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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 9976 - 10000 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References ▲
DOID:218 ascending colon cancer HGNC:18505 Homo sapiens (human) 54894 RNF43 inference by association of genotype from phenotype used in manual assertion
  • PMID:32236609
DOID:0080462 developmental and epileptic encephalopathy 7 MGI:1309503 Mus musculus (house mouse) 16536 Kcnq2 author statement supported by traceable reference
  • PMID:32239694
DOID:0110371 retinitis pigmentosa 56 MGI:3044955 Mus musculus (house mouse) 224224 Impg2 author statement supported by traceable reference
  • PMID:32242237
DOID:0050661 vitelliform macular dystrophy MGI:3044955 Mus musculus (house mouse) 224224 Impg2 author statement supported by traceable reference
  • PMID:32265257
DOID:0080600 COVID-19 HGNC:9071 Homo sapiens (human) 5340 PLG direct assay evidence used in manual assertion
  • PMID:32275753
DOID:11162 respiratory failure HGNC:17859 Homo sapiens (human) 23511 NUP188 inference by association of genotype from phenotype used in manual assertion
  • PMID:32275884
DOID:684 hepatocellular carcinoma HGNC:777 Homo sapiens (human) 463 ZFHX3 mutant phenotype evidence used in manual assertion
  • PMID:32277050
DOID:0080600 COVID-19 HGNC:2707 Homo sapiens (human) 1636 ACE inference by association of genotype from phenotype used in manual assertion
  • PMID:32286246
DOID:2043 hepatitis B HGNC:19191 Homo sapiens (human) 81704 DOCK8 inference by association of genotype from phenotype used in manual assertion
  • PMID:32297155
DOID:2043 hepatitis B HGNC:1383 Homo sapiens (human) 768 CA9 inference by association of genotype from phenotype used in manual assertion
  • PMID:32297155
DOID:234 colon adenocarcinoma HGNC:2433 Homo sapiens (human) 1436 CSF1R mutant phenotype evidence used in manual assertion
  • PMID:32304779
DOID:1826 epilepsy FB:FBgn0015777 Drosophila melanogaster (fruit fly) 33953 nrv2 combinatorial experimental and author inference evidence used in manual assertion
  • PMID:32344153
DOID:3748 esophagus squamous cell carcinoma HGNC:5383 Homo sapiens (human) 3418 IDH2 mutant phenotype evidence used in manual assertion
  • PMID:32367071
DOID:10534 stomach cancer HGNC:11110 Homo sapiens (human) 8289 ARID1A inference by association of genotype from phenotype used in manual assertion
  • PMID:32377988
DOID:10763 hypertension HGNC:79 Homo sapiens (human) 28 ABO inference by association of genotype from phenotype used in manual assertion
  • PMID:32379894
DOID:0080600 COVID-19 HGNC:79 Homo sapiens (human) 28 ABO inference by association of genotype from phenotype used in manual assertion
  • PMID:32379894
DOID:2237 hepatitis HGNC:79 Homo sapiens (human) 28 ABO inference by association of genotype from phenotype used in manual assertion
  • PMID:32379894
DOID:0080600 COVID-19 HGNC:13557 Homo sapiens (human) 59272 ACE2 mutant phenotype evidence used in manual assertion
  • PMID:32380511
DOID:0080600 COVID-19 HGNC:5434 Homo sapiens (human) 3456 IFNB1 direct assay evidence used in manual assertion
  • PMID:32401715
DOID:0080600 COVID-19 HGNC:4932 Homo sapiens (human) 3106 HLA-B inference by association of genotype from phenotype used in manual assertion
  • PMID:32424945
DOID:0080600 COVID-19 HGNC:4933 Homo sapiens (human) 3107 HLA-C inference by association of genotype from phenotype used in manual assertion
  • PMID:32424945
DOID:3908 lung non-small cell carcinoma HGNC:9177 Homo sapiens (human) 5426 POLE inference by association of genotype from phenotype used in manual assertion
  • PMID:32433714
DOID:0050671 female breast cancer HGNC:13723 Homo sapiens (human) 10664 CTCF inference by association of genotype from phenotype used in manual assertion
  • PMID:32435142
DOID:14330 Parkinson's disease MGI:1342774 Mus musculus (house mouse) 19017 Ppargc1a author statement supported by traceable reference
  • PMID:32439544
DOID:0080417 developmental and epileptic encephalopathy 38 SGD:S000004232 Saccharomyces cerevisiae S288C 850943 ARV1 mutant phenotype evidence used in manual assertion
  • PMID:32449190
  • PMID:32462292
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Supported by JST NBDC Grant Number JPMJND2204

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