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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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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:0070371 | leukoencephalopathy with vanishing white matter 4 | HGNC:3260 | Homo sapiens (human) | 8890 | EIF2B4 |
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| DOID:0110242 | cataract 13 with adult i phenotype | HGNC:4204 | Homo sapiens (human) | 2651 | GCNT2 |
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| DOID:0110551 | autosomal dominant nonsyndromic deafness 21 | HGNC:13872 | Homo sapiens (human) | 9750 | RIPOR2 |
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| DOID:12849 | autistic disorder | HGNC:6990 | Homo sapiens (human) | 4204 | MECP2 |
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| DOID:0080857 | primary ovarian insufficiency 1 | HGNC:3775 | Homo sapiens (human) | 2332 | FMR1 |
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| DOID:2316 | brain ischemia | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0060447 | epithelial basement membrane dystrophy | HGNC:11771 | Homo sapiens (human) | 7045 | TGFBI |
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| DOID:12849 | autistic disorder | HGNC:7029 | Homo sapiens (human) | 4233 | MET |
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| DOID:3883 | Lynch syndrome | HGNC:9121 | Homo sapiens (human) | 5378 | PMS1 |
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| DOID:4450 | renal cell carcinoma | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0050424 | familial adenomatous polyposis | HGNC:7527 | Homo sapiens (human) | 4595 | MUTYH |
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| DOID:0050742 | nicotine dependence | HGNC:30287 | Homo sapiens (human) | 57521 | RPTOR |
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| DOID:9146 | visceral leishmaniasis | HGNC:10907 | Homo sapiens (human) | 6556 | SLC11A1 |
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| DOID:0112240 | Leber congenital amaurosis with early-onset deafness | HGNC:20771 | Homo sapiens (human) | 10383 | TUBB4B |
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| DOID:77 | gastrointestinal system disease | HGNC:6990 | Homo sapiens (human) | 4204 | MECP2 |
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| DOID:653 | purine-pyrimidine metabolic disorder | HGNC:12563 | Homo sapiens (human) | 7372 | UMPS |
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| DOID:0080784 | urinary tract infection | HGNC:6026 | Homo sapiens (human) | 3577 | CXCR1 |
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| DOID:9970 | obesity | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:6419 | tetralogy of Fallot | HGNC:9644 | Homo sapiens (human) | 5781 | PTPN11 |
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| DOID:4992 | optic nerve glioma | HGNC:7765 | Homo sapiens (human) | 4763 | NF1 |
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| DOID:0112378 | muscular dystrophy-dystroglycanopathy type B3 | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:9538 | multiple myeloma | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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| DOID:0111134 | focal segmental glomerulosclerosis 9 | HGNC:18688 | Homo sapiens (human) | 286204 | CRB2 |
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| DOID:10825 | essential hypertension | HGNC:7944 | Homo sapiens (human) | 4882 | NPR2 |
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| DOID:9206 | Barrett's esophagus | HGNC:7158 | Homo sapiens (human) | 4321 | MMP12 |
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