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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:8398 | osteoarthritis | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:9970 | obesity | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:0060887 | ossification of the posterior longitudinal ligament of spine | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:0050644 | arterial calcification of infancy | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:1214 | tympanosclerosis | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:10754 | otitis media | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:13207 | proliferative diabetic retinopathy | HGNC:3357 | Homo sapiens (human) | 5168 | ENPP2 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:33882 | Homo sapiens (human) | 51763 | INPP5K |
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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:3393 | coronary artery disease | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:13810 | familial hypercholesterolemia | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:3526 | cerebral infarction | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:6432 | pulmonary hypertension | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:10763 | hypertension | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:14330 | Parkinson's disease | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:0111670 | primary hyperoxaluria type 1 | HGNC:341 | Homo sapiens (human) | 189 | AGXT |
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| DOID:2977 | primary hyperoxaluria | HGNC:341 | Homo sapiens (human) | 189 | AGXT |
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| DOID:891 | progressive myoclonus epilepsy | HGNC:3413 | Homo sapiens (human) | 7957 | EPM2A |
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| DOID:3534 | Lafora disease | HGNC:3413 | Homo sapiens (human) | 7957 | EPM2A |
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| DOID:0060041 | autism spectrum disorder | HGNC:3512 | Homo sapiens (human) | 2131 | EXT1 |
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| DOID:206 | hereditary multiple exostoses | HGNC:3512 | Homo sapiens (human) | 2131 | EXT1 |
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| DOID:3371 | chondrosarcoma | HGNC:3512 | Homo sapiens (human) | 2131 | EXT1 |
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| DOID:206 | hereditary multiple exostoses | HGNC:3513 | Homo sapiens (human) | 2132 | EXT2 |
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| DOID:206 | hereditary multiple exostoses | HGNC:3515 | Homo sapiens (human) | 2134 | EXTL1 |
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