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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:0110207 Charcot-Marie-Tooth disease X-linked dominant 6 HGNC:8811 Homo sapiens (human) 5165 PDK3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9970 obesity HGNC:9279 Homo sapiens (human) 54704 PDP1 direct assay evidence used in manual assertion
  • PMID:15897476
DOID:3649 pyruvate decarboxylase deficiency HGNC:9279 Homo sapiens (human) 54704 PDP1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10283 prostate cancer HGNC:8816 Homo sapiens (human) 5170 PDPK1 mutant phenotype evidence used in manual assertion
  • PMID:26294745
DOID:0061003 pancreatic agenesis 1 HGNC:6107 Homo sapiens (human) 3651 PDX1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:6107 Homo sapiens (human) 3651 PDX1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10545531
  • RGD:7240710
DOID:4195 hyperglycemia HGNC:6107 Homo sapiens (human) 3651 PDX1 mutant phenotype evidence used in manual assertion
  • PMID:17131142
DOID:0111103 maturity-onset diabetes of the young type 4 HGNC:6107 Homo sapiens (human) 3651 PDX1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3526 cerebral infarction HGNC:6107 Homo sapiens (human) 3651 PDX1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18506375
DOID:0110838 Usher syndrome type 2A HGNC:26257 Homo sapiens (human) 79955 PDZD7 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111635 autosomal recessive nonsyndromic deafness 57 HGNC:26257 Homo sapiens (human) 79955 PDZD7 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110839 Usher syndrome type 2C HGNC:26257 Homo sapiens (human) 79955 PDZD7 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10283 prostate cancer HGNC:8630 Homo sapiens (human) 5037 PEBP1 mutant phenotype evidence used in manual assertion
  • PMID:18722266
DOID:9008 psoriatic arthritis HGNC:8823 Homo sapiens (human) 5175 PECAM1 direct assay evidence used in manual assertion
  • PMID:22751595
DOID:3393 coronary artery disease HGNC:8823 Homo sapiens (human) 5175 PECAM1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11795274
  • PMID:12732396
DOID:5844 myocardial infarction HGNC:8823 Homo sapiens (human) 5175 PECAM1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11795274
  • PMID:15488875
DOID:4248 coronary stenosis HGNC:8823 Homo sapiens (human) 5175 PECAM1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10571959
DOID:769 neuroblastoma HGNC:8823 Homo sapiens (human) 5175 PECAM1 direct assay evidence used in manual assertion
  • PMID:22174364
DOID:0050741 alcohol dependence HGNC:8846 Homo sapiens (human) 8864 PER2 direct assay evidence used in manual assertion
  • PMID:31329297
DOID:9975 cocaine dependence HGNC:8846 Homo sapiens (human) 8864 PER2 inference by association of genotype from phenotype used in manual assertion
  • PMID:22832851
DOID:0110011 advanced sleep phase syndrome 1 HGNC:8846 Homo sapiens (human) 8864 PER2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050628 advanced sleep phase syndrome HGNC:8846 Homo sapiens (human) 8864 PER2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11232563
DOID:0050696 fetal alcohol spectrum disorder HGNC:8846 Homo sapiens (human) 8864 PER2 direct assay evidence used in manual assertion
  • PMID:31329297
DOID:3312 bipolar disorder HGNC:8847 Homo sapiens (human) 8863 PER3 inference by association of genotype from phenotype used in manual assertion
  • PMID:30121446
DOID:0050628 advanced sleep phase syndrome HGNC:8847 Homo sapiens (human) 8863 PER3 inference by association of genotype from phenotype used in manual assertion
  • PMID:11306557

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: March 31, 2025