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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 2701 - 2725 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:1793 pancreatic cancer HGNC:7371 Homo sapiens (human) 10232 MSLN direct assay evidence used in manual assertion
  • PMID:17785569
  • PMID:19843662
DOID:11335 sarcoidosis HGNC:2707 Homo sapiens (human) 1636 ACE inference by association of genotype from phenotype used in manual assertion
  • PMID:11168787
  • PMID:18496980
  • PMID:29229112
DOID:0090127 camptodactyly-arthropathy-coxa vara-pericarditis syndrome HGNC:9364 Homo sapiens (human) 10216 PRG4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1059 intellectual disability WB:WBGene00003182 Caenorhabditis elegans 172732 mef-2 mutant phenotype evidence used in manual assertion
  • PMID:22859820
DOID:9452 steatotic liver disease HGNC:286 Homo sapiens (human) 154 ADRB2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11718682
DOID:4079 heart valve disease MGI:894693 Mus musculus (house mouse) 14423 Galnt1 author statement supported by traceable reference
  • PMID:25615642
DOID:0050338 primary bacterial infectious disease FB:FBgn0003444 Drosophila melanogaster (fruit fly) 33196 smo combinatorial experimental and author inference evidence used in manual assertion
  • PMID:25639794
DOID:9562 primary ciliary dyskinesia MGI:1315205 Mus musculus (house mouse) 20563 Slit2 author statement supported by traceable reference
  • MGI:5284969
DOID:9256 colorectal cancer HGNC:8977 Homo sapiens (human) 5293 PIK3CD direct assay evidence used in manual assertion
  • PMID:25366420
DOID:9074 systemic lupus erythematosus HGNC:15633 Homo sapiens (human) 54106 TLR9 inference by association of genotype from phenotype used in manual assertion
  • PMID:19130296
DOID:653 purine-pyrimidine metabolic disorder HGNC:7892 Homo sapiens (human) 4860 PNP inference by association of genotype from phenotype used in manual assertion
  • PMID:3029074
DOID:653 purine-pyrimidine metabolic disorder HGNC:794 Homo sapiens (human) 471 ATIC inference by association of genotype from phenotype used in manual assertion
  • PMID:15114530
DOID:0080576 spondyloepimetaphyseal dysplasia, Genevieve-type HGNC:19237 Homo sapiens (human) 54187 NANS inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3209 junctional epidermolysis bullosa MGI:88450 Mus musculus (house mouse) 12821 Col17a1 author statement supported by traceable reference
  • PMID:37796769
DOID:0112319 Kanzaki disease HGNC:7631 Homo sapiens (human) 4668 NAGA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10763 hypertension HGNC:2213 Homo sapiens (human) 1293 COL6A3 inference by association of genotype from phenotype used in manual assertion
  • PMID:30226566
DOID:5082 liver cirrhosis HGNC:19964 Homo sapiens (human) 22846 VASH1 direct assay evidence used in manual assertion
  • PMID:24390792
DOID:0080600 COVID-19 HGNC:4932 Homo sapiens (human) 3106 HLA-B inference by association of genotype from phenotype used in manual assertion
  • PMID:32424945
DOID:0050477 Liddle syndrome MGI:104696 Mus musculus (house mouse) 20277 Scnn1b author statement supported by traceable reference
  • PMID:10589691
DOID:0050689 brachydactyly-syndactyly syndrome HGNC:5136 Homo sapiens (human) 3239 HOXD13 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:5082 liver cirrhosis HGNC:11050 Homo sapiens (human) 6532 SLC6A4 inference by association of genotype from phenotype used in manual assertion
  • PMID:11236836
DOID:10923 sickle cell anemia HGNC:603 Homo sapiens (human) 338 APOB direct assay evidence used in manual assertion
  • PMID:24035168
DOID:11612 polycystic ovary syndrome HGNC:3971 Homo sapiens (human) 10468 FST inference by association of genotype from phenotype used in manual assertion
  • PMID:10411917
DOID:0070133 autosomal recessive cutis laxa type IB HGNC:3219 Homo sapiens (human) 30008 EFEMP2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2921 glomerulonephritis RGD:2311 Rattus norvegicus (Norway rat) 25407 Cd59b mutant phenotype evidence used in manual assertion
  • PMID:7523753
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International Collaboration

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: December 8, 2025