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GlyTouCan
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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▲ |
|---|---|---|---|---|---|---|---|---|
| DOID:0070288 | primary autosomal recessive microcephaly 17 | HGNC:1985 | Homo sapiens (human) | 11113 | CIT |
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| DOID:0060213 | frontotemporal dementia and/or amyotrophic lateral sclerosis 1 | HGNC:28337 | Homo sapiens (human) | 203228 | C9orf72 |
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| DOID:0070261 | congenital disorder of glycosylation type IIi | HGNC:14857 | Homo sapiens (human) | 10466 | COG5 |
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| DOID:0080923 | bilateral parasagittal parieto-occipital polymicrogyria | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0081333 | Wiedemann-Rautenstrauch syndrome | HGNC:30074 | Homo sapiens (human) | 11128 | POLR3A |
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| DOID:0060302 | type II complement component 8 deficiency | HGNC:1353 | Homo sapiens (human) | 732 | C8B |
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| DOID:0050816 | urofacial syndrome | HGNC:20889 | Homo sapiens (human) | 9860 | LRIG2 |
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| DOID:0070466 | carpal tunnel syndrome 1 | HGNC:12405 | Homo sapiens (human) | 7276 | TTR |
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| DOID:5683 | hereditary breast ovarian cancer syndrome | HGNC:26144 | Homo sapiens (human) | 79728 | PALB2 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:6120 | Homo sapiens (human) | 3663 | IRF5 |
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| DOID:9256 | colorectal cancer | HGNC:8805 | Homo sapiens (human) | 5157 | PDGFRL |
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| DOID:0060668 | anencephaly | HGNC:29558 | Homo sapiens (human) | 81788 | NUAK2 |
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| DOID:11830 | myopia | HGNC:29222 | Homo sapiens (human) | 84146 | ZNF644 |
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| DOID:0111243 | acromicric dysplasia | HGNC:3603 | Homo sapiens (human) | 2200 | FBN1 |
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| DOID:4586 | familial meningioma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:0110021 | age related macular degeneration 9 | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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| DOID:0111432 | essential tremor 5 | HGNC:29945 | Homo sapiens (human) | 26011 | TENM4 |
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| DOID:0111352 | D-2-hydroxyglutaric aciduria 2 | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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| DOID:0111837 | congenital nongoitrous hypothyroidism 8 | HGNC:11585 | Homo sapiens (human) | 6907 | TBL1X |
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| DOID:10591 | pre-eclampsia | HGNC:19012 | Homo sapiens (human) | 10699 | CORIN |
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| DOID:0081381 | juvenile amyotrophic lateral sclerosis type 27 | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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| DOID:10123 | pigmentation disease | HGNC:8101 | Homo sapiens (human) | 4948 | OCA2 |
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| DOID:0111508 | Torrance type platyspondylic dysplasia | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:2366 | West Nile fever | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
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| DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:7516 | Homo sapiens (human) | 727897 | MUC5B |
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