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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:289 | endometriosis | HGNC:6972 | Homo sapiens (human) | 4192 | MDK |
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| DOID:0110777 | hereditary spastic paraplegia 26 | RGD:620490 | Rattus norvegicus (Norway rat) | 64828 | B4galnt1 |
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| DOID:3907 | lung squamous cell carcinoma | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:3652 | Leigh disease | HGNC:7461 | Homo sapiens (human) | 4540 | MT-ND5 |
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| DOID:10763 | hypertension | RGD:1308214 | Rattus norvegicus (Norway rat) | 304322 | Chst12 |
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| DOID:0081175 | short stature, hearing loss, retinitis pigmentosa, and distinctive facies | HGNC:17097 | Homo sapiens (human) | 23404 | EXOSC2 |
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| DOID:0060041 | autism spectrum disorder | MGI:1349480 | Mus musculus (house mouse) | 107767 | Scamp1 |
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| DOID:0050437 | Danon disease | MGI:96748 | Mus musculus (house mouse) | 16784 | Lamp2 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:11054 | urinary bladder cancer | HGNC:3432 | Homo sapiens (human) | 2066 | ERBB4 |
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| DOID:2316 | brain ischemia | HGNC:6596 | Homo sapiens (human) | 3976 | LIF |
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| DOID:6000 | congestive heart failure | RGD:2886 | Rattus norvegicus (Norway rat) | 25325 | Il10 |
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| DOID:0110032 | autosomal dominant Alport syndrome | MGI:107717 | Mus musculus (house mouse) | 17886 | Myh9 |
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| DOID:10283 | prostate cancer | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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| DOID:3770 | pulmonary fibrosis | MGI:96547 | Mus musculus (house mouse) | 16181 | Il1rn |
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| DOID:0060844 | Norrie disease | MGI:108520 | Mus musculus (house mouse) | 14366 | Fzd4 |
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| DOID:635 | acquired immunodeficiency syndrome | RGD:727849 | Rattus norvegicus (Norway rat) | 378947 | Bst2 |
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| DOID:5409 | lung small cell carcinoma | HGNC:5021 | Homo sapiens (human) | 3169 | FOXA1 |
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| DOID:8029 | sporadic breast cancer | HGNC:7127 | Homo sapiens (human) | 4292 | MLH1 |
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| DOID:3770 | pulmonary fibrosis | MGI:1346316 | Mus musculus (house mouse) | 24047 | Ccl19 |
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| DOID:4948 | gallbladder carcinoma | Xenbase:XB-GENE-6488967 | Xenopus laevis (African clawed frog) | 108698211 | abo.2.L |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | MGI:99461 | Mus musculus (house mouse) | 18700 | Piga |
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| DOID:0070242 | primary coenzyme Q10 deficiency 5 | MGI:1915164 | Mus musculus (house mouse) | 67914 | Coq9 |
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| DOID:3883 | Lynch syndrome | HGNC:16261 | Homo sapiens (human) | 114571 | SLC22A9 |
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| DOID:1485 | cystic fibrosis | Xenbase:XB-GENE-865765 | Xenopus laevis (African clawed frog) | 397778 | tgfb1.L |
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