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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:0070451 | mitochondrial DNA depletion syndrome 20 | HGNC:6600 | Homo sapiens (human) | 3980 | LIG3 |
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| DOID:0080845 | omodysplasia 2 | HGNC:4040 | Homo sapiens (human) | 2535 | FZD2 |
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| DOID:0112143 | retinitis pigmentosa 86 | HGNC:22219 | Homo sapiens (human) | 57670 | KIAA1549 |
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| DOID:0050545 | visceral heterotaxy | HGNC:4214 | Homo sapiens (human) | 2657 | GDF1 |
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| DOID:0050793 | short QT syndrome | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:0080432 | developmental and epileptic encephalopathy 60 | HGNC:11968 | Homo sapiens (human) | 10695 | CNPY3 |
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| DOID:0050719 | cerebral folate receptor alpha deficiency | HGNC:3791 | Homo sapiens (human) | 2348 | FOLR1 |
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| DOID:11949 | Creutzfeldt-Jakob disease | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:612 | primary immunodeficiency disease | HGNC:5432 | Homo sapiens (human) | 3454 | IFNAR1 |
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| DOID:0080331 | cold-induced sweating syndrome 3 | HGNC:15646 | Homo sapiens (human) | 55975 | KLHL7 |
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| DOID:0050651 | atrioventricular septal defect | HGNC:14630 | Homo sapiens (human) | 78987 | CRELD1 |
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| DOID:0080019 | metaphyseal dysplasia | HGNC:10778 | Homo sapiens (human) | 6424 | SFRP4 |
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| DOID:0060558 | lethal congenital contracture syndrome | HGNC:2974 | Homo sapiens (human) | 1785 | DNM2 |
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| DOID:0110607 | primary ciliary dyskinesia 28 | HGNC:11212 | Homo sapiens (human) | 6674 | SPAG1 |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:4396 | Homo sapiens (human) | 2782 | GNB1 |
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| DOID:0060309 | syndromic X-linked intellectual disability | HGNC:2745 | Homo sapiens (human) | 1654 | DDX3X |
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| DOID:0111233 | congenital muscular dystrophy-dystroglycanopathy A14 | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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| DOID:0070058 | Helsmoortel-Van Der Aa Syndrome | HGNC:15766 | Homo sapiens (human) | 23394 | ADNP |
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| DOID:0110042 | Alzheimer's disease 3 | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:0080488 | mucolipidosis | HGNC:7758 | Homo sapiens (human) | 4758 | NEU1 |
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| DOID:0060558 | lethal congenital contracture syndrome | HGNC:18591 | Homo sapiens (human) | 91754 | NEK9 |
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| DOID:0080353 | X-linked recessive hypophosphatemic rickets | HGNC:2023 | Homo sapiens (human) | 1184 | CLCN5 |
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| DOID:0080272 | nephrotic syndrome type 16 | HGNC:29300 | Homo sapiens (human) | 25959 | KANK2 |
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| DOID:0112104 | Sotos syndrome 3 | HGNC:24036 | Homo sapiens (human) | 10297 | APC2 |
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| DOID:0110909 | inflammatory bowel disease 25 | HGNC:5965 | Homo sapiens (human) | 3588 | IL10RB |
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