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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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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:3910 | lung adenocarcinoma | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:1682 | congenital heart disease | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:4914 | esophagus adenocarcinoma | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:850 | lung disease | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:0060901 | lymphoplasmacytic lymphoma | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:418 | systemic scleroderma | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:0050589 | inflammatory bowel disease | RGD:1562048 | Rattus norvegicus (Norway rat) | 287920 | St6galnac1 |
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| DOID:0080556 | congenital disorder of glycosylation Id | RGD:1306004 | Rattus norvegicus (Norway rat) | 287983 | Alg3 |
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| DOID:5212 | congenital disorder of glycosylation | RGD:1306004 | Rattus norvegicus (Norway rat) | 287983 | Alg3 |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | RGD:1306248 | Rattus norvegicus (Norway rat) | 288091 | Poglut1 |
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| DOID:0080762 | autosomal recessive limb-girdle muscular dystrophy type 2Z | RGD:1306248 | Rattus norvegicus (Norway rat) | 288091 | Poglut1 |
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| DOID:0060256 | Dowling-Degos disease | RGD:1306248 | Rattus norvegicus (Norway rat) | 288091 | Poglut1 |
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| DOID:1793 | pancreatic cancer | RGD:1306727 | Rattus norvegicus (Norway rat) | 288161 | B3galt5 |
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| DOID:7941 | Barrett's adenocarcinoma | HGNC:4559 | Homo sapiens (human) | 2882 | GPX7 |
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| DOID:9206 | Barrett's esophagus | HGNC:4559 | Homo sapiens (human) | 2882 | GPX7 |
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| DOID:684 | hepatocellular carcinoma | RGD:631339 | Rattus norvegicus (Norway rat) | 288583 | Plod3 |
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| DOID:1459 | hypothyroidism | RGD:631339 | Rattus norvegicus (Norway rat) | 288583 | Plod3 |
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| DOID:3649 | pyruvate decarboxylase deficiency | RGD:1359146 | Rattus norvegicus (Norway rat) | 289950 | Pdhb |
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| DOID:0050565 | autosomal recessive nonsyndromic deafness | RGD:1560183 | Rattus norvegicus (Norway rat) | 290501 | Tmtc4 |
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| DOID:0112315 | brain small vessel disease 3 | RGD:1309002 | Rattus norvegicus (Norway rat) | 290637 | Colgalt1 |
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| DOID:0080520 | Tn polyagglutination syndrome | HGNC:24338 | Homo sapiens (human) | 29071 | C1GALT1C1 |
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| DOID:12554 | hemolytic-uremic syndrome | HGNC:24338 | Homo sapiens (human) | 29071 | C1GALT1C1 |
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| DOID:2841 | asthma | HGNC:16037 | Homo sapiens (human) | 29095 | ORMDL2 |
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| DOID:0111230 | congenital muscular dystrophy-dystroglycanopathy type A11 | RGD:1306946 | Rattus norvegicus (Norway rat) | 291212 | B3galnt2 |
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| DOID:0060350 | adenine phosphoribosyltransferase deficiency | RGD:1307758 | Rattus norvegicus (Norway rat) | 292072 | Aprt |
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