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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:12930 | dilated cardiomyopathy | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:0050852 | limb ischemia | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:7998 | hyperthyroidism | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:1459 | hypothyroidism | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:8466 | retinal degeneration | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:3312 | bipolar disorder | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:6000 | congestive heart failure | HGNC:2422 | Homo sapiens (human) | 1431 | CS |
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| DOID:0111141 | delayed sleep phase syndrome | HGNC:2384 | Homo sapiens (human) | 1407 | CRY1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:27301 | Homo sapiens (human) | 200186 | CRTC2 |
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| DOID:0110295 | autosomal recessive limb-girdle muscular dystrophy type 2U | HGNC:37276 | Homo sapiens (human) | 729920 | CRPPA |
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| DOID:0111234 | congenital muscular dystrophy-dystroglycanopathy A7 | HGNC:37276 | Homo sapiens (human) | 729920 | CRPPA |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:37276 | Homo sapiens (human) | 729920 | CRPPA |
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| DOID:0070430 | combined oxidative phosphorylation deficiency 57 | HGNC:16148 | Homo sapiens (human) | 54675 | CRLS1 |
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| DOID:0080000 | muscular disease | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
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| DOID:0080000 | muscular disease | FB:FBgn0035383 | Drosophila melanogaster (fruit fly) | 38355 | CPT2 |
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| DOID:936 | brain disease | FB:FBgn0035383 | Drosophila melanogaster (fruit fly) | 38355 | CPT2 |
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| DOID:3146 | lipid metabolism disorder | FB:FBgn0035383 | Drosophila melanogaster (fruit fly) | 38355 | CPT2 |
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| DOID:936 | brain disease | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
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| DOID:3146 | lipid metabolism disorder | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
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| DOID:0110818 | hereditary spastic paraplegia 73 | HGNC:18540 | Homo sapiens (human) | 126129 | CPT1C |
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| DOID:0090129 | carnitine palmitoyltransferase I deficiency | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:9970 | obesity | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:3319 | lymphangioleiomyomatosis | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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