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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:2671 | transitional cell carcinoma | HGNC:4510 | Homo sapiens (human) | 84634 | KISS1R |
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| DOID:1924 | hypogonadism | HGNC:4510 | Homo sapiens (human) | 84634 | KISS1R |
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| DOID:3113 | papillary carcinoma | HGNC:4510 | Homo sapiens (human) | 84634 | KISS1R |
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| DOID:0112310 | central precocious puberty 1 | HGNC:4510 | Homo sapiens (human) | 84634 | KISS1R |
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| DOID:1612 | breast cancer | HGNC:4510 | Homo sapiens (human) | 84634 | KISS1R |
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| DOID:0090074 | hypogonadotropic hypogonadism 8 with or without anosmia | HGNC:4510 | Homo sapiens (human) | 84634 | KISS1R |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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| DOID:784 | chronic kidney disease | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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| DOID:9452 | steatotic liver disease | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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| DOID:0060793 | hypomyelinating leukodystrophy 5 | MGI:2149839 | Mus musculus (house mouse) | 84652 | Hycc1 |
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| DOID:0110933 | nemaline myopathy 11 | HGNC:23246 | Homo sapiens (human) | 84665 | MYPN |
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| DOID:0110445 | dilated cardiomyopathy 1KK | HGNC:23246 | Homo sapiens (human) | 84665 | MYPN |
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| DOID:397 | restrictive cardiomyopathy | HGNC:23246 | Homo sapiens (human) | 84665 | MYPN |
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| DOID:0060793 | hypomyelinating leukodystrophy 5 | HGNC:24587 | Homo sapiens (human) | 84668 | HYCC1 |
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| DOID:331 | central nervous system disease | HGNC:11101 | Homo sapiens (human) | 8467 | SMARCA5 |
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| DOID:767 | muscular atrophy | HGNC:16007 | Homo sapiens (human) | 84676 | TRIM63 |
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| DOID:14557 | primary pulmonary hypertension | HGNC:16007 | Homo sapiens (human) | 84676 | TRIM63 |
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| DOID:9884 | muscular dystrophy | HGNC:16007 | Homo sapiens (human) | 84676 | TRIM63 |
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| DOID:3587 | pancreatic ductal carcinoma | HGNC:13610 | Homo sapiens (human) | 84678 | KDM2B |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:13610 | Homo sapiens (human) | 84678 | KDM2B |
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| DOID:0081312 | T-cell non-Hodgkin lymphoma | HGNC:13610 | Homo sapiens (human) | 84678 | KDM2B |
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| DOID:0111844 | X-linked intellectual developmental disorder 108 | HGNC:17123 | Homo sapiens (human) | 84679 | SLC9A7 |
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| DOID:5419 | schizophrenia | HGNC:9298 | Homo sapiens (human) | 84687 | PPP1R9B |
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| DOID:684 | hepatocellular carcinoma | HGNC:9298 | Homo sapiens (human) | 84687 | PPP1R9B |
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| DOID:14330 | Parkinson's disease | HGNC:9298 | Homo sapiens (human) | 84687 | PPP1R9B |
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