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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0080155 | very long chain acyl-CoA dehydrogenase deficiency | HGNC:92 | Homo sapiens (human) | 37 | ACADVL |
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| DOID:783 | end stage renal disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:11612 | polycystic ovary syndrome | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:0060233 | cardiofaciocutaneous syndrome | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:0110480 | autosomal recessive nonsyndromic deafness 22 | HGNC:16378 | Homo sapiens (human) | 146183 | OTOA |
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| DOID:13832 | patent ductus arteriosus | HGNC:11743 | Homo sapiens (human) | 7021 | TFAP2B |
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| DOID:0110632 | megaconial type congenital muscular dystrophy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:783 | end stage renal disease | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:14330 | Parkinson's disease | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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| DOID:0111330 | combined saposin deficiency | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:14118 | familial lipoprotein lipase deficiency | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:14504 | Niemann-Pick disease | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:1168 | familial hyperlipidemia | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:5844 | myocardial infarction | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:850 | lung disease | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:20147 | Homo sapiens (human) | 51167 | CYB5R4 |
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| DOID:10763 | hypertension | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0060202 | amyotrophic lateral sclerosis type 11 | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0110858 | polycystic kidney disease 1 | HGNC:9008 | Homo sapiens (human) | 5310 | PKD1 |
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| DOID:0070255 | congenital disorder of glycosylation type IIc | HGNC:20197 | Homo sapiens (human) | 55343 | SLC35C1 |
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| DOID:3322 | GM1 gangliosidosis | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:10763 | hypertension | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:10581 | metachromatic leukodystrophy | HGNC:713 | Homo sapiens (human) | 410 | ARSA |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9235 | Homo sapiens (human) | 5467 | PPARD |
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