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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:7148 rheumatoid arthritis HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A inference by association of genotype from phenotype used in manual assertion
  • PMID:25311255
DOID:9352 type 2 diabetes mellitus HGNC:11289 Homo sapiens (human) 6720 SREBF1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18692268
DOID:0060708 lymphoproliferative syndrome 2 HGNC:11922 Homo sapiens (human) 939 CD27 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080549 Noonan syndrome with multiple lentigines 2 HGNC:9829 Homo sapiens (human) 5894 RAF1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:3535 Homo sapiens (human) 2147 F2 direct assay evidence used in manual assertion
  • PMID:14961168
DOID:13544 low tension glaucoma MGI:99917 Mus musculus (house mouse) 20512 Slc1a3 author statement supported by traceable reference
  • PMID:17607354
DOID:0080176 meningococcal meningitis HGNC:11850 Homo sapiens (human) 7099 TLR4 inference by association of genotype from phenotype used in manual assertion
  • PMID:23691182
DOID:10584 retinitis pigmentosa HGNC:11179 Homo sapiens (human) 6647 SOD1 mutant phenotype evidence used in manual assertion
  • PMID:19293779
DOID:0110913 adult hypophosphatasia HGNC:438 Homo sapiens (human) 249 ALPL inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2216 factor V deficiency HGNC:6631 Homo sapiens (human) 3998 LMAN1 inference by association of genotype from phenotype used in manual assertion
  • PMID:9546392
DOID:2986 IgA glomerulonephritis HGNC:243 Homo sapiens (human) 118 ADD1 inference by association of genotype from phenotype used in manual assertion
  • PMID:19838659
DOID:874 bacterial pneumonia HGNC:2438 Homo sapiens (human) 1440 CSF3 direct assay evidence used in manual assertion
  • PMID:12352049
DOID:1919 Lesch-Nyhan syndrome FB:FBgn0000109 Drosophila melanogaster (fruit fly) 48224 Aprt combinatorial experimental and author inference evidence used in manual assertion
  • PMID:38700995
DOID:1882 atrial heart septal defect HGNC:11187 Homo sapiens (human) 6654 SOS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17143285
DOID:3910 lung adenocarcinoma HGNC:1455 Homo sapiens (human) 811 CALR mutant phenotype evidence used in manual assertion
  • PMID:18245558
DOID:1749 squamous cell carcinoma HGNC:13861 Homo sapiens (human) 11178 LZTS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10097140
DOID:13375 temporal arteritis HGNC:3327 Homo sapiens (human) 2006 ELN direct assay evidence used in manual assertion
  • PMID:9101501
DOID:12217 Lewy body dementia HGNC:11138 Homo sapiens (human) 6622 SNCA mutant phenotype evidence used in manual assertion
  • PMID:11733371
DOID:10763 hypertension RGD:68407 Rattus norvegicus (Norway rat) 29216 Lrp2 direct assay evidence used in manual assertion
  • PMID:10919857
DOID:9352 type 2 diabetes mellitus HGNC:13633 Homo sapiens (human) 9370 ADIPOQ inference by association of genotype from phenotype used in manual assertion
  • PMID:24655058
DOID:0111057 platelet-type bleeding disorder 11 HGNC:14388 Homo sapiens (human) 51206 GP6 inference by association of genotype from phenotype used in manual assertion
  • PMID:23815599
  • RGD:7240710
DOID:1928 Williams-Beuren syndrome MGI:1277959 Mus musculus (house mouse) 13385 Dlg4 author statement supported by traceable reference
  • PMID:20952458
DOID:0050741 alcohol dependence HGNC:5293 Homo sapiens (human) 3356 HTR2A inference by association of genotype from phenotype used in manual assertion
  • PMID:19060480
  • PMID:21930285
  • PMID:23321485
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:0110079 Leber congenital amaurosis 8 HGNC:2343 Homo sapiens (human) 23418 CRB1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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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