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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 13426 - 13450 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:9744 type 1 diabetes mellitus HGNC:1603 Homo sapiens (human) 729230 CCR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:10400139
DOID:0070048 GAND syndrome HGNC:30778 Homo sapiens (human) 57459 GATAD2B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:5082 liver cirrhosis HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11336748
DOID:0080664 diaphyseal medullary stenosis with malignant fibrous histiocytoma HGNC:7413 Homo sapiens (human) 4507 MTAP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0081343 congenital myopathy 9A HGNC:4023 Homo sapiens (human) 8087 FXR1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050458 juvenile myelomonocytic leukemia MGI:97306 Mus musculus (house mouse) 18015 Nf1 author statement supported by traceable reference
  • PMID:14982883
DOID:0050580 hereditary lymphedema HGNC:485 Homo sapiens (human) 285 ANGPT2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111800 syndromic microphthalmia 12 HGNC:9865 Homo sapiens (human) 5915 RARB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0090053 episodic kinesigenic dyskinesia 1 MGI:1916267 Mus musculus (house mouse) 69017 Prrt2 author statement supported by traceable reference
  • PMID:32891704
DOID:9255 frontotemporal dementia HGNC:6893 Homo sapiens (human) 4137 MAPT mutant phenotype evidence used in manual assertion
  • PMID:16407562
DOID:3312 bipolar disorder HGNC:17089 Homo sapiens (human) 23345 SYNE1 inference by association of genotype from phenotype used in manual assertion
  • PMID:28178086
DOID:1612 breast cancer HGNC:9956 Homo sapiens (human) 5971 RELB direct assay evidence used in manual assertion
  • PMID:9724088
DOID:0080572 congenital disorder of glycosylation Iw SGD:S000002990 Saccharomyces cerevisiae S288C 852862 STT3 sequence similarity evidence used in manual assertion
  • PMID:34653363
DOID:10286 prostate carcinoma HGNC:9393 Homo sapiens (human) 5578 PRKCA mutant phenotype evidence used in manual assertion
  • PMID:9474241
DOID:0070004 myeloid neoplasm HGNC:1541 Homo sapiens (human) 867 CBL inference by association of genotype from phenotype used in manual assertion
  • PMID:19387008
  • PMID:22315494
DOID:3526 cerebral infarction HGNC:4931 Homo sapiens (human) 3105 HLA-A inference by association of genotype from phenotype used in manual assertion
  • PMID:24767290
DOID:0080693 Noonan syndrome-like disorder with loose anagen hair 2 HGNC:9282 Homo sapiens (human) 5500 PPP1CB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:13001 carotid stenosis HGNC:7155 Homo sapiens (human) 4312 MMP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12364729
DOID:1849 cannabis dependence HGNC:108 Homo sapiens (human) 43 ACHE inference by association of genotype from phenotype used in manual assertion
  • PMID:31129131
DOID:1148 polydactyly HGNC:10848 Homo sapiens (human) 6469 SHH inference by association of genotype from phenotype used in manual assertion
  • PMID:22903933
DOID:0060108 brain glioma HGNC:9665 Homo sapiens (human) 5787 PTPRB mutant phenotype evidence used in manual assertion
  • PMID:16923162
DOID:1826 epilepsy RGD:628742 Rattus norvegicus (Norway rat) 252892 Lgi1 mutant phenotype evidence used in manual assertion
  • PMID:22589250
DOID:5844 myocardial infarction HGNC:3531 Homo sapiens (human) 2162 F13A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12480694
  • RGD:7240710
DOID:0111947 immunodeficiency 21 HGNC:4171 Homo sapiens (human) 2624 GATA2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111461 cardiofaciocutaneous syndrome 2 HGNC:6407 Homo sapiens (human) 3845 KRAS 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: December 8, 2025