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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 5926 - 5950 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:1324 lung cancer HGNC:6407 Homo sapiens (human) 3845 KRAS inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:783 end stage renal disease HGNC:3356 Homo sapiens (human) 5167 ENPP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18184924
DOID:4959 epidermolysis bullosa dystrophica HGNC:7155 Homo sapiens (human) 4312 MMP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18030675
DOID:684 hepatocellular carcinoma HGNC:583 Homo sapiens (human) 324 APC inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060556 Kufor-Rakeb syndrome HGNC:30213 Homo sapiens (human) 23400 ATP13A2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060903 thrombosis HGNC:775 Homo sapiens (human) 462 SERPINC1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12595305
DOID:0111558 Charcot-Marie-Tooth disease type 2DD HGNC:799 Homo sapiens (human) 476 ATP1A1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110429 dilated cardiomyopathy 1H HGNC:2592 Homo sapiens (human) 1585 CYP11B2 inference by association of genotype from phenotype used in manual assertion
  • PMID:12031704
DOID:2920 membranoproliferative glomerulonephritis HGNC:3778 Homo sapiens (human) 2335 FN1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110146 Bartter disease type 4b HGNC:2027 Homo sapiens (human) 1188 CLCNKB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080286 spinocerebellar ataxia 44 HGNC:4593 Homo sapiens (human) 2911 GRM1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112196 spondylometaepiphyseal dysplasia, short limb-hand type HGNC:2731 Homo sapiens (human) 4921 DDR2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112148 Uruguay faciocardiomusculoskeletal syndrome HGNC:3702 Homo sapiens (human) 2273 FHL1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2340 craniosynostosis HGNC:11623 Homo sapiens (human) 6938 TCF12 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10534 stomach cancer HGNC:6848 Homo sapiens (human) 4214 MAP3K1 inference by association of genotype from phenotype used in manual assertion
  • PMID:23042672
  • PMID:31686841
DOID:14705 Pfeiffer syndrome HGNC:3688 Homo sapiens (human) 2260 FGFR1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3969 papillary thyroid carcinoma HGNC:7133 Homo sapiens (human) 8085 KMT2D inference by association of genotype from phenotype used in manual assertion
  • PMID:32024448
DOID:4511 breast angiosarcoma HGNC:8975 Homo sapiens (human) 5290 PIK3CA inference by association of genotype from phenotype used in manual assertion
  • PMID:32123305
DOID:9976 heroin dependence HGNC:40 Homo sapiens (human) 5243 ABCB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:29173032
DOID:8893 psoriasis HGNC:12680 Homo sapiens (human) 7422 VEGFA inference by association of genotype from phenotype used in manual assertion
  • PMID:14962110
DOID:10584 retinitis pigmentosa HGNC:17340 Homo sapiens (human) 10594 PRPF8 inference by association of genotype from phenotype used in manual assertion
  • PMID:11468273
DOID:14320 generalized anxiety disorder HGNC:11050 Homo sapiens (human) 6532 SLC6A4 inference by association of genotype from phenotype used in manual assertion
  • PMID:22907732
DOID:5844 myocardial infarction HGNC:8602 Homo sapiens (human) 5069 PAPPA inference by association of genotype from phenotype used in manual assertion
  • PMID:17700210
DOID:1793 pancreatic cancer HGNC:172 Homo sapiens (human) 91 ACVR1B inference by association of genotype from phenotype used in manual assertion
  • PMID:11248065
  • RGD:7240710
DOID:4428 dyslexia HGNC:13875 Homo sapiens (human) 93986 FOXP2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21897444
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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