPHA10 |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:0081297 | oculopharyngodistal myopathy 1 | HGNC:31708 | Homo sapiens (human) | 29967 | LRP12 |
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| DOID:936 | brain disease | HGNC:24858 | Homo sapiens (human) | 56947 | MFF |
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| DOID:0111681 | glutamate-cysteine ligase deficiency | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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| DOID:0080289 | orofaciodigital syndrome XVII | HGNC:29239 | Homo sapiens (human) | 27152 | INTU |
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| DOID:0060060 | non-Hodgkin lymphoma | HGNC:9360 | Homo sapiens (human) | 5551 | PRF1 |
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| DOID:0111866 | trichothiodystrophy | HGNC:6898 | Homo sapiens (human) | 4141 | MARS1 |
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| DOID:0111644 | autosomal recessive nonsyndromic deafness 110 | HGNC:2180 | Homo sapiens (human) | 1690 | COCH |
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| DOID:0081202 | autosomal recessive intellectual developmental disorder 37 | HGNC:494 | Homo sapiens (human) | 288 | ANK3 |
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| DOID:612 | primary immunodeficiency disease | HGNC:9666 | Homo sapiens (human) | 5788 | PTPRC |
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| DOID:0081190 | autosomal recessive intellectual developmental disorder 18 | HGNC:2372 | Homo sapiens (human) | 9439 | MED23 |
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| DOID:9256 | colorectal cancer | HGNC:2701 | Homo sapiens (human) | 1630 | DCC |
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| DOID:0111797 | autosomal recessive congenital nystagmus | HGNC:10249 | Homo sapiens (human) | 6091 | ROBO1 |
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| DOID:0111651 | ectodermal dysplasia 15 | HGNC:2478 | Homo sapiens (human) | 1474 | CST6 |
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| DOID:0080386 | nephrotic syndrome type 10 | HGNC:3334 | Homo sapiens (human) | 2013 | EMP2 |
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| DOID:0111581 | C syndrome | HGNC:16892 | Homo sapiens (human) | 10225 | CD96 |
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| DOID:0080109 | infantile myofibromatosis | HGNC:7883 | Homo sapiens (human) | 4854 | NOTCH3 |
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| DOID:0111698 | proprotein convertase 1/3 deficiency | HGNC:8743 | Homo sapiens (human) | 5122 | PCSK1 |
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