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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:13378 | Kawasaki disease | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:0070399 | hypomyelinating leukodystrophy 18 | HGNC:13709 | Homo sapiens (human) | 8560 | DEGS1 |
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| DOID:9970 | obesity | HGNC:13709 | Homo sapiens (human) | 8560 | DEGS1 |
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| DOID:1289 | neurodegenerative disease | HGNC:13709 | Homo sapiens (human) | 8560 | DEGS1 |
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| DOID:0060786 | hypomyelinating leukodystrophy | HGNC:13709 | Homo sapiens (human) | 8560 | DEGS1 |
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| DOID:10584 | retinitis pigmentosa | HGNC:1375 | Homo sapiens (human) | 762 | CA4 |
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| DOID:0070395 | developmental and epileptic encephalopathy 110 | HGNC:1399 | Homo sapiens (human) | 781 | CACNA2D1 |
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| DOID:3454 | brain infarction | HGNC:1399 | Homo sapiens (human) | 781 | CACNA2D1 |
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| DOID:1826 | epilepsy | HGNC:1400 | Homo sapiens (human) | 9254 | CACNA2D2 |
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| DOID:11446 | sciatic neuropathy | HGNC:14076 | Homo sapiens (human) | 29956 | CERS2 |
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| DOID:0112213 | multiple congenital anomalies-hypotonia-seizures syndrome 4 | HGNC:14135 | Homo sapiens (human) | 9091 | PIGQ |
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| DOID:14735 | hereditary angioedema | HGNC:14178 | Homo sapiens (human) | 64711 | HS3ST6 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:0110339 | osteogenesis imperfecta type 3 | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:9675 | pulmonary emphysema | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:12347 | osteogenesis imperfecta | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:6432 | pulmonary hypertension | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:0110341 | osteogenesis imperfecta type 2 | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:9406 | hypopituitarism | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:224 | transient cerebral ischemia | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:0111451 | progressive myoclonus epilepsy 8 | HGNC:14253 | Homo sapiens (human) | 10715 | CERS1 |
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| DOID:2566 | corneal dystrophy | HGNC:14415 | Homo sapiens (human) | 6785 | ELOVL4 |
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| DOID:0050817 | Stargardt disease | HGNC:14415 | Homo sapiens (human) | 6785 | ELOVL4 |
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| DOID:0050981 | spinocerebellar ataxia type 34 | HGNC:14415 | Homo sapiens (human) | 6785 | ELOVL4 |
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| DOID:10588 | adrenoleukodystrophy | HGNC:14418 | Homo sapiens (human) | 64834 | ELOVL1 |
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