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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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Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▲ |
|---|---|---|---|---|---|---|---|---|
| DOID:0112158 | De Sanctis-Cacchione syndrome | HGNC:3438 | Homo sapiens (human) | 2074 | ERCC6 |
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| DOID:0111469 | combined oxidative phosphorylation deficiency 16 | HGNC:16650 | Homo sapiens (human) | 65080 | MRPL44 |
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| DOID:0111974 | immunodeficiency 59 | HGNC:16931 | Homo sapiens (human) | 10525 | HYOU1 |
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| DOID:0111418 | familial apolipoprotein C-II deficiency | HGNC:609 | Homo sapiens (human) | 344 | APOC2 |
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| DOID:5844 | myocardial infarction | HGNC:9535 | Homo sapiens (human) | 5687 | PSMA6 |
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| DOID:0110823 | hereditary spastic paraplegia 8 | HGNC:28984 | Homo sapiens (human) | 9897 | WASHC5 |
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| DOID:0110727 | neuronal ceroid lipofuscinosis 13 | HGNC:2531 | Homo sapiens (human) | 8722 | CTSF |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:17382 | Homo sapiens (human) | 57522 | SRGAP1 |
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| DOID:0060912 | craniosynostosis 7 | HGNC:6772 | Homo sapiens (human) | 4091 | SMAD6 |
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| DOID:0112150 | X-linked spondyloepimetaphyseal dysplasia | HGNC:1044 | Homo sapiens (human) | 633 | BGN |
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| DOID:0111162 | epidermal nevus | HGNC:3690 | Homo sapiens (human) | 2261 | FGFR3 |
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| DOID:0111061 | familial hypobetalipoproteinemia 2 | HGNC:491 | Homo sapiens (human) | 27329 | ANGPTL3 |
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| DOID:0110674 | congenital myasthenic syndrome 17 | HGNC:6696 | Homo sapiens (human) | 4038 | LRP4 |
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| DOID:0070374 | leukoencephalopathy with vanishing white matter 1 | HGNC:3257 | Homo sapiens (human) | 1967 | EIF2B1 |
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| DOID:9649 | congenital nystagmus | HGNC:10249 | Homo sapiens (human) | 6091 | ROBO1 |
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| DOID:612 | primary immunodeficiency disease | HGNC:15879 | Homo sapiens (human) | 56259 | CTNNBL1 |
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| DOID:0110839 | Usher syndrome type 2C | HGNC:26257 | Homo sapiens (human) | 79955 | PDZD7 |
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| DOID:0081137 | agammaglobulinemia 3 | HGNC:1698 | Homo sapiens (human) | 973 | CD79A |
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| DOID:0081180 | autosomal recessive intellectual developmental disorder 12 | HGNC:10866 | Homo sapiens (human) | 6487 | ST3GAL3 |
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| DOID:0111901 | heparin cofactor II deficiency | HGNC:4838 | Homo sapiens (human) | 3053 | SERPIND1 |
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| DOID:0110574 | autosomal dominant nonsyndromic deafness 4B | HGNC:31948 | Homo sapiens (human) | 388551 | CEACAM16 |
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| DOID:0060718 | autosomal recessive congenital ichthyosis 9 | HGNC:23752 | Homo sapiens (human) | 204219 | CERS3 |
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| DOID:0111314 | idiopathic generalized epilepsy 13 | HGNC:4075 | Homo sapiens (human) | 2554 | GABRA1 |
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| DOID:12271 | aniridia | HGNC:1171 | Homo sapiens (human) | 26610 | ELP4 |
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| DOID:6419 | tetralogy of Fallot | HGNC:4173 | Homo sapiens (human) | 2626 | GATA4 |
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