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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 13151 - 13175 of 14279 in total
Disease ID Disease Name ▲ Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:1749 squamous cell carcinoma HGNC:6001 Homo sapiens (human) 3558 IL2 direct assay evidence used in manual assertion
  • PMID:11023201
DOID:1749 squamous cell carcinoma HGNC:8101 Homo sapiens (human) 4948 OCA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:24617981
DOID:1749 squamous cell carcinoma HGNC:13861 Homo sapiens (human) 11178 LZTS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10097140
DOID:1749 squamous cell carcinoma HGNC:2505 Homo sapiens (human) 1493 CTLA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:19622768
DOID:1749 squamous cell carcinoma HGNC:11364 Homo sapiens (human) 6774 STAT3 direct assay evidence used in manual assertion
  • PMID:16043897
DOID:3168 squamous cell neoplasm HGNC:30796 Homo sapiens (human) 11171 STRAP direct assay evidence used in manual assertion
  • PMID:16778189
DOID:1824 status epilepticus RGD:2143 Rattus norvegicus (Norway rat) 25293 Aqp4 mutant phenotype evidence used in manual assertion
  • PMID:20886625
DOID:1824 status epilepticus RGD:3342 Rattus norvegicus (Norway rat) 25692 Plat direct assay evidence used in manual assertion
  • PMID:17040480
DOID:1824 status epilepticus HGNC:1033 Homo sapiens (human) 627 BDNF mutant phenotype evidence used in manual assertion
  • PMID:19686240
DOID:1824 status epilepticus RGD:620349 Rattus norvegicus (Norway rat) 29527 Ptgs2 mutant phenotype evidence used in manual assertion
  • PMID:20643531
DOID:1824 status epilepticus RGD:2732 Rattus norvegicus (Norway rat) 29559 Grik1 direct assay evidence used in manual assertion
  • PMID:12724156
DOID:1824 status epilepticus RGD:620458 Rattus norvegicus (Norway rat) 89808 Cx3cl1 mutant phenotype evidence used in manual assertion
  • PMID:21481949
DOID:1824 status epilepticus RGD:1597139 Rattus norvegicus (Norway rat) 361596 Idh2 direct assay evidence used in manual assertion
  • PMID:29778462
DOID:1824 status epilepticus RGD:620486 Rattus norvegicus (Norway rat) 59323 Erbb4 direct assay evidence used in manual assertion
  • PMID:22158510
DOID:1824 status epilepticus RGD:2202 Rattus norvegicus (Norway rat) 24225 Bdnf mutant phenotype evidence used in manual assertion
  • PMID:19366663
  • PMID:19686240
DOID:0111556 steatocystoma multiplex HGNC:6427 Homo sapiens (human) 3872 KRT17 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9452 steatotic liver disease RGD:2670 Rattus norvegicus (Norway rat) 24385 Gck direct assay evidence used in manual assertion
  • PMID:22925001
DOID:9452 steatotic liver disease SGD:S000000995 Saccharomyces cerevisiae S288C 856386 LAG1 sequence similarity evidence used in manual assertion
  • PMID:29626628
DOID:9452 steatotic liver disease RGD:620925 Rattus norvegicus (Norway rat) 83516 Ppargc1a direct assay evidence used in manual assertion
  • PMID:23274094
DOID:9452 steatotic liver disease HGNC:5293 Homo sapiens (human) 3356 HTR2A inference by association of genotype from phenotype used in manual assertion
  • PMID:33081272
DOID:9452 steatotic liver disease HGNC:2631 Homo sapiens (human) 1571 CYP2E1 inference by association of genotype from phenotype used in manual assertion
  • PMID:14606109
DOID:9452 steatotic liver disease MGI:96765 Mus musculus (house mouse) 16835 Ldlr author statement supported by traceable reference
  • PMID:21690266
DOID:9452 steatotic liver disease HGNC:286 Homo sapiens (human) 154 ADRB2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11718682
DOID:9452 steatotic liver disease HGNC:5294 Homo sapiens (human) 3357 HTR2B inference by association of genotype from phenotype used in manual assertion
  • PMID:33081272
DOID:9452 steatotic liver disease HGNC:4801 Homo sapiens (human) 3030 HADHA inference by association of genotype from phenotype used in manual assertion
  • PMID:7846063
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Supported by JST NBDC Grant Number JPMJND2204

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

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Last updated: December 8, 2025