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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:0060019 | coronin-1A deficiency | HGNC:2252 | Homo sapiens (human) | 11151 | CORO1A |
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| DOID:0110290 | autosomal recessive limb-girdle muscular dystrophy type 2X | HGNC:1152 | Homo sapiens (human) | 11149 | POPDC1 |
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| DOID:6419 | tetralogy of Fallot | HGNC:1152 | Homo sapiens (human) | 11149 | POPDC1 |
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| DOID:0110290 | autosomal recessive limb-girdle muscular dystrophy type 2X | HGNC:1152 | Homo sapiens (human) | 11149 | BVES |
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| DOID:6419 | tetralogy of Fallot | HGNC:1152 | Homo sapiens (human) | 11149 | BVES |
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| DOID:2436 | glomangioma | HGNC:14373 | Homo sapiens (human) | 11146 | GLMN |
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| DOID:11294 | arteriovenous malformation | HGNC:14373 | Homo sapiens (human) | 11146 | GLMN |
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| DOID:2431 | glomus tumor | HGNC:14373 | Homo sapiens (human) | 11146 | GLMN |
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| DOID:4440 | seminoma | HGNC:17825 | Homo sapiens (human) | 11145 | PLAAT3 |
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| DOID:4674 | androgen insensitivity syndrome | HGNC:17016 | Homo sapiens (human) | 11143 | KAT7 |
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| DOID:1612 | breast cancer | HGNC:17016 | Homo sapiens (human) | 11143 | KAT7 |
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| DOID:1059 | intellectual disability | HGNC:5996 | Homo sapiens (human) | 11141 | IL1RAPL1 |
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| DOID:0112022 | non-syndromic X-linked intellectual disability 21 | HGNC:5996 | Homo sapiens (human) | 11141 | IL1RAPL1 |
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| DOID:11612 | polycystic ovary syndrome | HGNC:1477 | Homo sapiens (human) | 11132 | CAPN10 |
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| DOID:1793 | pancreatic cancer | HGNC:1477 | Homo sapiens (human) | 11132 | CAPN10 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1477 | Homo sapiens (human) | 11132 | CAPN10 |
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| DOID:9970 | obesity | HGNC:1477 | Homo sapiens (human) | 11132 | CAPN10 |
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| DOID:10763 | hypertension | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:2986 | IgA glomerulonephritis | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:783 | end stage renal disease | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:10283 | prostate cancer | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:0050771 | pheochromocytoma | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:0081333 | Wiedemann-Rautenstrauch syndrome | HGNC:30074 | Homo sapiens (human) | 11128 | POLR3A |
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| DOID:0060786 | hypomyelinating leukodystrophy | HGNC:30074 | Homo sapiens (human) | 11128 | POLR3A |
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| DOID:0060794 | hypomyelinating leukodystrophy 7 | HGNC:30074 | Homo sapiens (human) | 11128 | POLR3A |
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