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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:14500 | fucosidosis | HGNC:4006 | Homo sapiens (human) | 2517 | FUCA1 |
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| DOID:0111041 | glycogen storage disease IXb | HGNC:8927 | Homo sapiens (human) | 5257 | PHKB |
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| DOID:0060537 | mitochondrial complex II deficiency | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:12716 | newborn respiratory distress syndrome | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:10908 | hydrocephalus | HGNC:6470 | Homo sapiens (human) | 3897 | L1CAM |
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| DOID:0050811 | congenital adrenal hyperplasia | HGNC:2591 | Homo sapiens (human) | 1584 | CYP11B1 |
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| DOID:2842 | Jervell-Lange Nielsen syndrome | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:1612 | breast cancer | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:0090101 | lethal congenital glycogen storage disease of heart | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:2843 | long QT syndrome | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:9743 | diabetic neuropathy | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0111459 | classic galactosemia | HGNC:4135 | Homo sapiens (human) | 2592 | GALT |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:0110191 | Charcot-Marie-Tooth disease type 4B1 | HGNC:7450 | Homo sapiens (human) | 8898 | MTMR2 |
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| DOID:0110011 | advanced sleep phase syndrome 1 | HGNC:8846 | Homo sapiens (human) | 8864 | PER2 |
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| DOID:0080197 | congenital muscular dystrophy with cataracts and intellectual disability | HGNC:33882 | Homo sapiens (human) | 51763 | INPP5K |
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| DOID:0060589 | Yunis-Varon syndrome | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0111277 | mitochondrial trifunctional protein deficiency | HGNC:4803 | Homo sapiens (human) | 3032 | HADHB |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:0050883 | infantile cerebellar-retinal degeneration | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:0110957 | Gaucher's disease type I | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:9352 | type 2 diabetes mellitus | RGD:3001 | Rattus norvegicus (Norway rat) | 24536 | Lepr |
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| DOID:12803 | Sly syndrome | HGNC:4696 | Homo sapiens (human) | 2990 | GUSB |
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