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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 10051 - 10075 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence References
DOID:0081120 Graves ophthalmopathy HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:2786308
DOID:11446 sciatic neuropathy HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:12574433
DOID:9538 multiple myeloma HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:17926179
DOID:9352 type 2 diabetes mellitus HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:17069782
  • PMID:21205020
DOID:10459 common cold HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:18279051
DOID:4371 Schnitzler syndrome HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:16096327
DOID:12554 hemolytic-uremic syndrome HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:12373296
DOID:7148 rheumatoid arthritis HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:19447938
DOID:10325 silicosis HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:11264025
DOID:824 periodontitis HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:22795294
DOID:8924 autoimmune thrombocytopenic purpura HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:20626741
DOID:986 alopecia areata HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:8077705
DOID:12894 Sjogren's syndrome HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:9646842
DOID:11382 corneal neovascularization HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:10359324
DOID:6432 pulmonary hypertension HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:7946395
DOID:11476 osteoporosis HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:8182127
DOID:13139 crescentic glomerulonephritis HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:7637259
DOID:10126 keratoconus HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:23462747
DOID:1407 anterior uveitis HGNC:6000 Homo sapiens (human) 3557 IL1RN mutant phenotype evidence used in manual assertion
  • PMID:19693263
DOID:11713 diabetic angiopathy HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10763 hypertension HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:11840488
DOID:5199 ureteral obstruction HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:21975862
DOID:1184 nephrotic syndrome HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:14758530
DOID:9744 type 1 diabetes mellitus HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:9158104
DOID:3908 lung non-small cell carcinoma HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:16126303
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Supported by JST NBDC Grant Number JPMJND2204

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