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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 9901 - 9925 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence References
DOID:3495 extrahepatic bile duct adenocarcinoma HGNC:30064 Homo sapiens (human) 55193 PBRM1 inference by association of genotype from phenotype used in manual assertion
  • PMID:25536104
DOID:3908 lung non-small cell carcinoma HGNC:30064 Homo sapiens (human) 55193 PBRM1 inference by association of genotype from phenotype used in manual assertion
  • PMID:32195359
DOID:5409 lung small cell carcinoma HGNC:30064 Homo sapiens (human) 55193 PBRM1 inference by association of genotype from phenotype used in manual assertion
  • PMID:29748005
DOID:3651 pyruvate carboxylase deficiency disease HGNC:8636 Homo sapiens (human) 5091 PC inference by association of genotype from phenotype used in manual assertion
  • PMID:9585612
  • RGD:7240710
DOID:14701 propionic acidemia HGNC:8653 Homo sapiens (human) 5095 PCCA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9252 amino acid metabolic disorder HGNC:8653 Homo sapiens (human) 5095 PCCA inference by association of genotype from phenotype used in manual assertion
  • PMID:9385377
DOID:14701 propionic acidemia HGNC:8654 Homo sapiens (human) 5096 PCCB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9252 amino acid metabolic disorder HGNC:8654 Homo sapiens (human) 5096 PCCB inference by association of genotype from phenotype used in manual assertion
  • PMID:8411997
DOID:0110831 Usher syndrome type 1D HGNC:14674 Homo sapiens (human) 65217 PCDH15 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110832 Usher syndrome type 1F HGNC:14674 Homo sapiens (human) 65217 PCDH15 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110481 autosomal recessive nonsyndromic deafness 23 HGNC:14674 Homo sapiens (human) 65217 PCDH15 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060848 developmental and epileptic encephalopathy 9 HGNC:14270 Homo sapiens (human) 57526 PCDH19 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:8724 Homo sapiens (human) 5105 PCK1 inference by association of genotype from phenotype used in manual assertion
  • PMID:19070910
DOID:10652 Alzheimer's disease HGNC:8724 Homo sapiens (human) 5105 PCK1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17440948
  • PMID:20574532
DOID:0060272 pontocerebellar hypoplasia type 3 HGNC:13406 Homo sapiens (human) 27445 PCLO inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:162 cancer SGD:S000000784 Saccharomyces cerevisiae S288C 856652 PCM1 sequence similarity evidence used in manual assertion
  • PMID:26354769
DOID:162 cancer SGD:S000000784 Saccharomyces cerevisiae S288C 856652 PCM1 genetic interaction evidence used in manual assertion
  • PMID:26354769
DOID:0081385 ataxia-telangiectasia-like disorder-2 HGNC:8729 Homo sapiens (human) 5111 PCNA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060609 microcephalic osteodysplastic primordial dwarfism type II HGNC:16068 Homo sapiens (human) 5116 PCNT inference by association of genotype from phenotype used in manual assertion
  • PMID:18157127
  • PMID:18174396
  • PMID:19643772
  • PMID:21567919
  • RGD:7240710
DOID:9970 obesity HGNC:8743 Homo sapiens (human) 5122 PCSK1 inference by association of genotype from phenotype used in manual assertion
  • PMID:9207799
DOID:0111698 proprotein convertase 1/3 deficiency HGNC:8743 Homo sapiens (human) 5122 PCSK1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:8744 Homo sapiens (human) 5126 PCSK2 inference by association of genotype from phenotype used in manual assertion
  • PMID:7698505
DOID:5844 myocardial infarction HGNC:8744 Homo sapiens (human) 5126 PCSK2 inference by association of genotype from phenotype used in manual assertion
  • PMID:20036365
DOID:0050861 colorectal adenocarcinoma HGNC:8746 Homo sapiens (human) 54760 PCSK4 inference by association of genotype from phenotype used in manual assertion
  • PMID:27354594
DOID:1390 hypobetalipoproteinemia HGNC:20001 Homo sapiens (human) 255738 PCSK9 inference by association of genotype from phenotype used in manual assertion
  • PMID:16619215
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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: April 7, 2025