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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:0080978 | arthrogryposis multiplex congenita-1 | HGNC:18712 | Homo sapiens (human) | 163175 | LGI4 |
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| DOID:0110348 | osteogenesis imperfecta type 12 | HGNC:17321 | Homo sapiens (human) | 121340 | SP7 |
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| DOID:0081030 | central conducting lymphatic anomaly | HGNC:3395 | Homo sapiens (human) | 2050 | EPHB4 |
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| DOID:0081203 | autosomal recessive intellectual developmental disorder 38 | HGNC:4868 | Homo sapiens (human) | 8924 | HERC2 |
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| DOID:0111391 | mucopolysaccharidosis IVA | HGNC:4122 | Homo sapiens (human) | 2588 | GALNS |
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| DOID:11713 | diabetic angiopathy | HGNC:3415 | Homo sapiens (human) | 2056 | EPO |
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| DOID:0111975 | immunodeficiency 44 | HGNC:11363 | Homo sapiens (human) | 6773 | STAT2 |
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| DOID:0050591 | tooth agenesis | HGNC:3157 | Homo sapiens (human) | 1896 | EDA |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0070387 | developmental and epileptic encephalopathy 101 | HGNC:4584 | Homo sapiens (human) | 2902 | GRIN1 |
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| DOID:0070273 | hereditary nonpolyposis colorectal cancer type 6 | HGNC:11773 | Homo sapiens (human) | 7048 | TGFBR2 |
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| DOID:0111263 | combined malonic and methylmalonic acidemia | HGNC:27288 | Homo sapiens (human) | 197322 | ACSF3 |
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| DOID:0110460 | dilated cardiomyopathy 2A | HGNC:11947 | Homo sapiens (human) | 7137 | TNNI3 |
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| DOID:0070235 | Loeys-Dietz syndrome 1 | HGNC:11772 | Homo sapiens (human) | 7046 | TGFBR1 |
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| DOID:0070432 | hyperphosphatasia with impaired intellectual development syndrome 5 | HGNC:23213 | Homo sapiens (human) | 284098 | PIGW |
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| DOID:0110880 | holoprosencephaly 4 | HGNC:11776 | Homo sapiens (human) | 7050 | TGIF1 |
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| DOID:0080527 | bronchiectasis 2 | HGNC:10599 | Homo sapiens (human) | 6337 | SCNN1A |
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| DOID:0080694 | Galloway-Mowat syndrome | HGNC:29914 | Homo sapiens (human) | 57122 | NUP107 |
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| DOID:13777 | epidermodysplasia verruciformis | HGNC:20474 | Homo sapiens (human) | 147138 | TMC8 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:12303 | Homo sapiens (human) | 7204 | TRIO |
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| DOID:0050650 | familial atrial fibrillation | HGNC:6242 | Homo sapiens (human) | 9992 | KCNE2 |
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| DOID:0112035 | non-syndromic X-linked intellectual disability 96 | HGNC:11506 | Homo sapiens (human) | 6855 | SYP |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:10914 | Homo sapiens (human) | 9990 | SLC12A6 |
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| DOID:0110704 | hypotrichosis 7 | HGNC:18483 | Homo sapiens (human) | 200879 | LIPH |
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| DOID:0080738 | Ehlers-Danlos syndrome spondylodysplastic type 1 | HGNC:930 | Homo sapiens (human) | 11285 | B4GALT7 |
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