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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:9074 | systemic lupus erythematosus | MGI:2144765 | Mus musculus (house mouse) | 104759 | Pld4 |
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| DOID:8161 | thyroid gland Hurthle cell carcinoma | HGNC:17316 | Homo sapiens (human) | 10469 | TIMM44 |
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| DOID:8947 | diabetic retinopathy | HGNC:17316 | Homo sapiens (human) | 10469 | TIMM44 |
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| DOID:13207 | proliferative diabetic retinopathy | HGNC:17316 | Homo sapiens (human) | 10469 | TIMM44 |
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| DOID:0060762 | restrictive dermopathy | HGNC:3971 | Homo sapiens (human) | 10468 | FST |
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| DOID:11612 | polycystic ovary syndrome | HGNC:3971 | Homo sapiens (human) | 10468 | FST |
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| DOID:0070261 | congenital disorder of glycosylation type IIi | HGNC:14857 | Homo sapiens (human) | 10466 | COG5 |
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| DOID:0110367 | retinitis pigmentosa 38 | HGNC:7027 | Homo sapiens (human) | 10461 | MERTK |
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| DOID:8466 | retinal degeneration | HGNC:7027 | Homo sapiens (human) | 10461 | MERTK |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:947 | Homo sapiens (human) | 10458 | BAIAP2 |
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| DOID:10652 | Alzheimer's disease | HGNC:947 | Homo sapiens (human) | 10458 | BAIAP2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:947 | Homo sapiens (human) | 10458 | BAIAP2 |
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| DOID:11119 | Gilles de la Tourette syndrome | HGNC:947 | Homo sapiens (human) | 10458 | BAIAP2 |
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| DOID:0060680 | pigment dispersion syndrome | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
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| DOID:0080932 | primary localized cutaneous amyloidosis 3 | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
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| DOID:3454 | brain infarction | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
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| DOID:0050590 | severe congenital neutropenia | HGNC:16915 | Homo sapiens (human) | 10456 | HAX1 |
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| DOID:0112133 | severe congenital neutropenia 3 | HGNC:16915 | Homo sapiens (human) | 10456 | HAX1 |
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| DOID:3526 | cerebral infarction | HGNC:18001 | Homo sapiens (human) | 10452 | TOMM40 |
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| DOID:10652 | Alzheimer's disease | HGNC:18001 | Homo sapiens (human) | 10452 | TOMM40 |
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| DOID:0060791 | hypomyelinating leukodystrophy 9 | MGI:1914297 | Mus musculus (house mouse) | 104458 | Rars1 |
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| DOID:0050908 | myelodysplastic syndrome | MGI:1206586 | Mus musculus (house mouse) | 104416 | Bap1 |
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| DOID:4928 | intrahepatic cholangiocarcinoma | MGI:1206586 | Mus musculus (house mouse) | 104416 | Bap1 |
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| DOID:6039 | uveal melanoma | MGI:1206586 | Mus musculus (house mouse) | 104416 | Bap1 |
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| DOID:3495 | extrahepatic bile duct adenocarcinoma | MGI:1206586 | Mus musculus (house mouse) | 104416 | Bap1 |
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