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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:1826 | epilepsy | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:0111156 | spermatogenic failure 9 | HGNC:19414 | Homo sapiens (human) | 283417 | DPY19L2 |
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| DOID:0081419 | childhood-onset dystonia with optic atrophy and basal ganglia abnormalities | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
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| DOID:0111756 | Leber hereditary optic neuropathy with demyelinating disease of CNS | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
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| DOID:5723 | optic atrophy | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
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| DOID:5419 | schizophrenia | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
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| DOID:2256 | osteochondrodysplasia | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
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| DOID:0050813 | spondyloepiphyseal dysplasia with congenital joint dislocations | HGNC:1971 | Homo sapiens (human) | 9469 | CHST3 |
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| DOID:0111240 | congenital muscular dystrophy-dystroglycanopathy type A2 | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0112374 | muscular dystrophy-dystroglycanopathy | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:9884 | muscular dystrophy | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0110298 | autosomal recessive limb-girdle muscular dystrophy type 2N | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0112380 | muscular dystrophy-dystroglycanopathy type B2 | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0050453 | lissencephaly | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:9256 | colorectal cancer | HGNC:19877 | Homo sapiens (human) | 79695 | GALNT12 |
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| DOID:0060230 | basal ganglia calcification | HGNC:19918 | Homo sapiens (human) | 57462 | MYORG |
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| DOID:162 | cancer | HGNC:19980 | Homo sapiens (human) | 64841 | GNPNAT1 |
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| DOID:0080753 | keratosis follicularis spinulosa decalvans | HGNC:19980 | Homo sapiens (human) | 64841 | GNPNAT1 |
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| DOID:9970 | obesity | HGNC:20113 | Homo sapiens (human) | 123099 | DEGS2 |
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| DOID:1289 | neurodegenerative disease | HGNC:20113 | Homo sapiens (human) | 123099 | DEGS2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:20147 | Homo sapiens (human) | 51167 | CYB5R4 |
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| DOID:0081312 | T-cell non-Hodgkin lymphoma | HGNC:20185 | Homo sapiens (human) | 54916 | TMEM260 |
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| DOID:10534 | stomach cancer | HGNC:20185 | Homo sapiens (human) | 54916 | TMEM260 |
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