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 |
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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 |
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DOID:9352 | type 2 diabetes mellitus | HGNC:11621 | Homo sapiens (human) | 6927 | HNF1A |
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DOID:9074 | systemic lupus erythematosus | HGNC:2956 | Homo sapiens (human) | 1773 | DNASE1 |
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DOID:0060900 | Parkinson's disease 14 | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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DOID:0070247 | autosomal dominant Emery-Dreifuss muscular dystrophy 2 | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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DOID:0110497 | autosomal recessive nonsyndromic deafness 39 | HGNC:4893 | Homo sapiens (human) | 3082 | HGF |
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DOID:10763 | hypertension | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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DOID:12803 | Sly syndrome | HGNC:4696 | Homo sapiens (human) | 2990 | GUSB |
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DOID:2962 | Cockayne syndrome | HGNC:3438 | Homo sapiens (human) | 2074 | ERCC6 |
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DOID:0060688 | arteriovenous malformations of the brain | HGNC:3349 | Homo sapiens (human) | 2022 | ENG |
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DOID:2908 | Treacher Collins syndrome | HGNC:11654 | Homo sapiens (human) | 6949 | TCOF1 |
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DOID:0080552 | congenital disorder of glycosylation Ia | HGNC:9115 | Homo sapiens (human) | 5373 | PMM2 |
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DOID:0110156 | Charcot-Marie-Tooth disease type 2B1 | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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DOID:0111066 | congenital bile acid synthesis defect 5 | HGNC:67 | Homo sapiens (human) | 5825 | ABCD3 |
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DOID:0110334 | osteogenesis imperfecta type 1 | HGNC:2197 | Homo sapiens (human) | 1277 | COL1A1 |
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DOID:0060810 | syndromic X-linked intellectual disability type 10 | HGNC:4800 | Homo sapiens (human) | 3028 | HSD17B10 |
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DOID:0050629 | Aicardi-Goutieres syndrome | HGNC:15925 | Homo sapiens (human) | 25939 | SAMHD1 |
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DOID:0060903 | thrombosis | HGNC:775 | Homo sapiens (human) | 462 | SERPINC1 |
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DOID:3650 | lactic acidosis | RGD:620687 | Rattus norvegicus (Norway rat) | 64035 | Pygl |
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DOID:14504 | Niemann-Pick disease | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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DOID:0060733 | junctional epidermolysis bullosa with pyloric atresia | HGNC:6158 | Homo sapiens (human) | 3691 | ITGB4 |
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DOID:594 | panic disorder | HGNC:5286 | Homo sapiens (human) | 3350 | HTR1A |
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DOID:0080154 | short chain acyl-CoA dehydrogenase deficiency | HGNC:90 | Homo sapiens (human) | 35 | ACADS |
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DOID:1287 | cardiovascular system disease | HGNC:320 | Homo sapiens (human) | 177 | AGER |
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DOID:14451 | hyperkalemic periodic paralysis | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
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DOID:0111194 | autosomal dominant adult-onset proximal spinal muscular atrophy | HGNC:12649 | Homo sapiens (human) | 9217 | VAPB |
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
GlyCosmos Portal v4.1.1
Last updated: February 17, 2025