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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 5826 - 5850 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
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:3393 coronary artery disease HGNC:610 Homo sapiens (human) 345 APOC3 inference by association of genotype from phenotype used in manual assertion
  • PMID:14709372
  • PMID:15059615
DOID:1561 cognitive disorder HGNC:610 Homo sapiens (human) 345 APOC3 inference by association of genotype from phenotype used in manual assertion
  • PMID:19424489
DOID:13809 familial combined hyperlipidemia HGNC:610 Homo sapiens (human) 345 APOC3 inference by association of genotype from phenotype used in manual assertion
  • PMID:9062353
DOID:684 hepatocellular carcinoma HGNC:610 Homo sapiens (human) 345 APOC3 inference by association of genotype from phenotype used in manual assertion
  • PMID:27547913
DOID:10603 glucose intolerance HGNC:610 Homo sapiens (human) 345 APOC3 inference by association of genotype from phenotype used in manual assertion
  • PMID:11959336
DOID:9744 type 1 diabetes mellitus HGNC:610 Homo sapiens (human) 345 APOC3 inference by association of genotype from phenotype used in manual assertion
  • PMID:16505251
DOID:3145 hyperlipoproteinemia type III HGNC:610 Homo sapiens (human) 345 APOC3 inference by association of genotype from phenotype used in manual assertion
  • PMID:2879788
DOID:0111370 apolipoprotein C-III deficiency HGNC:610 Homo sapiens (human) 345 APOC3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:784 chronic kidney disease HGNC:610 Homo sapiens (human) 345 APOC3 direct assay evidence used in manual assertion
  • PMID:21297177
DOID:10588 adrenoleukodystrophy HGNC:61 Homo sapiens (human) 215 ABCD1 inference by association of genotype from phenotype used in manual assertion
  • PMID:8048932
  • RGD:7240710
DOID:3594 choriocarcinoma HGNC:6091 Homo sapiens (human) 3643 INSR direct assay evidence used in manual assertion
  • PMID:17556377
DOID:9351 diabetes mellitus HGNC:6091 Homo sapiens (human) 3643 INSR inference by association of genotype from phenotype used in manual assertion
  • PMID:18925540
DOID:11714 gestational diabetes HGNC:6091 Homo sapiens (human) 3643 INSR direct assay evidence used in manual assertion
  • PMID:19179458
DOID:2526 prostate adenocarcinoma HGNC:6091 Homo sapiens (human) 3643 INSR mutant phenotype evidence used in manual assertion
  • PMID:26452103
DOID:0050470 Donohue syndrome HGNC:6091 Homo sapiens (human) 3643 INSR inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:6091 Homo sapiens (human) 3643 INSR direct assay evidence used in manual assertion
  • PMID:18972094
DOID:0070220 familial hyperinsulinemic hypoglycemia 5 HGNC:6091 Homo sapiens (human) 3643 INSR inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1168 familial hyperlipidemia HGNC:609 Homo sapiens (human) 344 APOC2 inference by association of genotype from phenotype used in manual assertion
  • PMID:1782747
DOID:0111418 familial apolipoprotein C-II deficiency HGNC:609 Homo sapiens (human) 344 APOC2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2377 multiple sclerosis HGNC:609 Homo sapiens (human) 344 APOC2 inference by association of genotype from phenotype used in manual assertion
  • PMID:10335523
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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: April 7, 2025