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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 January 28, 2025
Displaying entries 2626 - 2650 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:0112207 developmental and epileptic encephalopathy 71 HGNC:4331 Homo sapiens (human) 2744 GLS inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110284 autosomal recessive limb-girdle muscular dystrophy type 2L HGNC:27337 Homo sapiens (human) 203859 ANO5 inference by association of genotype from phenotype used in manual assertion
  • PMID:20096397
  • PMID:22742934
  • PMID:23606453
  • RGD:7240710
DOID:0080291 developmental and epileptic encephalopathy 59 HGNC:4507 Homo sapiens (human) 9568 GABBR2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:13580 cholestasis HGNC:12712 Homo sapiens (human) 26276 VPS33B inference by association of genotype from phenotype used in manual assertion
  • PMID:15052268
DOID:10783 methemoglobinemia HGNC:2873 Homo sapiens (human) 1727 CYB5R3 inference by association of genotype from phenotype used in manual assertion
  • PMID:11295830
DOID:13141 uveitis HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12198697
  • PMID:16495319
DOID:10652 Alzheimer's disease HGNC:934 Homo sapiens (human) 25825 BACE2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16023140
DOID:3908 lung non-small cell carcinoma HGNC:3431 Homo sapiens (human) 2065 ERBB3 mutant phenotype evidence used in manual assertion
  • PMID:20364069
DOID:83 cataract HGNC:381 Homo sapiens (human) 231 AKR1B1 mutant phenotype evidence used in manual assertion
  • PMID:21329682
DOID:3144 cutis laxa HGNC:3602 Homo sapiens (human) 10516 FBLN5 inference by association of genotype from phenotype used in manual assertion
  • PMID:12189163
DOID:10763 hypertension HGNC:6145 Homo sapiens (human) 3680 ITGA9 inference by association of genotype from phenotype used in manual assertion
  • PMID:20479155
DOID:684 hepatocellular carcinoma HGNC:9948 Homo sapiens (human) 5965 RECQL mutant phenotype evidence used in manual assertion
  • PMID:18422747
DOID:0060691 platelet-type bleeding disorder 16 HGNC:6138 Homo sapiens (human) 3674 ITGA2B inference by association of genotype from phenotype used in manual assertion
  • PMID:19691478
  • PMID:21029361
  • PMID:22394243
  • RGD:7240710
DOID:0080162 lupus nephritis HGNC:3616 Homo sapiens (human) 2212 FCGR2A inference by association of genotype from phenotype used in manual assertion
  • PMID:15004265
DOID:14115 toxic shock syndrome HGNC:775 Homo sapiens (human) 462 SERPINC1 direct assay evidence used in manual assertion
  • PMID:16732381
DOID:10754 otitis media HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:17908769
DOID:9620 vesicoureteral reflux HGNC:10250 Homo sapiens (human) 6092 ROBO2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3312 bipolar disorder HGNC:7997 Homo sapiens (human) 3084 NRG1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18585932
DOID:3907 lung squamous cell carcinoma HGNC:4553 Homo sapiens (human) 2876 GPX1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16797832
  • PMID:18298806
DOID:768 retinoblastoma HGNC:8824 Homo sapiens (human) 5176 SERPINF1 direct assay evidence used in manual assertion
  • PMID:19832843
DOID:3310 atopic dermatitis HGNC:613 Homo sapiens (human) 348 APOE direct assay evidence used in manual assertion
  • PMID:19116453
DOID:10591 pre-eclampsia HGNC:11892 Homo sapiens (human) 7124 TNF inference by association of genotype from phenotype used in manual assertion
  • PMID:15901845
DOID:0110354 retinitis pigmentosa 19 HGNC:34 Homo sapiens (human) 24 ABCA4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050861 colorectal adenocarcinoma HGNC:5331 Homo sapiens (human) 64127 NOD2 inference by association of genotype from phenotype used in manual assertion
  • PMID:27354594
DOID:0050431 arrhythmogenic right ventricular cardiomyopathy HGNC:1759 Homo sapiens (human) 1000 CDH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:28280076
  • PMID:28326674
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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: April 7, 2025