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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
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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▼ | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:33882 | Homo sapiens (human) | 51763 | INPP5K |
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| DOID:0080197 | congenital muscular dystrophy with cataracts and intellectual disability | HGNC:33882 | Homo sapiens (human) | 51763 | INPP5K |
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| DOID:0110980 | Joubert syndrome 1 | FB:FBgn0036273 | Drosophila melanogaster (fruit fly) | 39404 | INPP5E |
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| DOID:0050777 | Joubert syndrome | HGNC:21474 | Homo sapiens (human) | 56623 | INPP5E |
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| DOID:0050777 | Joubert syndrome | FB:FBgn0036273 | Drosophila melanogaster (fruit fly) | 39404 | INPP5E |
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| DOID:9970 | obesity | FB:FBgn0036273 | Drosophila melanogaster (fruit fly) | 39404 | INPP5E |
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| DOID:0110980 | Joubert syndrome 1 | HGNC:21474 | Homo sapiens (human) | 56623 | INPP5E |
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| DOID:9970 | obesity | HGNC:21474 | Homo sapiens (human) | 56623 | INPP5E |
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| DOID:5408 | Paget's disease of bone | HGNC:6079 | Homo sapiens (human) | 3635 | INPP5D |
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| DOID:9074 | systemic lupus erythematosus | HGNC:6079 | Homo sapiens (human) | 3635 | INPP5D |
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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:1059 | intellectual disability | HGNC:6050 | Homo sapiens (human) | 3612 | IMPA1 |
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| DOID:0081221 | autosomal recessive intellectual developmental disorder 59 | HGNC:6050 | Homo sapiens (human) | 3612 | IMPA1 |
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| DOID:9266 | cystinuria | SGD:S000003752 | Saccharomyces cerevisiae S288C | 853214 | IMA5 |
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| DOID:9266 | cystinuria | SGD:S000003757 | Saccharomyces cerevisiae S288C | 853235 | IMA4 |
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| DOID:9266 | cystinuria | SGD:S000001434 | Saccharomyces cerevisiae S288C | 854635 | IMA3 |
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| DOID:9266 | cystinuria | SGD:S000005517 | Saccharomyces cerevisiae S288C | 854008 | IMA2 |
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| DOID:9266 | cystinuria | SGD:S000003519 | Saccharomyces cerevisiae S288C | 853204 | IMA1 |
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| DOID:11832 | visual epilepsy | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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| DOID:0080596 | hyper IgE recurrent infection syndrome 4 | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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| DOID:10652 | Alzheimer's disease | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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| DOID:10763 | hypertension | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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| DOID:7148 | rheumatoid arthritis | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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| DOID:612 | primary immunodeficiency disease | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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