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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:0060000 | infective endocarditis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
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| DOID:0111865 | MEND syndrome | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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| DOID:1936 | atherosclerosis | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:4448 | macular degeneration | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:0050741 | alcohol dependence | HGNC:251 | Homo sapiens (human) | 126 | ADH1C |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:4483 | rhinitis | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:848 | arthritis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:14330 | Parkinson's disease | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0111241 | congenital muscular dystrophy-dystroglycanopathy type A5 | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:9970 | obesity | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:0050877 | pancreatic agenesis | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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| DOID:1380 | endometrial cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0080570 | congenital disorder of glycosylation It | HGNC:8905 | Homo sapiens (human) | 5236 | PGM1 |
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| DOID:0110959 | Gaucher's disease type III | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0110860 | polycystic kidney disease 3 | HGNC:4138 | Homo sapiens (human) | 23193 | GANAB |
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| DOID:9296 | cleft lip | HGNC:10659 | Homo sapiens (human) | 6383 | SDC2 |
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| DOID:0070111 | Niemann-Pick disease type A | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:3153 | lipomatosis | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:10534 | stomach cancer | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:7102 | Homo sapiens (human) | 9562 | MINPP1 |
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| DOID:10952 | nephritis | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:0050424 | familial adenomatous polyposis | HGNC:7527 | Homo sapiens (human) | 4595 | MUTYH |
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| DOID:0050565 | autosomal recessive nonsyndromic deafness | HGNC:25904 | Homo sapiens (human) | 84899 | TMTC4 |
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| DOID:0110297 | autosomal recessive limb-girdle muscular dystrophy type 2K | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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