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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
LM-GlycoRepo
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:0050456 | Buruli ulcer disease | HGNC:10907 | Homo sapiens (human) | 6556 | SLC11A1 |
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| DOID:12365 | malaria | HGNC:4702 | Homo sapiens (human) | 2993 | GYPA |
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| DOID:0110367 | retinitis pigmentosa 38 | HGNC:7027 | Homo sapiens (human) | 10461 | MERTK |
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| DOID:0081442 | blepharophimosis-impaired intellectual development syndrome | HGNC:11098 | Homo sapiens (human) | 6595 | SMARCA2 |
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| DOID:9277 | primary cerebellar degeneration | HGNC:24624 | Homo sapiens (human) | 64374 | SIL1 |
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| DOID:0112318 | Schindler disease type 1 | HGNC:7631 | Homo sapiens (human) | 4668 | NAGA |
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| DOID:0111017 | cone-rod dystrophy 10 | HGNC:10729 | Homo sapiens (human) | 64218 | SEMA4A |
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| DOID:0050647 | Arts syndrome | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:0080785 | Brown-Vialetto-Van Laere syndrome 1 | HGNC:16187 | Homo sapiens (human) | 113278 | SLC52A3 |
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| DOID:0112368 | Coffin-Siris syndrome 5 | HGNC:11109 | Homo sapiens (human) | 6605 | SMARCE1 |
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| DOID:0090131 | complex cortical dysplasia with other brain malformations | HGNC:19946 | Homo sapiens (human) | 157922 | CAMSAP1 |
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| DOID:0050591 | tooth agenesis | HGNC:12775 | Homo sapiens (human) | 7480 | WNT10B |
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| DOID:14330 | Parkinson's disease | HGNC:11960 | Homo sapiens (human) | 26058 | GIGYF2 |
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| DOID:0081179 | autosomal recessive intellectual developmental disorder 3 | HGNC:30237 | Homo sapiens (human) | 54862 | CC2D1A |
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| DOID:0111498 | combined oxidative phosphorylation deficiency 22 | HGNC:823 | Homo sapiens (human) | 498 | ATP5F1A |
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| DOID:0111298 | familial febrile seizures 8 | HGNC:4087 | Homo sapiens (human) | 2566 | GABRG2 |
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| DOID:0111849 | osteogenesis imperfecta type 20 | HGNC:13520 | Homo sapiens (human) | 23184 | MESD |
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| DOID:0081348 | congenital myopathy 16 | HGNC:7549 | Homo sapiens (human) | 4604 | MYBPC1 |
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| DOID:0111241 | congenital muscular dystrophy-dystroglycanopathy type A5 | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0070262 | congenital disorder of glycosylation type IIj | HGNC:18620 | Homo sapiens (human) | 25839 | COG4 |
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| DOID:0070296 | primary autosomal recessive microcephaly | HGNC:6638 | Homo sapiens (human) | 84823 | LMNB2 |
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| DOID:0111598 | distal arthrogryposis type 1B | HGNC:7549 | Homo sapiens (human) | 4604 | MYBPC1 |
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| DOID:0110698 | hypotrichosis 1 | HGNC:15718 | Homo sapiens (human) | 147495 | APCDD1 |
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| DOID:0070131 | autosomal dominant cutis laxa 3 | HGNC:9722 | Homo sapiens (human) | 5832 | ALDH18A1 |
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| DOID:10123 | pigmentation disease | HGNC:10978 | Homo sapiens (human) | 123041 | SLC24A4 |
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