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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:9246 | cerebral amyloid angiopathy | HGNC:8133 | Homo sapiens (human) | 4973 | OLR1 |
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| DOID:2945 | severe acute respiratory syndrome | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:10964 | cholesteatoma of middle ear | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:12798 | mucopolysaccharidosis | HGNC:5320 | Homo sapiens (human) | 3373 | HYAL1 |
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| DOID:3407 | carotid artery disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:655 | inherited metabolic disorder | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:0050855 | renal fibrosis | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:1924 | hypogonadism | HGNC:5217 | Homo sapiens (human) | 3283 | HSD3B1 |
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| DOID:10283 | prostate cancer | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:559 | acute pyelonephritis | HGNC:9922 | Homo sapiens (human) | 5950 | RBP4 |
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| DOID:4450 | renal cell carcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:10652 | Alzheimer's disease | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:5844 | myocardial infarction | HGNC:4799 | Homo sapiens (human) | 3033 | HADH |
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| DOID:0060841 | isolated microphthalmia 8 | HGNC:409 | Homo sapiens (human) | 220 | ALDH1A3 |
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| DOID:8719 | in situ carcinoma | HGNC:5467 | Homo sapiens (human) | 3482 | IGF2R |
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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:0060256 | Dowling-Degos disease | HGNC:22954 | Homo sapiens (human) | 56983 | POGLUT1 |
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| DOID:13608 | biliary atresia | HGNC:4250 | Homo sapiens (human) | 2678 | GGT1 |
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| DOID:2913 | acute pancreatitis | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:1062 | Fanconi syndrome | HGNC:11006 | Homo sapiens (human) | 6514 | SLC2A2 |
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| DOID:6000 | congestive heart failure | HGNC:11009 | Homo sapiens (human) | 6517 | SLC2A4 |
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| DOID:11446 | sciatic neuropathy | HGNC:14076 | Homo sapiens (human) | 29956 | CERS2 |
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| DOID:10825 | essential hypertension | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:1287 | cardiovascular system disease | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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