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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 9876 - 9900 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References ▲
DOID:9256 colorectal cancer HGNC:2745 Homo sapiens (human) 1654 DDX3X mutant phenotype evidence used in manual assertion
  • PMID:31391454
DOID:0070561 glucose transporter type 1 deficiency syndrome 1 MGI:95755 Mus musculus (house mouse) 20525 Slc2a1 author statement supported by traceable reference
  • PMID:31399478
DOID:10914 amnestic disorder RGD:620218 Rattus norvegicus (Norway rat) 81646 Creb1 direct assay evidence used in manual assertion
  • PMID:31400468
DOID:684 hepatocellular carcinoma HGNC:5021 Homo sapiens (human) 3169 FOXA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:31400761
DOID:0050921 pharynx squamous cell carcinoma HGNC:24308 Homo sapiens (human) 81037 CLPTM1L inference by association of genotype from phenotype used in manual assertion
  • PMID:31429604
DOID:1495 cystic echinococcosis HGNC:11848 Homo sapiens (human) 7097 TLR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:31437685
DOID:0050776 non-syndromic X-linked intellectual disability MGI:3528396 Mus musculus (house mouse) 245666 Iqsec2 author statement supported by traceable reference
  • PMID:31439632
  • PMID:31978606
DOID:0112247 congenital heart defects, dysmorphic facial features, and intellectual developmental disorder MGI:1916812 Mus musculus (house mouse) 69562 Cdk13 author statement supported by traceable reference
  • PMID:31440507
DOID:6432 pulmonary hypertension HGNC:435 Homo sapiens (human) 240 ALOX5 genetic interaction evidence used in manual assertion
  • PMID:31462075
DOID:3652 Leigh disease MGI:1913302 Mus musculus (house mouse) 66052 Sdhc author statement supported by traceable reference
  • PMID:31469588
DOID:162 cancer SGD:S000001085 Saccharomyces cerevisiae S288C 856439 DOG2 mutant phenotype evidence used in manual assertion
  • PMID:31481524
DOID:162 cancer SGD:S000001085 Saccharomyces cerevisiae S288C 856439 DOG2 sequence similarity evidence used in manual assertion
  • PMID:31481524
DOID:0080202 adenoid cystic carcinoma HGNC:13726 Homo sapiens (human) 58508 KMT2C inference by association of genotype from phenotype used in manual assertion
  • PMID:31483290
DOID:2152 ovary epithelial cancer HGNC:17075 Homo sapiens (human) 23118 TAB2 inference by association of genotype from phenotype used in manual assertion
  • PMID:31485280
DOID:0060041 autism spectrum disorder MGI:2441908 Mus musculus (house mouse) 319352 Pianp author statement supported by traceable reference
  • PMID:31511635
DOID:12930 dilated cardiomyopathy RGD:68380 Rattus norvegicus (Norway rat) 59106 Ltbp2 mutant phenotype evidence used in manual assertion
  • PMID:31512380
DOID:687 hepatoblastoma HGNC:7107 Homo sapiens (human) 4288 MKI67 direct assay evidence used in manual assertion
  • PMID:31541079
DOID:687 hepatoblastoma HGNC:3002 Homo sapiens (human) 1800 DPEP1 mutant phenotype evidence used in manual assertion
  • PMID:31541079
DOID:14504 Niemann-Pick disease SGD:S000005927 Saccharomyces cerevisiae S288C 856101 NCR1 mutant phenotype evidence used in manual assertion
  • PMID:31543266
  • PMID:37908116
DOID:684 hepatocellular carcinoma HGNC:7782 Homo sapiens (human) 4780 NFE2L2 direct assay evidence used in manual assertion
  • PMID:31546024
DOID:224 transient cerebral ischemia HGNC:7997 Homo sapiens (human) 3084 NRG1 mutant phenotype evidence used in manual assertion
  • PMID:31560696
DOID:3347 osteosarcoma HGNC:2561 Homo sapiens (human) 7852 CXCR4 mutant phenotype evidence used in manual assertion
  • PMID:31571016
DOID:9351 diabetes mellitus WB:WBGene00003858 Caenorhabditis elegans 176000 ogt-1 combinatorial experimental and author inference evidence used in manual assertion
  • PMID:31576392
DOID:9351 diabetes mellitus WB:WBGene00003858 Caenorhabditis elegans 176000 ogt-1 mutant phenotype evidence used in manual assertion
  • PMID:31576392
DOID:399 tuberculosis HGNC:7782 Homo sapiens (human) 4780 NFE2L2 inference by association of genotype from phenotype used in manual assertion
  • PMID:31586142
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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: April 7, 2025