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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 5976 - 6000 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:4450 renal cell carcinoma HGNC:6015 Homo sapiens (human) 3566 IL4R inference by association of genotype from phenotype used in manual assertion
  • PMID:12171893
  • PMID:22317767
DOID:2841 asthma HGNC:6015 Homo sapiens (human) 3566 IL4R inference by association of genotype from phenotype used in manual assertion
  • PMID:11709756
  • PMID:12133990
  • PMID:12940513
  • PMID:15479272
  • PMID:17170387
  • PMID:17586032
  • PMID:17823973
  • PMID:18425216
  • PMID:20868478
DOID:3082 interstitial lung disease HGNC:6015 Homo sapiens (human) 3566 IL4R direct assay evidence used in manual assertion
  • PMID:15161635
DOID:11204 allergic conjunctivitis HGNC:6015 Homo sapiens (human) 3566 IL4R inference by association of genotype from phenotype used in manual assertion
  • PMID:20002627
DOID:11963 esophagitis HGNC:6015 Homo sapiens (human) 3566 IL4R inference by association of genotype from phenotype used in manual assertion
  • PMID:20811626
DOID:3310 atopic dermatitis HGNC:6015 Homo sapiens (human) 3566 IL4R inference by association of genotype from phenotype used in manual assertion
  • PMID:9392697
DOID:0050784 primary progressive multiple sclerosis HGNC:6015 Homo sapiens (human) 3566 IL4R inference by association of genotype from phenotype used in manual assertion
  • PMID:11164908
DOID:9733 renal tuberculosis HGNC:6015 Homo sapiens (human) 3566 IL4R inference by association of genotype from phenotype used in manual assertion
  • PMID:19548368
DOID:2377 multiple sclerosis HGNC:6014 Homo sapiens (human) 3565 IL4 inference by association of genotype from phenotype used in manual assertion
  • PMID:9184650
DOID:2841 asthma HGNC:6014 Homo sapiens (human) 3565 IL4 inference by association of genotype from phenotype used in manual assertion
  • PMID:21103062
DOID:10652 Alzheimer's disease HGNC:6014 Homo sapiens (human) 3565 IL4 inference by association of genotype from phenotype used in manual assertion
  • PMID:20213229
DOID:0050625 biliary tract benign neoplasm HGNC:6014 Homo sapiens (human) 3565 IL4 mutant phenotype evidence used in manual assertion
  • PMID:18798553
DOID:13375 temporal arteritis HGNC:6014 Homo sapiens (human) 3565 IL4 inference by association of genotype from phenotype used in manual assertion
  • PMID:15570643
DOID:1883 hepatitis C HGNC:6014 Homo sapiens (human) 3565 IL4 inference by association of genotype from phenotype used in manual assertion
  • PMID:28368861
DOID:2048 autoimmune hepatitis HGNC:6014 Homo sapiens (human) 3565 IL4 inference by association of genotype from phenotype used in manual assertion
  • PMID:26735262
DOID:3587 pancreatic ductal carcinoma HGNC:6014 Homo sapiens (human) 3565 IL4 mutant phenotype evidence used in manual assertion
  • PMID:17942922
DOID:13241 Behcet's disease HGNC:6014 Homo sapiens (human) 3565 IL4 inference by association of genotype from phenotype used in manual assertion
  • PMID:21640045
DOID:0080822 aspirin-induced respiratory disease HGNC:6014 Homo sapiens (human) 3565 IL4 inference by association of genotype from phenotype used in manual assertion
  • PMID:20921925
DOID:2043 hepatitis B HGNC:6014 Homo sapiens (human) 3565 IL4 inference by association of genotype from phenotype used in manual assertion
  • PMID:28051794
DOID:1793 pancreatic cancer HGNC:6014 Homo sapiens (human) 3565 IL4 mutant phenotype evidence used in manual assertion
  • PMID:12097255
DOID:8924 autoimmune thrombocytopenic purpura HGNC:6014 Homo sapiens (human) 3565 IL4 inference by association of genotype from phenotype used in manual assertion
  • PMID:25051072
DOID:3310 atopic dermatitis HGNC:6014 Homo sapiens (human) 3565 IL4 inference by association of genotype from phenotype used in manual assertion
  • PMID:9643293
DOID:2841 asthma HGNC:6011 Homo sapiens (human) 3562 IL3 inference by association of genotype from phenotype used in manual assertion
  • PMID:15372320
  • PMID:24684517
DOID:12361 Graves' disease HGNC:6011 Homo sapiens (human) 3562 IL3 inference by association of genotype from phenotype used in manual assertion
  • PMID:20332709
DOID:7148 rheumatoid arthritis HGNC:6011 Homo sapiens (human) 3562 IL3 inference by association of genotype from phenotype used in manual assertion
  • PMID:20018070
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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