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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:0090026 | split hand-foot malformation 6 | HGNC:12775 | Homo sapiens (human) | 7480 | WNT10B |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:6893 | Homo sapiens (human) | 4137 | MAPT |
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| DOID:612 | primary immunodeficiency disease | HGNC:708 | Homo sapiens (human) | 10092 | ARPC5 |
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| DOID:0111646 | congenital lactase deficiency | HGNC:6530 | Homo sapiens (human) | 3938 | LCT |
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| DOID:2043 | hepatitis B | HGNC:19191 | Homo sapiens (human) | 81704 | DOCK8 |
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| DOID:0112182 | mismatch repair cancer syndrome | HGNC:7127 | Homo sapiens (human) | 4292 | MLH1 |
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| DOID:0060263 | porencephaly | HGNC:2203 | Homo sapiens (human) | 1284 | COL4A2 |
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| DOID:2378 | relapsing-remitting multiple sclerosis | HGNC:11920 | Homo sapiens (human) | 355 | FAS |
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| DOID:10591 | pre-eclampsia | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:2841 | asthma | HGNC:1950 | Homo sapiens (human) | 1128 | CHRM1 |
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| DOID:9256 | colorectal cancer | HGNC:11386 | Homo sapiens (human) | 6786 | STIM1 |
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| DOID:1214 | tympanosclerosis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:1883 | hepatitis C | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:1852 | intrahepatic cholestasis | HGNC:42 | Homo sapiens (human) | 8647 | ABCB11 |
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| DOID:0050748 | marginal zone lymphoma | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0080205 | CAKUT | HGNC:8001 | Homo sapiens (human) | 8204 | NRIP1 |
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| DOID:0050741 | alcohol dependence | HGNC:2303 | Homo sapiens (human) | 1363 | CPE |
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| DOID:4927 | Klatskin's tumor | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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| DOID:0110680 | congenital myasthenic syndrome 2C | HGNC:1961 | Homo sapiens (human) | 1140 | CHRNB1 |
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| DOID:83 | cataract | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:0050776 | non-syndromic X-linked intellectual disability | HGNC:13054 | Homo sapiens (human) | 9203 | ZMYM3 |
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| DOID:1682 | congenital heart disease | HGNC:17075 | Homo sapiens (human) | 23118 | TAB2 |
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| DOID:5844 | myocardial infarction | HGNC:6623 | Homo sapiens (human) | 9388 | LIPG |
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| DOID:11476 | osteoporosis | HGNC:11180 | Homo sapiens (human) | 6648 | SOD2 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:11773 | Homo sapiens (human) | 7048 | TGFBR2 |
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