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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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MIRAGE
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:0060468 | Holt-Oram syndrome | HGNC:15924 | Homo sapiens (human) | 57167 | SALL4 |
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| DOID:0080455 | developmental and epileptic encephalopathy 52 | HGNC:10586 | Homo sapiens (human) | 6324 | SCN1B |
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| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:1331 | Homo sapiens (human) | 727 | C5 |
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| DOID:0080162 | lupus nephritis | HGNC:6149 | Homo sapiens (human) | 3684 | ITGAM |
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| DOID:0080244 | Galloway-Mowat syndrome 2 | HGNC:26058 | Homo sapiens (human) | 8270 | LAGE3 |
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| DOID:5844 | myocardial infarction | HGNC:2202 | Homo sapiens (human) | 1282 | COL4A1 |
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| DOID:9182 | pemphigus | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:0060536 | mitochondrial complex I deficiency | HGNC:7707 | Homo sapiens (human) | 4719 | NDUFS1 |
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| DOID:0112350 | spermatogenic failure 61 | HGNC:11356 | Homo sapiens (human) | 10734 | STAG3 |
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| DOID:0110158 | Charcot-Marie-Tooth disease type 2I | HGNC:7225 | Homo sapiens (human) | 4359 | MPZ |
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| DOID:3526 | cerebral infarction | HGNC:4814 | Homo sapiens (human) | 8997 | KALRN |
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| DOID:10763 | hypertension | RGD:61925 | Rattus norvegicus (Norway rat) | 29340 | Prkce |
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| DOID:8893 | psoriasis | HGNC:1037 | Homo sapiens (human) | 629 | CFB |
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| DOID:1380 | endometrial cancer | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:399 | tuberculosis | HGNC:2615 | Homo sapiens (human) | 1555 | CYP2B6 |
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| DOID:4914 | esophagus adenocarcinoma | HGNC:7155 | Homo sapiens (human) | 4312 | MMP1 |
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| DOID:0060863 | patterned macular dystrophy | HGNC:9942 | Homo sapiens (human) | 5961 | PRPH2 |
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| DOID:0080301 | atypical hemolytic-uremic syndrome | HGNC:16980 | Homo sapiens (human) | 10878 | CFHR3 |
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| DOID:3312 | bipolar disorder | HGNC:10618 | Homo sapiens (human) | 6347 | CCL2 |
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| DOID:0060937 | dystonia 30 | HGNC:14584 | Homo sapiens (human) | 64601 | VPS16 |
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| DOID:1909 | melanoma | HGNC:1101 | Homo sapiens (human) | 675 | BRCA2 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:9206 | Homo sapiens (human) | 5446 | PON3 |
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| DOID:14791 | Leber congenital amaurosis | HGNC:9942 | Homo sapiens (human) | 5961 | PRPH2 |
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| DOID:0111392 | mucopolysaccharidosis type IVB | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:0060774 | congenital diarrhea | HGNC:13635 | Homo sapiens (human) | 83483 | PLVAP |
|
