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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:0081075 | Marsili syndrome | HGNC:20152 | Homo sapiens (human) | 85446 | ZFHX2 |
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| DOID:9743 | diabetic neuropathy | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:9970 | obesity | HGNC:644 | Homo sapiens (human) | 367 | AR |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11289 | Homo sapiens (human) | 6720 | SREBF1 |
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| DOID:9970 | obesity | HGNC:3023 | Homo sapiens (human) | 1813 | DRD2 |
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| DOID:0070473 | Zaki syndrome | HGNC:30238 | Homo sapiens (human) | 79971 | WLS |
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| DOID:0060537 | mitochondrial complex II deficiency | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:0050545 | visceral heterotaxy | HGNC:26530 | Homo sapiens (human) | 220136 | CFAP53 |
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| DOID:0111089 | Fanconi anemia complementation group D1 | HGNC:1101 | Homo sapiens (human) | 675 | BRCA2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:3091 | Homo sapiens (human) | 1859 | DYRK1A |
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| DOID:2732 | Rothmund-Thomson syndrome | HGNC:9949 | Homo sapiens (human) | 9401 | RECQL4 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11621 | Homo sapiens (human) | 6927 | HNF1A |
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| DOID:0110844 | xeroderma pigmentosum group C | HGNC:12816 | Homo sapiens (human) | 7508 | XPC |
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| DOID:0081175 | short stature, hearing loss, retinitis pigmentosa, and distinctive facies | HGNC:17097 | Homo sapiens (human) | 23404 | EXOSC2 |
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| DOID:14720 | Ehlers-Danlos syndrome classic type 1 | HGNC:2209 | Homo sapiens (human) | 1289 | COL5A1 |
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| DOID:0090116 | spondylocarpotarsal synostosis syndrome | HGNC:3755 | Homo sapiens (human) | 2317 | FLNB |
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| DOID:1935 | Bardet-Biedl syndrome | HGNC:20087 | Homo sapiens (human) | 123016 | TTC8 |
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| DOID:0090067 | Fuhrmann syndrome | HGNC:12786 | Homo sapiens (human) | 7476 | WNT7A |
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| DOID:0110342 | osteogenesis imperfecta type 13 | HGNC:1067 | Homo sapiens (human) | 649 | BMP1 |
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| DOID:0111138 | congenital generalized lipodystrophy type 4 | HGNC:9688 | Homo sapiens (human) | 284119 | CAVIN1 |
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| DOID:12347 | osteogenesis imperfecta | HGNC:2198 | Homo sapiens (human) | 1278 | COL1A2 |
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| DOID:0111725 | geleophysic dysplasia 1 | HGNC:14631 | Homo sapiens (human) | 9719 | ADAMTSL2 |
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| DOID:0110970 | brachydactyly type C | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0111206 | autosomal dominant distal hereditary motor neuronopathy 2 | HGNC:30171 | Homo sapiens (human) | 26353 | HSPB8 |
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| DOID:12803 | Sly syndrome | HGNC:4696 | Homo sapiens (human) | 2990 | GUSB |
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