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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:0060870 | isolated growth hormone deficiency | RGD:2688 | Rattus norvegicus (Norway rat) | 25321 | Ghrhr |
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| DOID:0110839 | Usher syndrome type 2C | HGNC:17416 | Homo sapiens (human) | 84059 | ADGRV1 |
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| DOID:11832 | visual epilepsy | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:12388 | neurohypophyseal diabetes insipidus | HGNC:894 | Homo sapiens (human) | 551 | AVP |
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| DOID:0050752 | amyotrophic lateral sclerosis type 8 | HGNC:12649 | Homo sapiens (human) | 9217 | VAPB |
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| DOID:0060610 | megacystis-microcolon-intestinal hypoperistalsis syndrome | HGNC:7569 | Homo sapiens (human) | 4629 | MYH11 |
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| DOID:0060473 | Kabuki syndrome | HGNC:7133 | Homo sapiens (human) | 8085 | KMT2D |
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| DOID:1574 | alcohol use disorder | HGNC:8153 | Homo sapiens (human) | 4985 | OPRD1 |
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| DOID:0080562 | congenital disorder of glycosylation Ij | HGNC:2995 | Homo sapiens (human) | 1798 | DPAGT1 |
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| DOID:1060 | Hartnup disease | HGNC:27960 | Homo sapiens (human) | 340024 | SLC6A19 |
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| DOID:11612 | polycystic ovary syndrome | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:14731 | Weaver syndrome | HGNC:3527 | Homo sapiens (human) | 2146 | EZH2 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:9016 | Homo sapiens (human) | 5314 | PKHD1 |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:8806 | Homo sapiens (human) | 5160 | PDHA1 |
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| DOID:4483 | rhinitis | HGNC:5973 | Homo sapiens (human) | 3596 | IL13 |
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| DOID:0060675 | catecholaminergic polymorphic ventricular tachycardia 1 | HGNC:10484 | Homo sapiens (human) | 6262 | RYR2 |
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| DOID:0050956 | spinocerebellar ataxia type 6 | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:0080097 | myofibrillar myopathy 6 | HGNC:939 | Homo sapiens (human) | 9531 | BAG3 |
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| DOID:0060703 | Muenke Syndrome | HGNC:3690 | Homo sapiens (human) | 2261 | FGFR3 |
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| DOID:0111735 | X-linked deafness 4 | HGNC:11122 | Homo sapiens (human) | 23676 | SMPX |
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| DOID:0110640 | congenital muscular dystrophy due to LMNA mutation | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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| DOID:0110431 | dilated cardiomyopathy 1I | HGNC:2770 | Homo sapiens (human) | 1674 | DES |
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| DOID:0111013 | cone-rod dystrophy 3 | HGNC:34 | Homo sapiens (human) | 24 | ABCA4 |
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| DOID:9256 | colorectal cancer | HGNC:583 | Homo sapiens (human) | 324 | APC |
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| DOID:0111272 | occipital horn syndrome | HGNC:869 | Homo sapiens (human) | 538 | ATP7A |
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