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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 5876 - 5900 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:2349 arteriosclerosis HGNC:603 Homo sapiens (human) 338 APOB mutant phenotype evidence used in manual assertion
  • PMID:19260948
DOID:4606 bile duct cancer HGNC:603 Homo sapiens (human) 338 APOB inference by association of genotype from phenotype used in manual assertion
  • PMID:18296645
DOID:0111062 familial hypobetalipoproteinemia 1 HGNC:603 Homo sapiens (human) 338 APOB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1168 familial hyperlipidemia HGNC:603 Homo sapiens (human) 338 APOB inference by association of genotype from phenotype used in manual assertion
  • PMID:7627691
DOID:13810 familial hypercholesterolemia HGNC:603 Homo sapiens (human) 338 APOB inference by association of genotype from phenotype used in manual assertion
  • PMID:3627182
  • PMID:9603795
  • RGD:7240710
DOID:8947 diabetic retinopathy HGNC:603 Homo sapiens (human) 338 APOB direct assay evidence used in manual assertion
  • PMID:19448981
DOID:9352 type 2 diabetes mellitus HGNC:603 Homo sapiens (human) 338 APOB direct assay evidence used in manual assertion
  • PMID:15161783
DOID:3121 gallbladder cancer HGNC:603 Homo sapiens (human) 338 APOB inference by association of genotype from phenotype used in manual assertion
  • PMID:17696941
  • PMID:20082485
DOID:2394 ovarian cancer HGNC:603 Homo sapiens (human) 338 APOB direct assay evidence used in manual assertion
  • PMID:9023386
DOID:1390 hypobetalipoproteinemia HGNC:603 Homo sapiens (human) 338 APOB inference by association of genotype from phenotype used in manual assertion
  • PMID:3473077
DOID:10923 sickle cell anemia HGNC:603 Homo sapiens (human) 338 APOB direct assay evidence used in manual assertion
  • PMID:24035168
DOID:1712 aortic valve stenosis HGNC:603 Homo sapiens (human) 338 APOB inference by association of genotype from phenotype used in manual assertion
  • PMID:11903341
DOID:1273 respiratory syncytial virus infectious disease HGNC:6029 Homo sapiens (human) 3578 IL9 inference by association of genotype from phenotype used in manual assertion
  • PMID:20503287
DOID:2841 asthma HGNC:6029 Homo sapiens (human) 3578 IL9 mutant phenotype evidence used in manual assertion
  • PMID:21356110
DOID:2986 IgA glomerulonephritis HGNC:6027 Homo sapiens (human) 3579 CXCR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21214373
DOID:783 end stage renal disease HGNC:6027 Homo sapiens (human) 3579 CXCR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:23615182
DOID:0060973 WHIM syndrome 2 HGNC:6027 Homo sapiens (human) 3579 CXCR2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11054 urinary bladder cancer HGNC:6027 Homo sapiens (human) 3579 CXCR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:19252927
DOID:559 acute pyelonephritis HGNC:6027 Homo sapiens (human) 3579 CXCR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:22325052
DOID:11400 pyelonephritis HGNC:6026 Homo sapiens (human) 3577 CXCR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17786197
  • PMID:22325052
DOID:526 human immunodeficiency virus infectious disease HGNC:6026 Homo sapiens (human) 3577 CXCR1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080784 urinary tract infection HGNC:6026 Homo sapiens (human) 3577 CXCR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21151974
DOID:219 colon cancer HGNC:6024 Homo sapiens (human) 3575 IL7R inference by association of genotype from phenotype used in manual assertion
  • PMID:29755661
DOID:10534 stomach cancer HGNC:6024 Homo sapiens (human) 3575 IL7R inference by association of genotype from phenotype used in manual assertion
  • PMID:18687755
DOID:612 primary immunodeficiency disease HGNC:6024 Homo sapiens (human) 3575 IL7R inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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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