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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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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:0111240 | congenital muscular dystrophy-dystroglycanopathy type A2 | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0112184 | thyroid dyshormonogenesis 5 | HGNC:32698 | Homo sapiens (human) | 405753 | DUOXA2 |
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| DOID:0111524 | autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 5 | HGNC:11992 | Homo sapiens (human) | 7156 | TOP3A |
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| DOID:10123 | pigmentation disease | HGNC:4868 | Homo sapiens (human) | 8924 | HERC2 |
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| DOID:0060746 | basal laminar drusen | HGNC:4883 | Homo sapiens (human) | 3075 | CFH |
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| DOID:612 | primary immunodeficiency disease | HGNC:29002 | Homo sapiens (human) | 23149 | FCHO1 |
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| DOID:13099 | Moyamoya disease | HGNC:14539 | Homo sapiens (human) | 57674 | RNF213 |
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| DOID:0110479 | autosomal recessive nonsyndromic deafness 21 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:0070400 | hypomyelinating leukodystrophy 19 | HGNC:29118 | Homo sapiens (human) | 9725 | TMEM63A |
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| DOID:0110980 | Joubert syndrome 1 | HGNC:21474 | Homo sapiens (human) | 56623 | INPP5E |
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| DOID:0070050 | neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language | HGNC:6996 | Homo sapiens (human) | 4208 | MEF2C |
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| DOID:0081150 | common variable immunodeficiency 7 | HGNC:2336 | Homo sapiens (human) | 1380 | CR2 |
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| DOID:0111843 | Paganini-Miozzo syndrome | HGNC:19133 | Homo sapiens (human) | 90161 | HS6ST2 |
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| DOID:0070035 | autosomal dominant intellectual developmental disorder 5 | HGNC:11497 | Homo sapiens (human) | 8831 | SYNGAP1 |
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| DOID:0070411 | autosomal recessive spinocerebellar ataxia 30 | HGNC:17663 | Homo sapiens (human) | 10531 | PITRM1 |
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| DOID:0112233 | lissencephaly 8 | HGNC:26899 | Homo sapiens (human) | 160418 | TMTC3 |
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| DOID:1612 | breast cancer | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:0110241 | cataract 41 | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:0110751 | type 1 diabetes mellitus 12 | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:0111296 | generalized epilepsy with febrile seizures plus 10 | HGNC:4845 | Homo sapiens (human) | 348980 | HCN1 |
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| DOID:0081113 | Baraitser-Winter syndrome 2 | HGNC:144 | Homo sapiens (human) | 71 | ACTG1 |
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| DOID:12849 | autistic disorder | HGNC:20653 | Homo sapiens (human) | 285195 | SLC9A9 |
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| DOID:11252 | microcytic anemia | HGNC:16517 | Homo sapiens (human) | 164656 | TMPRSS6 |
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| DOID:9256 | colorectal cancer | HGNC:959 | Homo sapiens (human) | 581 | BAX |
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| DOID:10123 | pigmentation disease | HGNC:12442 | Homo sapiens (human) | 7299 | TYR |
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