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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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MIRAGE
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:4441 | dysgerminoma | HGNC:6065 | Homo sapiens (human) | 3623 | INHA |
|
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| DOID:2997 | Sertoli-Leydig cell tumor | HGNC:6065 | Homo sapiens (human) | 3623 | INHA |
|
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| DOID:10286 | prostate carcinoma | HGNC:6065 | Homo sapiens (human) | 3623 | INHA |
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| DOID:10283 | prostate cancer | HGNC:6065 | Homo sapiens (human) | 3623 | INHA |
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| DOID:2696 | Leydig cell tumor | HGNC:6065 | Homo sapiens (human) | 3623 | INHA |
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| DOID:3308 | embryonal carcinoma | HGNC:6065 | Homo sapiens (human) | 3623 | INHA |
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| DOID:4440 | seminoma | HGNC:6065 | Homo sapiens (human) | 3623 | INHA |
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| DOID:0050661 | vitelliform macular dystrophy | HGNC:6055 | Homo sapiens (human) | 3617 | IMPG1 |
|
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| DOID:10584 | retinitis pigmentosa | HGNC:6055 | Homo sapiens (human) | 3617 | IMPG1 |
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| DOID:3312 | bipolar disorder | HGNC:6051 | Homo sapiens (human) | 3613 | IMPA2 |
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| DOID:5419 | schizophrenia | HGNC:6051 | Homo sapiens (human) | 3613 | IMPA2 |
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| DOID:0081221 | autosomal recessive intellectual developmental disorder 59 | HGNC:6050 | Homo sapiens (human) | 3612 | IMPA1 |
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| DOID:1059 | intellectual disability | HGNC:6050 | Homo sapiens (human) | 3612 | IMPA1 |
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| DOID:0050169 | cutaneous lupus erythematosus | HGNC:5981 | Homo sapiens (human) | 3605 | IL17A |
|
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| DOID:4481 | allergic rhinitis | HGNC:5981 | Homo sapiens (human) | 3605 | IL17A |
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| DOID:9074 | systemic lupus erythematosus | HGNC:5981 | Homo sapiens (human) | 3605 | IL17A |
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| DOID:3770 | pulmonary fibrosis | HGNC:5981 | Homo sapiens (human) | 3605 | IL17A |
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| DOID:823 | periapical periodontitis | HGNC:5981 | Homo sapiens (human) | 3605 | IL17A |
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| DOID:8893 | psoriasis | HGNC:5981 | Homo sapiens (human) | 3605 | IL17A |
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| DOID:9008 | psoriatic arthritis | HGNC:5981 | Homo sapiens (human) | 3605 | IL17A |
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| DOID:1273 | respiratory syncytial virus infectious disease | HGNC:5981 | Homo sapiens (human) | 3605 | IL17A |
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| DOID:2755 | Mycobacterium avium complex disease | HGNC:5981 | Homo sapiens (human) | 3605 | IL17A |
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| DOID:13141 | uveitis | HGNC:5981 | Homo sapiens (human) | 3605 | IL17A |
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| DOID:2841 | asthma | HGNC:5981 | Homo sapiens (human) | 3605 | IL17A |
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| DOID:1024 | leprosy | HGNC:5981 | Homo sapiens (human) | 3605 | IL17A |
|
