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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:0080886 | vitamin D-dependent rickets type 1A | HGNC:2606 | Homo sapiens (human) | 1594 | CYP27B1 |
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| DOID:0111071 | congenital bile acid synthesis defect 1 | HGNC:18324 | Homo sapiens (human) | 80270 | HSD3B7 |
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| DOID:0050813 | spondyloepiphyseal dysplasia with congenital joint dislocations | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
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| DOID:0112072 | nuclear type mitochondrial complex I deficiency 20 | HGNC:88 | Homo sapiens (human) | 33 | ACADL |
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| DOID:0050912 | colon adenoma | HGNC:1937 | Homo sapiens (human) | 1119 | CHKA |
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| DOID:2738 | pseudoxanthoma elasticum | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:13241 | Behcet's disease | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:0050534 | congenital stationary night blindness | HGNC:8082 | Homo sapiens (human) | 60506 | NYX |
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| DOID:0050426 | Stevens-Johnson syndrome | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0060537 | mitochondrial complex II deficiency | HGNC:10683 | Homo sapiens (human) | 6392 | SDHD |
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| DOID:0060363 | glycerol kinase deficiency | HGNC:4291 | Homo sapiens (human) | 2712 | GK2 |
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| DOID:1059 | intellectual disability | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:9452 | steatotic liver disease | HGNC:4250 | Homo sapiens (human) | 2678 | GGT1 |
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| DOID:4467 | clear cell renal cell carcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:10763 | hypertension | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:6543 | acne | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:1240 | leukemia | HGNC:16496 | Homo sapiens (human) | 23305 | ACSL6 |
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| DOID:1273 | respiratory syncytial virus infectious disease | HGNC:10802 | Homo sapiens (human) | 6440 | SFTPC |
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| DOID:5844 | myocardial infarction | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:13372 | alpha 1-antitrypsin deficiency | HGNC:18359 | Homo sapiens (human) | 145264 | SERPINA12 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2705 | Homo sapiens (human) | 1634 | DCN |
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| DOID:6000 | congestive heart failure | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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