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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 13476 - 13500 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References ▲
DOID:0080030 spondyloepimetaphyseal dysplasia, Missouri type HGNC:7159 Homo sapiens (human) 4322 MMP13 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110808 hereditary spastic paraplegia 56 HGNC:20582 Homo sapiens (human) 113612 CYP2U1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080486 peroxisome biogenesis disorder 12A HGNC:9713 Homo sapiens (human) 5824 PEX19 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050989 episodic ataxia type 1 HGNC:6218 Homo sapiens (human) 3736 KCNA1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110120 Axenfeld-Rieger syndrome type 1 HGNC:9005 Homo sapiens (human) 5308 PITX2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:13543 hyperparathyroidism HGNC:16783 Homo sapiens (human) 79577 CDC73 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110883 inflammatory bowel disease 17 HGNC:19100 Homo sapiens (human) 149233 IL23R inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111905 autosomal recessive thrombophilia due to protein S deficiency HGNC:9456 Homo sapiens (human) 5627 PROS1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080141 mosaic variegated aneuploidy syndrome 1 HGNC:1149 Homo sapiens (human) 701 BUB1B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2394 ovarian cancer HGNC:8975 Homo sapiens (human) 5290 PIK3CA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:4586 familial meningioma HGNC:11109 Homo sapiens (human) 6605 SMARCE1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111402 mucopolysaccharidosis type IIID HGNC:4422 Homo sapiens (human) 2799 GNS inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111853 primary ciliary dyskinesia 40 HGNC:2953 Homo sapiens (human) 1770 DNAH9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110446 dilated cardiomyopathy 1W HGNC:12665 Homo sapiens (human) 7414 VCL inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060610 megacystis-microcolon-intestinal hypoperistalsis syndrome HGNC:7590 Homo sapiens (human) 4638 MYLK inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9970 obesity HGNC:10660 Homo sapiens (human) 9672 SDC3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111932 severe congenital encephalopathy due to MECP2 mutation HGNC:6990 Homo sapiens (human) 4204 MECP2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070210 hereditary lymphedema IA HGNC:3767 Homo sapiens (human) 2324 FLT4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110263 cataract 19 multiple types HGNC:6610 Homo sapiens (human) 3982 LIM2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110786 hereditary spastic paraplegia 35 HGNC:21197 Homo sapiens (human) 79152 FA2H inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070221 progressive familial intrahepatic cholestasis HGNC:29955 Homo sapiens (human) 200931 SLC51A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110662 congenital myasthenic syndrome 1B HGNC:1955 Homo sapiens (human) 1134 CHRNA1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070269 congenital disorder of glycosylation type IIq HGNC:6546 Homo sapiens (human) 22796 COG2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070491 mitochondrial complex IV deficiency nuclear type 1 HGNC:11474 Homo sapiens (human) 6834 SURF1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080135 multiple mitochondrial dysfunctions syndrome 3 HGNC:27302 Homo sapiens (human) 200205 IBA57 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