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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 13701 - 13725 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▼ Evidence References
DOID:0110052 amelogenesis imperfecta type 1B MGI:1333772 Mus musculus (house mouse) 13801 Enam author statement supported by traceable reference
  • PMID:15649948
  • PMID:24603688
DOID:6419 tetralogy of Fallot HGNC:9644 Homo sapiens (human) 5781 PTPN11 inference by association of genotype from phenotype used in manual assertion
  • PMID:22503907
DOID:9352 type 2 diabetes mellitus HGNC:4498 Homo sapiens (human) 2864 FFAR1 mutant phenotype evidence used in manual assertion
  • PMID:19401434
DOID:0110820 hereditary spastic paraplegia 75 HGNC:6783 Homo sapiens (human) 4099 MAG inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111228 Sveinsson chorioretinal atrophy HGNC:11714 Homo sapiens (human) 7003 TEAD1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050848 obstructive sleep apnea HGNC:7997 Homo sapiens (human) 3084 NRG1 inference by association of genotype from phenotype used in manual assertion
  • PMID:25325441
DOID:2957 pulmonary tuberculosis HGNC:10798 Homo sapiens (human) 653509 SFTPA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12476938
  • PMID:16292672
DOID:0112350 spermatogenic failure 61 HGNC:11356 Homo sapiens (human) 10734 STAG3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:936 brain disease HGNC:13481 Homo sapiens (human) 81622 UNC93B1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2367 neuroaxonal dystrophy HGNC:9039 Homo sapiens (human) 8398 PLA2G6 inference by association of genotype from phenotype used in manual assertion
  • PMID:17033970
  • PMID:19138334
DOID:1588 thrombocytopenia HGNC:6138 Homo sapiens (human) 3674 ITGA2B inference by association of genotype from phenotype used in manual assertion
  • PMID:21454453
DOID:0081020 congenital fibrosis of the extraocular muscles 5 HGNC:18603 Homo sapiens (human) 84570 COL25A1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3343 glycoproteinosis HGNC:23026 Homo sapiens (human) 84572 GNPTG inference by association of genotype from phenotype used in manual assertion
  • PMID:10712439
DOID:4947 cholangiocarcinoma HGNC:7646 Homo sapiens (human) 10 NAT2 inference by association of genotype from phenotype used in manual assertion
  • PMID:15901993
DOID:0050559 Fukuyama congenital muscular dystrophy HGNC:3622 Homo sapiens (human) 2218 FKTN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10923 sickle cell anemia MGI:98385 Mus musculus (house mouse) 20739 Spta1 author statement supported by traceable reference
  • PMID:8355480
DOID:1584 acute chest syndrome HGNC:4827 Homo sapiens (human) 3043 HBB inference by association of genotype from phenotype used in manual assertion
  • PMID:23952145
DOID:3908 lung non-small cell carcinoma HGNC:25941 Homo sapiens (human) 54790 TET2 inference by association of genotype from phenotype used in manual assertion
  • PMID:32554069
DOID:13608 biliary atresia HGNC:11255 Homo sapiens (human) 6696 SPP1 direct assay evidence used in manual assertion
  • PMID:15845635
DOID:0111784 otopalatodigital syndrome type 2 HGNC:3754 Homo sapiens (human) 2316 FLNA inference by association of genotype from phenotype used in manual assertion
  • PMID:12612583
  • RGD:7240710
DOID:9952 acute lymphoblastic leukemia HGNC:959 Homo sapiens (human) 581 BAX inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:4441 dysgerminoma HGNC:6342 Homo sapiens (human) 3815 KIT inference by association of genotype from phenotype used in manual assertion
  • PMID:10362788
DOID:0080072 intestinal pseudo-obstruction MGI:1916732 Mus musculus (house mouse) 69482 Nup35 author statement supported by traceable reference
  • PMID:27427419
DOID:0110274 autosomal recessive limb-girdle muscular dystrophy HGNC:19743 Homo sapiens (human) 29954 POMT2 inference by association of genotype from phenotype used in manual assertion
  • PMID:17923109
DOID:0081030 central conducting lymphatic anomaly HGNC:3395 Homo sapiens (human) 2050 EPHB4 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