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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 13451 - 13475 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References ▲
DOID:0080410 familial adenomatous polyposis 2 HGNC:7527 Homo sapiens (human) 4595 MUTYH inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080107 microcephaly and chorioretinopathy 3 HGNC:16691 Homo sapiens (human) 27229 TUBGCP4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111998 immunodeficiency 66 HGNC:14334 Homo sapiens (human) 57591 MRTFA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111028 hemochromatosis type 4 HGNC:10909 Homo sapiens (human) 30061 SLC40A1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111070 congenital bile acid synthesis defect 3 HGNC:2652 Homo sapiens (human) 9420 CYP7B1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080746 Sweet syndrome HGNC:6998 Homo sapiens (human) 4210 MEFV inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:7400 Nijmegen breakage syndrome HGNC:7652 Homo sapiens (human) 4683 NBN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080564 congenital disorder of glycosylation Il HGNC:15672 Homo sapiens (human) 79796 ALG9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110632 megaconial type congenital muscular dystrophy HGNC:1938 Homo sapiens (human) 1120 CHKB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110810 hereditary spastic paraplegia 5A HGNC:2652 Homo sapiens (human) 9420 CYP7B1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3070 high grade glioma HGNC:5382 Homo sapiens (human) 3417 IDH1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060302 type II complement component 8 deficiency HGNC:1353 Homo sapiens (human) 732 C8B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:612 primary immunodeficiency disease HGNC:9666 Homo sapiens (human) 5788 PTPRC inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080471 developmental and epileptic encephalopathy 92 HGNC:4082 Homo sapiens (human) 2561 GABRB2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060537 mitochondrial complex II deficiency HGNC:10680 Homo sapiens (human) 6389 SDHA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070051 autosomal dominant intellectual developmental disorder 21 HGNC:13723 Homo sapiens (human) 10664 CTCF inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:4051 alveolar rhabdomyosarcoma HGNC:3819 Homo sapiens (human) 2308 FOXO1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111254 glutaric acidemia I HGNC:4189 Homo sapiens (human) 2639 GCDH inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112209 developmental and epileptic encephalopathy 73 HGNC:10057 Homo sapiens (human) 11342 RNF13 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0081426 autosomal recessive distal hereditary motor neuronopathy 7 HGNC:30910 Homo sapiens (human) 64856 VWA1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060970 Cornelia de Lange syndrome 6 HGNC:13575 Homo sapiens (human) 23476 BRD4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3526 cerebral infarction HGNC:3542 Homo sapiens (human) 2153 F5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111943 immunodeficiency 48 HGNC:12858 Homo sapiens (human) 7535 ZAP70 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:14004 thoracic aortic aneurysm HGNC:6664 Homo sapiens (human) 4015 LOX inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111583 carboxypeptidase N deficiency HGNC:2312 Homo sapiens (human) 1369 CPN1 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