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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:0050777 | Joubert syndrome | HGNC:21474 | Homo sapiens (human) | 56623 | 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:3211 | lysosomal storage disease | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:9455 | lipid storage disease | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:0110961 | atypical Gaucher's disease due to saposin c deficiency | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:10587 | Krabbe disease | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:0111330 | combined saposin deficiency | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:10581 | metachromatic leukodystrophy | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:0112315 | brain small vessel disease 3 | ZFIN:ZDB-GENE-070720-6 | Danio rerio (zebrafish) | 565862 | colgalt1a |
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| DOID:0050731 | vitamin B12 deficiency | MGI:1928893 | Mus musculus (house mouse) | 56546 | Sec1 |
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| DOID:10787 | premature menopause | ZFIN:ZDB-GENE-050913-15 | Danio rerio (zebrafish) | 565316 | dgat2 |
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| DOID:784 | chronic kidney disease | ZFIN:ZDB-GENE-050913-15 | Danio rerio (zebrafish) | 565316 | dgat2 |
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| DOID:9452 | steatotic liver disease | ZFIN:ZDB-GENE-050913-15 | Danio rerio (zebrafish) | 565316 | dgat2 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | ZFIN:ZDB-GENE-050913-15 | Danio rerio (zebrafish) | 565316 | dgat2 |
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| DOID:987 | alopecia | HGNC:9491 | Homo sapiens (human) | 5652 | PRSS8 |
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| DOID:8634 | prostate carcinoma in situ | HGNC:9491 | Homo sapiens (human) | 5652 | PRSS8 |
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| DOID:2394 | ovarian cancer | HGNC:9491 | Homo sapiens (human) | 5652 | PRSS8 |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | HGNC:9491 | Homo sapiens (human) | 5652 | PRSS8 |
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| DOID:3459 | breast carcinoma | HGNC:9491 | Homo sapiens (human) | 5652 | PRSS8 |
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| DOID:0060575 | 3MC syndrome 1 | HGNC:6901 | Homo sapiens (human) | 5648 | MASP1 |
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| DOID:0050589 | inflammatory bowel disease | ZFIN:ZDB-GENE-041014-160 | Danio rerio (zebrafish) | 564336 | st6galnac1.1 |
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| DOID:2747 | glycogen storage disease | MGI:1891833 | Mus musculus (house mouse) | 56421 | Pfkp |
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| DOID:0014667 | disease of metabolism | MGI:1891833 | Mus musculus (house mouse) | 56421 | Pfkp |
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