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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 651 - 675 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:13544 low tension glaucoma HGNC:7610 Homo sapiens (human) 4653 MYOC inference by association of genotype from phenotype used in manual assertion
  • PMID:16148883
DOID:5339 cyclic hematopoiesis HGNC:3309 Homo sapiens (human) 1991 ELANE inference by association of genotype from phenotype used in manual assertion
  • PMID:21425445
  • RGD:7240710
DOID:6432 pulmonary hypertension RGD:3811 Rattus norvegicus (Norway rat) 24807 Tacr1 mutant phenotype evidence used in manual assertion
  • PMID:12662901
DOID:0080634 nanophthalmos HGNC:18121 Homo sapiens (human) 83552 MFRP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11335 sarcoidosis HGNC:2097 Homo sapiens (human) 1215 CMA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16446531
DOID:0050127 sinusitis HGNC:6709 Homo sapiens (human) 4049 LTA inference by association of genotype from phenotype used in manual assertion
  • PMID:11037831
DOID:219 colon cancer SGD:S000000671 Saccharomyces cerevisiae S288C 850438 ERS1 sequence similarity evidence used in manual assertion
  • PMID:25860149
DOID:12858 Huntington's disease HGNC:14929 Homo sapiens (human) 23411 SIRT1 inference by association of genotype from phenotype used in manual assertion
  • PMID:9949199
DOID:5212 congenital disorder of glycosylation SGD:S000000314 Saccharomyces cerevisiae S288C 852407 ALG1 genetic interaction evidence used in manual assertion
  • PMID:24157261
DOID:9478 postpartum depression MGI:95622 Mus musculus (house mouse) 14403 Gabrd author statement supported by traceable reference
  • PMID:18667149
DOID:9649 congenital nystagmus HGNC:10249 Homo sapiens (human) 6091 ROBO1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10003 sensorineural hearing loss HGNC:11720 Homo sapiens (human) 7007 TECTA inference by association of genotype from phenotype used in manual assertion
  • PMID:9590290
  • PMID:9949200
DOID:9952 acute lymphoblastic leukemia HGNC:11730 Homo sapiens (human) 7015 TERT inference by association of genotype from phenotype used in manual assertion
  • PMID:23066086
DOID:0080925 cytochrome P450 oxidoreductase deficiency HGNC:9208 Homo sapiens (human) 5447 POR inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:678 progressive supranuclear palsy HGNC:6893 Homo sapiens (human) 4137 MAPT inference by association of genotype from phenotype used in manual assertion
  • PMID:15792962
  • PMID:16839689
  • PMID:19879020
DOID:0081360 spastic quadriplegic cerebral palsy 2 HGNC:19309 Homo sapiens (human) 23189 KANK1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110255 cataract 5 multiple types HGNC:5227 Homo sapiens (human) 3299 HSF4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1574 alcohol use disorder HGNC:5302 Homo sapiens (human) 3363 HTR7 inference by association of genotype from phenotype used in manual assertion
  • PMID:21184583
DOID:3070 high grade glioma HGNC:9588 Homo sapiens (human) 5728 PTEN inference by association of genotype from phenotype used in manual assertion
  • PMID:9090379
  • RGD:7240710
DOID:8577 ulcerative colitis HGNC:2602 Homo sapiens (human) 1591 CYP24A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:28811712
DOID:13533 osteopetrosis HGNC:29017 Homo sapiens (human) 9842 PLEKHM1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050908 myelodysplastic syndrome HGNC:4171 Homo sapiens (human) 2624 GATA2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1580 diffuse scleroderma HGNC:3616 Homo sapiens (human) 2212 FCGR2A direct assay evidence used in manual assertion
  • PMID:8254199
DOID:5844 myocardial infarction HGNC:11766 Homo sapiens (human) 7040 TGFB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16543493
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:6554 Homo sapiens (human) 3953 LEPR inference by association of genotype from phenotype used in manual assertion
  • PMID:23278404
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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