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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:0050567 | orofacial cleft | HGNC:15814 | Homo sapiens (human) | 55902 | ACSS2 |
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| DOID:1574 | alcohol use disorder | HGNC:15814 | Homo sapiens (human) | 55902 | ACSS2 |
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| DOID:3319 | lymphangioleiomyomatosis | HGNC:15814 | Homo sapiens (human) | 55902 | ACSS2 |
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| DOID:11981 | morbid obesity | HGNC:15814 | Homo sapiens (human) | 55902 | ACSS2 |
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| DOID:409 | liver disease | HGNC:9411 | Homo sapiens (human) | 5589 | PRKCSH |
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| DOID:0050770 | polycystic liver disease | HGNC:9411 | Homo sapiens (human) | 5589 | PRKCSH |
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| DOID:0110777 | hereditary spastic paraplegia 26 | ZFIN:ZDB-GENE-070112-1462 | Danio rerio (zebrafish) | 558684 | b4galnt1a |
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| DOID:0070263 | congenital disorder of glycosylation type IIk | HGNC:30760 | Homo sapiens (human) | 55858 | TMEM165 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:30760 | Homo sapiens (human) | 55858 | TMEM165 |
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| DOID:0050589 | inflammatory bowel disease | HGNC:23614 | Homo sapiens (human) | 55808 | ST6GALNAC1 |
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| DOID:10273 | heart conduction disease | HGNC:15460 | Homo sapiens (human) | 55799 | CACNA2D3 |
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| DOID:1059 | intellectual disability | ZFIN:ZDB-GENE-090109-2 | Danio rerio (zebrafish) | 557801 | il1rapl1b |
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| DOID:0112022 | non-syndromic X-linked intellectual disability 21 | ZFIN:ZDB-GENE-090109-2 | Danio rerio (zebrafish) | 557801 | il1rapl1b |
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| DOID:0060728 | NGLY1-deficiency | HGNC:17646 | Homo sapiens (human) | 55768 | NGLY1 |
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| DOID:0060050 | autoimmune disease of blood | ZFIN:ZDB-GENE-061013-303 | Danio rerio (zebrafish) | 557675 | c1galt1la |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | HGNC:25590 | Homo sapiens (human) | 55753 | OGDHL |
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| DOID:0081326 | oxoglutarate dehydrogenase deficiency | HGNC:25590 | Homo sapiens (human) | 55753 | OGDHL |
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| DOID:0110245 | cataract 38 | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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| DOID:0080132 | Sengers syndrome | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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| DOID:1094 | attention deficit hyperactivity disorder | ZFIN:ZDB-GENE-041001-163 | Danio rerio (zebrafish) | 557218 | usta |
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| DOID:0111239 | congenital muscular dystrophy-dystroglycanopathy type A10 | ZFIN:ZDB-GENE-060929-1018 | Danio rerio (zebrafish) | 557187 | rxylt1 |
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| DOID:0050560 | Walker-Warburg syndrome | ZFIN:ZDB-GENE-060929-1018 | Danio rerio (zebrafish) | 557187 | rxylt1 |
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| DOID:0080470 | developmental and epileptic encephalopathy 36 | ZFIN:ZDB-GENE-060307-1 | Danio rerio (zebrafish) | 557181 | alg13 |
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| DOID:987 | alopecia | HGNC:25531 | Homo sapiens (human) | 55711 | FAR2 |
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| DOID:10140 | dry eye syndrome | HGNC:25531 | Homo sapiens (human) | 55711 | FAR2 |
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