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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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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:10283 | prostate cancer | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0081348 | congenital myopathy 16 | HGNC:7549 | Homo sapiens (human) | 4604 | MYBPC1 |
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| DOID:2152 | ovary epithelial cancer | HGNC:16636 | Homo sapiens (human) | 23095 | KIF1B |
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| DOID:0111241 | congenital muscular dystrophy-dystroglycanopathy type A5 | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:5844 | myocardial infarction | HGNC:9204 | Homo sapiens (human) | 5444 | PON1 |
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| DOID:0070262 | congenital disorder of glycosylation type IIj | HGNC:18620 | Homo sapiens (human) | 25839 | COG4 |
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| DOID:11512 | Budd-Chiari syndrome | HGNC:3542 | Homo sapiens (human) | 2153 | F5 |
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| DOID:8893 | psoriasis | HGNC:43 | Homo sapiens (human) | 6890 | TAP1 |
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| DOID:934 | viral infectious disease | HGNC:19191 | Homo sapiens (human) | 81704 | DOCK8 |
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| DOID:784 | chronic kidney disease | HGNC:15633 | Homo sapiens (human) | 54106 | TLR9 |
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| DOID:674 | cleft palate | HGNC:3755 | Homo sapiens (human) | 2317 | FLNB |
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| DOID:12365 | malaria | HGNC:6340 | Homo sapiens (human) | 3813 | KIR3DS1 |
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| DOID:7998 | hyperthyroidism | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:583 | hemolytic anemia | HGNC:8896 | Homo sapiens (human) | 5230 | PGK1 |
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| DOID:0070296 | primary autosomal recessive microcephaly | HGNC:6638 | Homo sapiens (human) | 84823 | LMNB2 |
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| DOID:5522 | basaloid squamous cell carcinoma | HGNC:9585 | Homo sapiens (human) | 5727 | PTCH1 |
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| DOID:0111598 | distal arthrogryposis type 1B | HGNC:7549 | Homo sapiens (human) | 4604 | MYBPC1 |
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| DOID:3068 | glioblastoma | HGNC:6973 | Homo sapiens (human) | 4193 | MDM2 |
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| DOID:0112313 | brain small vessel disease | HGNC:3694 | Homo sapiens (human) | 2266 | FGG |
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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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| DOID:5409 | lung small cell carcinoma | HGNC:795 | Homo sapiens (human) | 472 | ATM |
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| DOID:0080384 | nephrotic syndrome type 6 | HGNC:9678 | Homo sapiens (human) | 5800 | PTPRO |
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| DOID:0081020 | congenital fibrosis of the extraocular muscles 5 | HGNC:18603 | Homo sapiens (human) | 84570 | COL25A1 |
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