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GlyTouCan
Glycan Structure Repository
GlyComb
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:9884 | muscular dystrophy | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0081297 | oculopharyngodistal myopathy 1 | HGNC:31708 | Homo sapiens (human) | 29967 | LRP12 |
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| DOID:10003 | sensorineural hearing loss | HGNC:16361 | Homo sapiens (human) | 25861 | WHRN |
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| DOID:4483 | rhinitis | HGNC:6015 | Homo sapiens (human) | 3566 | IL4R |
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| DOID:4448 | macular degeneration | HGNC:6307 | Homo sapiens (human) | 3791 | KDR |
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| DOID:10591 | pre-eclampsia | HGNC:4931 | Homo sapiens (human) | 3105 | HLA-A |
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| DOID:936 | brain disease | HGNC:24858 | Homo sapiens (human) | 56947 | MFF |
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| DOID:0111681 | glutamate-cysteine ligase deficiency | HGNC:4311 | Homo sapiens (human) | 2729 | GCLC |
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| DOID:0080289 | orofaciodigital syndrome XVII | HGNC:29239 | Homo sapiens (human) | 27152 | INTU |
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| DOID:2018 | hyperinsulinism | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:0060060 | non-Hodgkin lymphoma | HGNC:9360 | Homo sapiens (human) | 5551 | PRF1 |
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| DOID:3774 | chordoid glioma | HGNC:9393 | Homo sapiens (human) | 5578 | PRKCA |
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| DOID:0111866 | trichothiodystrophy | HGNC:6898 | Homo sapiens (human) | 4141 | MARS1 |
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| DOID:0060643 | primary sclerosing cholangitis | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:0060058 | lymphoma | HGNC:8575 | Homo sapiens (human) | 5049 | PAFAH1B2 |
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| DOID:12361 | Graves' disease | HGNC:2976 | Homo sapiens (human) | 1786 | DNMT1 |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:0111644 | autosomal recessive nonsyndromic deafness 110 | HGNC:2180 | Homo sapiens (human) | 1690 | COCH |
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| DOID:3393 | coronary artery disease | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:0081202 | autosomal recessive intellectual developmental disorder 37 | HGNC:494 | Homo sapiens (human) | 288 | ANK3 |
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| DOID:612 | primary immunodeficiency disease | HGNC:9666 | Homo sapiens (human) | 5788 | PTPRC |
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| DOID:11257 | social phobia | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:2043 | hepatitis B | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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| DOID:0081190 | autosomal recessive intellectual developmental disorder 18 | HGNC:2372 | Homo sapiens (human) | 9439 | MED23 |
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| DOID:0080600 | COVID-19 | HGNC:6340 | Homo sapiens (human) | 3813 | KIR3DS1 |
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