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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 12101 - 12125 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References ▲
DOID:0081272 Sandestig-Stefanova syndrome HGNC:17859 Homo sapiens (human) 23511 NUP188 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050956 spinocerebellar ataxia type 6 HGNC:1388 Homo sapiens (human) 773 CACNA1A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080264 exudative vitreoretinopathy 7 HGNC:2514 Homo sapiens (human) 1499 CTNNB1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070272 hereditary nonpolyposis colorectal cancer type 5 HGNC:7329 Homo sapiens (human) 2956 MSH6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12365 malaria HGNC:1663 Homo sapiens (human) 948 CD36 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050813 spondyloepiphyseal dysplasia with congenital joint dislocations HGNC:1971 Homo sapiens (human) 9469 CHST3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070356 visual impairment and progressive phthisis bulbi HGNC:6897 Homo sapiens (human) 4140 MARK3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080093 myofibrillar myopathy 2 HGNC:2389 Homo sapiens (human) 1410 CRYAB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111955 immunodeficiency 27A HGNC:5439 Homo sapiens (human) 3459 IFNGR1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080554 congenital disorder of glycosylation Ib HGNC:7216 Homo sapiens (human) 4351 MPI inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0090101 lethal congenital glycogen storage disease of heart HGNC:9386 Homo sapiens (human) 51422 PRKAG2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060428 SATB2-associated syndrome HGNC:21637 Homo sapiens (human) 23314 SATB2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0081327 neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures HGNC:14282 Homo sapiens (human) 64207 IRF2BPL inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110217 Leber congenital amaurosis 17 HGNC:4221 Homo sapiens (human) 392255 GDF6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110327 hypertrophic cardiomyopathy 26 HGNC:3756 Homo sapiens (human) 2318 FLNC inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112137 combined oxidative phosphorylation deficiency 51 HGNC:24717 Homo sapiens (human) 55037 PTCD3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110509 autosomal recessive nonsyndromic deafness 53 HGNC:2187 Homo sapiens (human) 1302 COL11A2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111735 X-linked deafness 4 HGNC:11122 Homo sapiens (human) 23676 SMPX inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080930 primary localized cutaneous amyloidosis 1 HGNC:8507 Homo sapiens (human) 9180 OSMR inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9119 acute myeloid leukemia HGNC:11730 Homo sapiens (human) 7015 TERT inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080286 spinocerebellar ataxia 44 HGNC:4593 Homo sapiens (human) 2911 GRM1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1485 cystic fibrosis HGNC:3616 Homo sapiens (human) 2212 FCGR2A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2513 basal cell carcinoma HGNC:9585 Homo sapiens (human) 5727 PTCH1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0081235 autosomal recessive intellectual developmental disorder 76 HGNC:4571 Homo sapiens (human) 2890 GRIA1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050545 visceral heterotaxy HGNC:14357 Homo sapiens (human) 118856 MMP21 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