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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:0110984 | Joubert syndrome 15 | HGNC:12370 | Homo sapiens (human) | 95681 | CEP41 |
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| DOID:0110031 | hemoglobin H disease | HGNC:4823 | Homo sapiens (human) | 3039 | HBA1 |
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| DOID:0112168 | autosomal dominant nonsyndromic deafness 77 | HGNC:51 | Homo sapiens (human) | 4363 | ABCC1 |
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| DOID:0112215 | developmental and epileptic encephalopathy 79 | HGNC:4079 | Homo sapiens (human) | 2558 | GABRA5 |
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| DOID:14681 | Silver-Russell syndrome | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:0112186 | thyroid dyshormonogenesis 2A | HGNC:12015 | Homo sapiens (human) | 7173 | TPO |
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| DOID:0050648 | atelosteogenesis | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:0111188 | myofibrillar myopathy 9 | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
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| DOID:11719 | oculopharyngeal muscular dystrophy | HGNC:8565 | Homo sapiens (human) | 8106 | PABPN1 |
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| DOID:0080319 | X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia | HGNC:28880 | Homo sapiens (human) | 84061 | MAGT1 |
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| DOID:0060576 | 3MC syndrome 2 | HGNC:17213 | Homo sapiens (human) | 78989 | COLEC11 |
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| DOID:0080634 | nanophthalmos | HGNC:18121 | Homo sapiens (human) | 83552 | MFRP |
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| DOID:0050648 | atelosteogenesis | HGNC:3755 | Homo sapiens (human) | 2317 | FLNB |
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| DOID:0111530 | linear nevus sebaceous syndrome | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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| DOID:0110736 | neurodegeneration with brain iron accumulation 2b | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:0110220 | Brugada syndrome 3 | HGNC:1390 | Homo sapiens (human) | 775 | CACNA1C |
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| DOID:0112373 | autosomal dominant auditory neuropathy 3 | HGNC:28472 | Homo sapiens (human) | 79188 | TMEM43 |
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| DOID:0080453 | developmental and epileptic encephalopathy 25 | HGNC:23089 | Homo sapiens (human) | 284111 | SLC13A5 |
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| DOID:0080118 | mitochondrial complex III deficiency nuclear type 9 | HGNC:34399 | Homo sapiens (human) | 790955 | UQCC3 |
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| DOID:0111935 | immunodeficiency 16 | HGNC:11918 | Homo sapiens (human) | 7293 | TNFRSF4 |
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| DOID:0111406 | Fraser syndrome 3 | HGNC:18708 | Homo sapiens (human) | 23426 | GRIP1 |
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| DOID:2907 | Goldenhar syndrome | HGNC:10769 | Homo sapiens (human) | 10992 | SF3B2 |
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| DOID:0111461 | cardiofaciocutaneous syndrome 2 | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:4571 | Homo sapiens (human) | 2890 | GRIA1 |
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| DOID:0070221 | progressive familial intrahepatic cholestasis | HGNC:10741 | Homo sapiens (human) | 8482 | SEMA7A |
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