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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:3070 | high grade glioma | HGNC:18039 | Homo sapiens (human) | 10765 | KDM5B |
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| DOID:1612 | breast cancer | HGNC:18039 | Homo sapiens (human) | 10765 | KDM5B |
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| DOID:11054 | urinary bladder cancer | HGNC:18039 | Homo sapiens (human) | 10765 | KDM5B |
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| DOID:10283 | prostate cancer | HGNC:18039 | Homo sapiens (human) | 10765 | KDM5B |
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| DOID:1574 | alcohol use disorder | HGNC:18039 | Homo sapiens (human) | 10765 | KDM5B |
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| DOID:0060041 | autism spectrum disorder | HGNC:18039 | Homo sapiens (human) | 10765 | KDM5B |
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| DOID:0050888 | syndromic intellectual disability | HGNC:18039 | Homo sapiens (human) | 10765 | KDM5B |
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| DOID:0060809 | syndromic X-linked intellectual disability Claes-Jensen type | HGNC:18039 | Homo sapiens (human) | 10765 | KDM5B |
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| DOID:6039 | uveal melanoma | HGNC:18039 | Homo sapiens (human) | 10765 | KDM5B |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:18039 | Homo sapiens (human) | 10765 | KDM5B |
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| DOID:0081226 | autosomal recessive intellectual developmental disorder 65 | HGNC:18039 | Homo sapiens (human) | 10765 | KDM5B |
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| DOID:2527 | nephrosis | HGNC:7756 | Homo sapiens (human) | 10763 | NES |
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| DOID:2316 | brain ischemia | HGNC:7756 | Homo sapiens (human) | 10763 | NES |
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| DOID:3454 | brain infarction | HGNC:7756 | Homo sapiens (human) | 10763 | NES |
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| DOID:3021 | acute kidney failure | HGNC:7756 | Homo sapiens (human) | 10763 | NES |
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| DOID:1289 | neurodegenerative disease | HGNC:8065 | Homo sapiens (human) | 10762 | NUP50 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:1343 | Homo sapiens (human) | 10758 | TRAF3IP2 |
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| DOID:3310 | atopic dermatitis | HGNC:1343 | Homo sapiens (human) | 10758 | TRAF3IP2 |
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| DOID:2058 | chronic mucocutaneous candidiasis | HGNC:1343 | Homo sapiens (human) | 10758 | TRAF3IP2 |
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| DOID:0111287 | psoriasis 13 | HGNC:1343 | Homo sapiens (human) | 10758 | TRAF3IP2 |
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| DOID:12894 | Sjogren's syndrome | HGNC:1343 | Homo sapiens (human) | 10758 | TRAF3IP2 |
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| DOID:1826 | epilepsy | HGNC:1939 | Homo sapiens (human) | 10752 | CHL1 |
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| DOID:5419 | schizophrenia | HGNC:1939 | Homo sapiens (human) | 10752 | CHL1 |
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| DOID:0060246 | MASA syndrome | HGNC:1939 | Homo sapiens (human) | 10752 | CHL1 |
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| DOID:1686 | glaucoma | MGI:1891468 | Mus musculus (house mouse) | 107515 | Lgr4 |
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