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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:14761 | Greig cephalopolysyndactyly syndrome | HGNC:4319 | Homo sapiens (human) | 2737 | GLI3 |
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| DOID:10763 | hypertension | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:784 | chronic kidney disease | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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| DOID:0060445 | congenital stromal corneal dystrophy | HGNC:2705 | Homo sapiens (human) | 1634 | DCN |
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| DOID:8584 | Burkitt lymphoma | HGNC:7553 | Homo sapiens (human) | 4609 | MYC |
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| DOID:1596 | depressive disorder | HGNC:2356 | Homo sapiens (human) | 1393 | CRHBP |
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| DOID:2030 | anxiety disorder | HGNC:11050 | Homo sapiens (human) | 6532 | SLC6A4 |
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| DOID:0070005 | Seckel syndrome 9 | HGNC:30764 | Homo sapiens (human) | 10293 | TRAIP |
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| DOID:0111330 | combined saposin deficiency | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:0110826 | Usher syndrome type 1 | HGNC:7606 | Homo sapiens (human) | 4647 | MYO7A |
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| DOID:0110847 | xeroderma pigmentosum variant type | HGNC:9181 | Homo sapiens (human) | 5429 | POLH |
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| DOID:0060696 | hyperekplexia 1 | HGNC:4326 | Homo sapiens (human) | 2741 | GLRA1 |
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| DOID:0111742 | cerebellar ataxia type 42 | HGNC:1394 | Homo sapiens (human) | 8913 | CACNA1G |
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| DOID:0050797 | peroxisomal acyl-CoA oxidase deficiency | HGNC:119 | Homo sapiens (human) | 51 | ACOX1 |
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| DOID:0050579 | glycogen storage disease XV | HGNC:4699 | Homo sapiens (human) | 2992 | GYG1 |
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| DOID:0060776 | congenital diarrhea 5 with tufting enteropathy | HGNC:11529 | Homo sapiens (human) | 4072 | EPCAM |
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| DOID:0110151 | Charcot-Marie-Tooth disease type 1C | HGNC:16841 | Homo sapiens (human) | 9516 | LITAF |
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| DOID:0060540 | Hermansky-Pudlak syndrome 2 | HGNC:566 | Homo sapiens (human) | 8546 | AP3B1 |
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| DOID:0112245 | focal segmental glomerulosclerosis 3 | HGNC:14258 | Homo sapiens (human) | 23607 | CD2AP |
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| DOID:0050958 | spinocerebellar ataxia type 7 | HGNC:10560 | Homo sapiens (human) | 6314 | ATXN7 |
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| DOID:446 | primary hyperaldosteronism | HGNC:2020 | Homo sapiens (human) | 1181 | CLCN2 |
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| DOID:0111700 | ankyrin-B-related cardiac arrhythmia | HGNC:493 | Homo sapiens (human) | 287 | ANK2 |
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| DOID:14365 | systemic primary carnitine deficiency disease | HGNC:10969 | Homo sapiens (human) | 6584 | SLC22A5 |
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| DOID:0060601 | alpha-2-plasmin inhibitor deficiency | HGNC:9075 | Homo sapiens (human) | 5345 | SERPINF2 |
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| DOID:0090074 | hypogonadotropic hypogonadism 8 with or without anosmia | HGNC:4510 | Homo sapiens (human) | 84634 | KISS1R |
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