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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:0110617 | primary ciliary dyskinesia 5 | HGNC:19368 | Homo sapiens (human) | 54768 | HYDIN |
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| DOID:1380 | endometrial cancer | HGNC:7329 | Homo sapiens (human) | 2956 | MSH6 |
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| DOID:0110032 | autosomal dominant Alport syndrome | HGNC:2204 | Homo sapiens (human) | 1285 | COL4A3 |
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| DOID:0112202 | developmental and epileptic encephalopathy | HGNC:20566 | Homo sapiens (human) | 9900 | SV2A |
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| DOID:0081217 | autosomal recessive intellectual developmental disorder 56 | HGNC:20509 | Homo sapiens (human) | 79882 | ZC3H14 |
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| DOID:10908 | hydrocephalus | HGNC:19967 | Homo sapiens (human) | 440193 | CCDC88C |
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| DOID:0070070 | autosomal dominant intellectual developmental disorder 40 | HGNC:20311 | Homo sapiens (human) | 283489 | CHAMP1 |
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| DOID:0080071 | mucolipidosis III alpha/beta | HGNC:29670 | Homo sapiens (human) | 79158 | GNPTAB |
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| DOID:0080584 | autosomal dominant Wolfram syndrome | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:0060174 | GABA aminotransferase deficiency | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:0112250 | Gaucher's disease type IIIC | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0111465 | combined oxidative phosphorylation deficiency 21 | HGNC:30740 | Homo sapiens (human) | 80222 | TARS2 |
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| DOID:0110595 | Stromme syndrome | HGNC:1857 | Homo sapiens (human) | 1063 | CENPF |
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| DOID:0111677 | familial benign fleck retina | HGNC:9038 | Homo sapiens (human) | 5322 | PLA2G5 |
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| DOID:0080626 | corticosterone methyloxidase deficiency 1 | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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| DOID:0112310 | central precocious puberty 1 | HGNC:4510 | Homo sapiens (human) | 84634 | KISS1R |
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| DOID:0080411 | familial adenomatous polyposis 3 | HGNC:8028 | Homo sapiens (human) | 4913 | NTHL1 |
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| DOID:0110031 | hemoglobin H disease | HGNC:4824 | Homo sapiens (human) | 3040 | HBA2 |
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| DOID:0110294 | autosomal recessive limb-girdle muscular dystrophy type 2T | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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| DOID:14764 | Larsen syndrome | HGNC:3755 | Homo sapiens (human) | 2317 | FLNB |
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| DOID:0111667 | enterokinase deficiency | HGNC:9490 | Homo sapiens (human) | 5651 | TMPRSS15 |
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| DOID:0070219 | familial hyperinsulinemic hypoglycemia 1 | HGNC:59 | Homo sapiens (human) | 6833 | ABCC8 |
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| DOID:0090064 | familial cold autoinflammatory syndrome 3 | HGNC:9066 | Homo sapiens (human) | 5336 | PLCG2 |
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| DOID:0050864 | non-arteritic anterior ischemic optic neuropathy | HGNC:4439 | Homo sapiens (human) | 2811 | GP1BA |
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| DOID:0110273 | autosomal dominant limb-girdle muscular dystrophy | HGNC:1480 | Homo sapiens (human) | 825 | CAPN3 |
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