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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:9352 | type 2 diabetes mellitus | HGNC:13916 | Homo sapiens (human) | 55937 | APOM |
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| DOID:12662 | paracoccidioidomycosis | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:418 | systemic scleroderma | HGNC:10907 | Homo sapiens (human) | 6556 | SLC11A1 |
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| DOID:0080318 | megalencephalic leukoencephalopathy with subcortical cysts 2A | HGNC:26361 | Homo sapiens (human) | 220296 | HEPACAM |
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| DOID:0050431 | arrhythmogenic right ventricular cardiomyopathy | HGNC:9024 | Homo sapiens (human) | 5318 | PKP2 |
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| DOID:13809 | familial combined hyperlipidemia | HGNC:243 | Homo sapiens (human) | 118 | ADD1 |
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| DOID:0111546 | Currarino syndrome | HGNC:4979 | Homo sapiens (human) | 3110 | MNX1 |
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| DOID:0050453 | lissencephaly | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:10632 | Homo sapiens (human) | 6352 | CCL5 |
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| DOID:13641 | exfoliation syndrome | HGNC:171 | Homo sapiens (human) | 90 | ACVR1 |
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| DOID:1470 | major depressive disorder | HGNC:6929 | Homo sapiens (human) | 4157 | MC1R |
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| DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:10652 | Alzheimer's disease | HGNC:9204 | Homo sapiens (human) | 5444 | PON1 |
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| DOID:0060887 | ossification of the posterior longitudinal ligament of spine | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:0111384 | inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2 | HGNC:5033 | Homo sapiens (human) | 3181 | HNRNPA2B1 |
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| DOID:0110759 | type 1 diabetes mellitus 22 | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
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| DOID:0111492 | combined oxidative phosphorylation deficiency 32 | HGNC:16618 | Homo sapiens (human) | 65993 | MRPS34 |
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| DOID:0060774 | congenital diarrhea | HGNC:16526 | Homo sapiens (human) | 51703 | ACSL5 |
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| DOID:5016 | hepatocellular clear cell carcinoma | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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| DOID:5419 | schizophrenia | HGNC:7884 | Homo sapiens (human) | 4855 | NOTCH4 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:13902 | Homo sapiens (human) | 8710 | SERPINB7 |
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| DOID:0111425 | restrictive cardiomyopathy 1 | HGNC:11947 | Homo sapiens (human) | 7137 | TNNI3 |
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| DOID:3407 | carotid artery disease | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:2893 | cervix carcinoma | HGNC:7059 | Homo sapiens (human) | 4255 | MGMT |
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| DOID:0080381 | nephrotic syndrome type 13 | HGNC:18658 | Homo sapiens (human) | 23165 | NUP205 |
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