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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:9074 systemic lupus erythematosus HGNC:5331 Homo sapiens (human) 64127 NOD2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16642031
DOID:2841 asthma HGNC:17020 Homo sapiens (human) 11213 IRAK3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9821 choroideremia HGNC:1940 Homo sapiens (human) 1121 CHM inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112377 muscular dystrophy-dystroglycanopathy type B14 HGNC:22932 Homo sapiens (human) 29925 GMPPB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3969 papillary thyroid carcinoma HGNC:11825 Homo sapiens (human) 7080 NKX2-1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11870 Pick's disease HGNC:6846 Homo sapiens (human) 5608 MAP2K6 direct assay evidence used in manual assertion
  • PMID:12392790
DOID:0080464 developmental and epileptic encephalopathy 53 HGNC:11503 Homo sapiens (human) 8867 SYNJ1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:5233 Homo sapiens (human) 3304 HSPA1B inference by association of genotype from phenotype used in manual assertion
  • PMID:15223990
DOID:13774 Addison's disease HGNC:7067 Homo sapiens (human) 4261 CIITA inference by association of genotype from phenotype used in manual assertion
  • PMID:18593762
DOID:0090109 autosomal dominant hypocalcemia HGNC:1514 Homo sapiens (human) 846 CASR inference by association of genotype from phenotype used in manual assertion
  • PMID:20501971
  • PMID:7874174
  • PMID:8813042
DOID:0060448 Fleck corneal dystrophy HGNC:23785 Homo sapiens (human) 200576 PIKFYVE inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060025 immunoglobulin alpha deficiency HGNC:5351 Homo sapiens (human) 29851 ICOS inference by association of genotype from phenotype used in manual assertion
  • PMID:19020530
DOID:684 hepatocellular carcinoma HGNC:6190 Homo sapiens (human) 3716 JAK1 inference by association of genotype from phenotype used in manual assertion
  • PMID:23788652
DOID:399 tuberculosis HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B inference by association of genotype from phenotype used in manual assertion
  • PMID:20007930
DOID:7693 abdominal aortic aneurysm HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:10848855
DOID:3908 lung non-small cell carcinoma HGNC:12766 Homo sapiens (human) 7468 NSD2 genetic interaction evidence used in manual assertion
  • PMID:34551195
DOID:0050453 lissencephaly HGNC:20766 Homo sapiens (human) 7846 TUBA1A inference by association of genotype from phenotype used in manual assertion
  • PMID:17584854
DOID:0110515 autosomal recessive nonsyndromic deafness 63 HGNC:25033 Homo sapiens (human) 220074 LRTOMT inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050855 renal fibrosis HGNC:7155 Homo sapiens (human) 4312 MMP1 mutant phenotype evidence used in manual assertion
  • PMID:14674437
DOID:0060931 developmental dysplasia of the hip 1 HGNC:4220 Homo sapiens (human) 8200 GDF5 inference by association of genotype from phenotype used in manual assertion
  • PMID:18947434
DOID:0110390 retinitis pigmentosa 1 HGNC:10263 Homo sapiens (human) 6101 RP1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060549 Barber-Say syndrome HGNC:20670 Homo sapiens (human) 117581 TWIST2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9744 type 1 diabetes mellitus HGNC:13918 Homo sapiens (human) 7916 PRRC2A inference by association of genotype from phenotype used in manual assertion
  • PMID:10987645
  • PMID:15842729
DOID:2732 Rothmund-Thomson syndrome HGNC:9949 Homo sapiens (human) 9401 RECQL4 inference by association of genotype from phenotype used in manual assertion
  • PMID:10678659
  • RGD:7240710
DOID:1485 cystic fibrosis HGNC:7876 Homo sapiens (human) 4846 NOS3 inference by association of genotype from phenotype used in manual assertion
  • PMID:12406848
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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