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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:10605 | short bowel syndrome | HGNC:24039 | Homo sapiens (human) | 79827 | CLMP |
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| DOID:9256 | colorectal cancer | HGNC:3595 | Homo sapiens (human) | 2195 | FAT1 |
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| DOID:0070256 | congenital disorder of glycosylation type IId | HGNC:924 | Homo sapiens (human) | 2683 | B4GALT1 |
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| DOID:3209 | junctional epidermolysis bullosa | HGNC:6490 | Homo sapiens (human) | 3914 | LAMB3 |
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| DOID:2841 | asthma | HGNC:1950 | Homo sapiens (human) | 1128 | CHRM1 |
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| DOID:0112149 | terminal osseous dysplasia | HGNC:3754 | Homo sapiens (human) | 2316 | FLNA |
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| DOID:10907 | microcephaly | HGNC:20766 | Homo sapiens (human) | 7846 | TUBA1A |
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| DOID:0060041 | autism spectrum disorder | HGNC:896 | Homo sapiens (human) | 553 | AVPR1B |
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| DOID:0112382 | muscular dystrophy-dystroglycanopathy type C8 | HGNC:25902 | Homo sapiens (human) | 84892 | POMGNT2 |
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| DOID:0111556 | steatocystoma multiplex | HGNC:6427 | Homo sapiens (human) | 3872 | KRT17 |
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| DOID:0080416 | developmental and epileptic encephalopathy 32 | HGNC:6220 | Homo sapiens (human) | 3737 | KCNA2 |
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| DOID:1909 | melanoma | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:0060180 | colitis | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:1070 | primary open angle glaucoma | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:10763 | hypertension | HGNC:7945 | Homo sapiens (human) | 4883 | NPR3 |
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| DOID:9478 | postpartum depression | HGNC:12008 | Homo sapiens (human) | 7166 | TPH1 |
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| DOID:0080242 | syndromic X-linked mental retardation Hough type | HGNC:19701 | Homo sapiens (human) | 22866 | CNKSR2 |
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| DOID:2671 | transitional cell carcinoma | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:8725 | vascular dementia | HGNC:5232 | Homo sapiens (human) | 3303 | HSPA1A |
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| DOID:0070525 | peeling skin syndrome 6 | HGNC:33276 | Homo sapiens (human) | 388698 | FLG2 |
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| DOID:4948 | gallbladder carcinoma | HGNC:24308 | Homo sapiens (human) | 81037 | CLPTM1L |
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| DOID:5844 | myocardial infarction | HGNC:243 | Homo sapiens (human) | 118 | ADD1 |
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| DOID:0070483 | Watson syndrome | HGNC:7765 | Homo sapiens (human) | 4763 | NF1 |
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| DOID:10892 | hypospadias | HGNC:5218 | Homo sapiens (human) | 3284 | HSD3B2 |
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| DOID:0111433 | optic atrophy 3 | HGNC:8142 | Homo sapiens (human) | 80207 | OPA3 |
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