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GlyTouCan
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:1935 | Bardet-Biedl syndrome | HGNC:967 | Homo sapiens (human) | 583 | BBS2 |
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| DOID:0111253 | neurofibromatosis 1 | MGI:97306 | Mus musculus (house mouse) | 18015 | Nf1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:11920 | Homo sapiens (human) | 355 | FAS |
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| DOID:14705 | Pfeiffer syndrome | MGI:95523 | Mus musculus (house mouse) | 14183 | Fgfr2 |
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| DOID:12960 | acrocephalosyndactylia | MGI:95523 | Mus musculus (house mouse) | 14183 | Fgfr2 |
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| DOID:6000 | congestive heart failure | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:10325 | silicosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10325 | silicosis | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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| DOID:6432 | pulmonary hypertension | RGD:3714 | Rattus norvegicus (Norway rat) | 25553 | Slc6a4 |
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| DOID:10763 | hypertension | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:2231 | factor XII deficiency | HGNC:3530 | Homo sapiens (human) | 2161 | F12 |
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| DOID:1206 | Rett syndrome | MGI:99918 | Mus musculus (house mouse) | 17257 | Mecp2 |
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| DOID:13636 | Fanconi anemia | HGNC:3585 | Homo sapiens (human) | 2177 | FANCD2 |
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| DOID:3328 | temporal lobe epilepsy | RGD:2735 | Rattus norvegicus (Norway rat) | 24407 | Grik5 |
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| DOID:2842 | Jervell-Lange Nielsen syndrome | MGI:108083 | Mus musculus (house mouse) | 16535 | Kcnq1 |
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| DOID:1206 | Rett syndrome | HGNC:6990 | Homo sapiens (human) | 4204 | MECP2 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:5993 | Homo sapiens (human) | 3554 | IL1R1 |
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| DOID:9970 | obesity | HGNC:7842 | Homo sapiens (human) | 4828 | NMB |
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| DOID:12120 | pulmonary alveolar proteinosis | HGNC:2434 | Homo sapiens (human) | 1437 | CSF2 |
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| DOID:10584 | retinitis pigmentosa | HGNC:10024 | Homo sapiens (human) | 6017 | RLBP1 |
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| DOID:4154 | dentinogenesis imperfecta | HGNC:3054 | Homo sapiens (human) | 1834 | DSPP |
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| DOID:14778 | blepharophimosis, ptosis, and epicanthus inversus syndrome | HGNC:1092 | Homo sapiens (human) | 668 | FOXL2 |
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| DOID:12802 | mucopolysaccharidosis I | HGNC:5391 | Homo sapiens (human) | 3425 | IDUA |
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| DOID:0110671 | congenital myasthenic syndrome 6 | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:1094 | attention deficit hyperactivity disorder | MGI:94862 | Mus musculus (house mouse) | 13162 | Slc6a3 |
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