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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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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:0060668 | anencephaly | HGNC:29168 | Homo sapiens (human) | 23322 | RPGRIP1L |
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| DOID:0080560 | congenital disorder of glycosylation Ih | HGNC:23161 | Homo sapiens (human) | 79053 | ALG8 |
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| DOID:11342 | arcus senilis | HGNC:6309 | Homo sapiens (human) | 11081 | KERA |
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| DOID:10223 | dermatomyositis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0111059 | Bernard-Soulier syndrome type A2 | HGNC:4439 | Homo sapiens (human) | 2811 | GP1BA |
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| DOID:0111310 | familial febrile seizures 2 | HGNC:4846 | Homo sapiens (human) | 610 | HCN2 |
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| DOID:401 | multidrug-resistant tuberculosis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:12798 | mucopolysaccharidosis | HGNC:5320 | Homo sapiens (human) | 3373 | HYAL1 |
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| DOID:61 | mitral valve disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:1909 | melanoma | HGNC:7794 | Homo sapiens (human) | 4790 | NFKB1 |
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| DOID:9007 | sudden infant death syndrome | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:11621 | Homo sapiens (human) | 6927 | HNF1A |
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| DOID:1068 | juvenile glaucoma | HGNC:7610 | Homo sapiens (human) | 4653 | MYOC |
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| DOID:0060571 | Ritscher-Schinzel syndrome 1 | HGNC:28984 | Homo sapiens (human) | 9897 | WASHC5 |
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| DOID:0111415 | trichohepatoenteric syndrome 1 | HGNC:23639 | Homo sapiens (human) | 9652 | SKIC3 |
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| DOID:612 | primary immunodeficiency disease | HGNC:3573 | Homo sapiens (human) | 8772 | FADD |
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| DOID:0060836 | isolated microphthalmia 4 | HGNC:4221 | Homo sapiens (human) | 392255 | GDF6 |
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| DOID:988 | mitral valve prolapse | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:1930 | Laurence-Moon syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:583 | hemolytic anemia | HGNC:5141 | Homo sapiens (human) | 3240 | HP |
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| DOID:0070133 | autosomal recessive cutis laxa type IB | HGNC:3219 | Homo sapiens (human) | 30008 | EFEMP2 |
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| DOID:3393 | coronary artery disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:4465 | papillary renal cell carcinoma | HGNC:9343 | Homo sapiens (human) | 5546 | PRCC |
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| DOID:104 | bacterial infectious disease | HGNC:19191 | Homo sapiens (human) | 81704 | DOCK8 |
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| DOID:4450 | renal cell carcinoma | HGNC:1323 | Homo sapiens (human) | 720 | C4A |
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