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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:10584 | retinitis pigmentosa | HGNC:29253 | Homo sapiens (human) | 57545 | CC2D2A |
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| DOID:0070482 | spinal neurofibromatosis | HGNC:7765 | Homo sapiens (human) | 4763 | NF1 |
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| DOID:0070405 | hypomyelinating leukodystrophy 16 | HGNC:22407 | Homo sapiens (human) | 54664 | TMEM106B |
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| DOID:6039 | uveal melanoma | HGNC:6919 | Homo sapiens (human) | 8930 | MBD4 |
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| DOID:0112026 | non-syndromic X-linked intellectual disability 99 | HGNC:12632 | Homo sapiens (human) | 8239 | USP9X |
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| DOID:0111916 | spermatogenic failure 28 | HGNC:23168 | Homo sapiens (human) | 57697 | FANCM |
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| DOID:0080663 | atrial standstill 2 | HGNC:7939 | Homo sapiens (human) | 4878 | NPPA |
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| DOID:0111854 | primary ciliary dyskinesia 39 | HGNC:25430 | Homo sapiens (human) | 115399 | LRRC56 |
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| DOID:5426 | primary ovarian insufficiency | HGNC:26520 | Homo sapiens (human) | 147872 | KASH5 |
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| DOID:0112319 | Kanzaki disease | HGNC:7631 | Homo sapiens (human) | 4668 | NAGA |
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| DOID:0112140 | retinitis pigmentosa 83 | HGNC:694 | Homo sapiens (human) | 403 | ARL3 |
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| DOID:2340 | craniosynostosis | HGNC:450 | Homo sapiens (human) | 60529 | ALX4 |
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| DOID:0112271 | spermatogenic failure 49 | HGNC:26676 | Homo sapiens (human) | 159686 | CFAP58 |
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| DOID:12978 | Plasmodium vivax malaria | HGNC:4035 | Homo sapiens (human) | 2532 | ACKR1 |
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| DOID:0081365 | Paget's disease of bone 2 | HGNC:11908 | Homo sapiens (human) | 8792 | TNFRSF11A |
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| DOID:0112196 | spondylometaepiphyseal dysplasia, short limb-hand type | HGNC:2731 | Homo sapiens (human) | 4921 | DDR2 |
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| DOID:2043 | hepatitis B | HGNC:5433 | Homo sapiens (human) | 3455 | IFNAR2 |
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| DOID:0050540 | Charcot-Marie-Tooth disease type 3 | HGNC:3239 | Homo sapiens (human) | 1959 | EGR2 |
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| DOID:0050650 | familial atrial fibrillation | HGNC:7939 | Homo sapiens (human) | 4878 | NPPA |
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| DOID:13189 | gout | HGNC:10931 | Homo sapiens (human) | 10786 | SLC17A3 |
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| DOID:0110066 | amelogenesis imperfecta type 1G | HGNC:23015 | Homo sapiens (human) | 54757 | FAM20A |
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| DOID:0080576 | spondyloepimetaphyseal dysplasia, Genevieve-type | HGNC:19237 | Homo sapiens (human) | 54187 | NANS |
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| DOID:0060584 | Noonan syndrome 6 | HGNC:7989 | Homo sapiens (human) | 4893 | NRAS |
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| DOID:0080470 | developmental and epileptic encephalopathy 36 | HGNC:30881 | Homo sapiens (human) | 79868 | ALG13 |
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| DOID:0110384 | retinitis pigmentosa 25 | HGNC:21555 | Homo sapiens (human) | 346007 | EYS |
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