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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:3908 | lung non-small cell carcinoma | HGNC:13919 | Homo sapiens (human) | 7917 | BAG6 |
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| DOID:11193 | syndactyly | HGNC:4319 | Homo sapiens (human) | 2737 | GLI3 |
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| DOID:0110698 | hypotrichosis 1 | HGNC:11161 | Homo sapiens (human) | 6635 | SNRPE |
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| DOID:13375 | temporal arteritis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0080600 | COVID-19 | HGNC:15631 | Homo sapiens (human) | 51284 | TLR7 |
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| DOID:8778 | Crohn's disease | HGNC:40 | Homo sapiens (human) | 5243 | ABCB1 |
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| DOID:0081421 | familial focal epilepsy with variable foci 1 | HGNC:18423 | Homo sapiens (human) | 9681 | DEPDC5 |
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| DOID:0080484 | peroxisome biogenesis disorder 10A | HGNC:8858 | Homo sapiens (human) | 8504 | PEX3 |
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| DOID:0111907 | thrombophilia due to thrombin defect | HGNC:3535 | Homo sapiens (human) | 2147 | F2 |
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| DOID:0111566 | familial isolated trichomegaly | HGNC:3683 | Homo sapiens (human) | 2250 | FGF5 |
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| DOID:7148 | rheumatoid arthritis | HGNC:11364 | Homo sapiens (human) | 6774 | STAT3 |
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| DOID:0070232 | benign recurrent intrahepatic cholestasis 2 | HGNC:42 | Homo sapiens (human) | 8647 | ABCB11 |
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| DOID:1993 | rectum cancer | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:0080138 | multiple congenital anomalies-hypotonia-seizures syndrome 1 | HGNC:8967 | Homo sapiens (human) | 23556 | PIGN |
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| DOID:12185 | otosclerosis | HGNC:1071 | Homo sapiens (human) | 652 | BMP4 |
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| DOID:4914 | esophagus adenocarcinoma | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:0111743 | cerebellar ataxia type 47 | HGNC:14957 | Homo sapiens (human) | 9698 | PUM1 |
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| DOID:4511 | breast angiosarcoma | HGNC:9665 | Homo sapiens (human) | 5787 | PTPRB |
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| DOID:0080716 | infantile liver failure syndrome | HGNC:21876 | Homo sapiens (human) | 60561 | RINT1 |
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| DOID:12206 | dengue hemorrhagic fever | HGNC:6340 | Homo sapiens (human) | 3813 | KIR3DS1 |
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| DOID:0050700 | cardiomyopathy | HGNC:7871 | Homo sapiens (human) | 4841 | NONO |
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| DOID:0050921 | pharynx squamous cell carcinoma | HGNC:24308 | Homo sapiens (human) | 81037 | CLPTM1L |
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| DOID:1798 | pancreatic endocrine carcinoma | HGNC:7059 | Homo sapiens (human) | 4255 | MGMT |
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| DOID:8893 | psoriasis | HGNC:1037 | Homo sapiens (human) | 629 | CFB |
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| DOID:1205 | allergic disease | HGNC:43 | Homo sapiens (human) | 6890 | TAP1 |
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