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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 9926 - 9950 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References ▲
DOID:10591 pre-eclampsia HGNC:11621 Homo sapiens (human) 6927 HNF1A inference by association of genotype from phenotype used in manual assertion
  • PMID:31825269
DOID:9675 pulmonary emphysema MGI:102793 Mus musculus (house mouse) 14314 Fstl1 author statement supported by traceable reference
  • PMID:31834999
DOID:62 aortic valve disease MGI:2442875 Mus musculus (house mouse) 240322 Adamts19 author statement supported by traceable reference
  • PMID:31844321
DOID:526 human immunodeficiency virus infectious disease HGNC:6340 Homo sapiens (human) 3813 KIR3DS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:31863692
DOID:526 human immunodeficiency virus infectious disease HGNC:6338 Homo sapiens (human) 3811 KIR3DL1 inference by association of genotype from phenotype used in manual assertion
  • PMID:31863692
DOID:0070309 absence epilepsy ZFIN:ZDB-GENE-040724-26 Danio rerio (zebrafish) 562059 cacna1aa author statement supported by traceable reference used in manual assertion
  • PMID:31875924
DOID:162 cancer FB:FBgn0013733 Drosophila melanogaster (fruit fly) 36542 shot combinatorial experimental and author inference evidence used in manual assertion
  • PMID:31882643
DOID:11166 Human papillomavirus infectious disease HGNC:225 Homo sapiens (human) 103 ADAR inference by association of genotype from phenotype used in manual assertion
  • PMID:31882741
DOID:0050700 cardiomyopathy HGNC:7871 Homo sapiens (human) 4841 NONO inference by association of genotype from phenotype used in manual assertion
  • PMID:31883306
DOID:0050742 nicotine dependence HGNC:3025 Homo sapiens (human) 1815 DRD4 inference by association of genotype from phenotype used in manual assertion
  • PMID:31903031
DOID:0112276 neurodevelopmental disorder with involuntary movements MGI:95775 Mus musculus (house mouse) 14681 Gnao1 author statement supported by traceable reference
  • PMID:31907305
DOID:684 hepatocellular carcinoma HGNC:6866 Homo sapiens (human) 9448 MAP4K4 direct assay evidence used in manual assertion
  • PMID:31922225
DOID:784 chronic kidney disease HGNC:4553 Homo sapiens (human) 2876 GPX1 inference by association of genotype from phenotype used in manual assertion
  • PMID:31924810
DOID:219 colon cancer HGNC:391 Homo sapiens (human) 207 AKT1 mutant phenotype evidence used in manual assertion
  • PMID:31932471
DOID:9976 heroin dependence HGNC:8154 Homo sapiens (human) 4986 OPRK1 inference by association of genotype from phenotype used in manual assertion
  • PMID:31940240
DOID:693 dental enamel hypoplasia RGD:2332 Rattus norvegicus (Norway rat) 24255 Cftr mutant phenotype evidence used in manual assertion
  • PMID:31942562
DOID:0112051 non-syndromic X-linked intellectual disability 30 MGI:1339656 Mus musculus (house mouse) 18481 Pak3 author statement supported by traceable reference
  • PMID:31943058
DOID:2841 asthma RGD:1303284 Rattus norvegicus (Norway rat) 312896 Trpa1 mutant phenotype evidence used in manual assertion
  • PMID:31969645
DOID:12206 dengue hemorrhagic fever HGNC:18363 Homo sapiens (human) 282618 IFNL1 inference by association of genotype from phenotype used in manual assertion
  • PMID:31981768
DOID:0080547 metabolic dysfunction-associated steatohepatitis MGI:99457 Mus musculus (house mouse) 17202 Mc4r author statement supported by traceable reference
  • PMID:31990961
DOID:0080202 adenoid cystic carcinoma HGNC:882 Homo sapiens (human) 545 ATR mutant phenotype evidence used in manual assertion
  • PMID:32001675
DOID:3908 lung non-small cell carcinoma HGNC:7562 Homo sapiens (human) 4615 MYD88 direct assay evidence used in manual assertion
  • PMID:32010578
DOID:1826 epilepsy MGI:1928948 Mus musculus (house mouse) 56807 Scamp5 author statement supported by traceable reference
  • PMID:32020363
DOID:3969 papillary thyroid carcinoma HGNC:7133 Homo sapiens (human) 8085 KMT2D inference by association of genotype from phenotype used in manual assertion
  • PMID:32024448
DOID:332 amyotrophic lateral sclerosis HGNC:7997 Homo sapiens (human) 3084 NRG1 mutant phenotype evidence used in manual assertion
  • PMID:32032731
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Supported by JST NBDC Grant Number JPMJND2204

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