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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 5876 - 5900 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▼ References
DOID:1727 retinal vein occlusion HGNC:6137 Homo sapiens (human) 3673 ITGA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:12928694
DOID:10887 lepromatous leprosy HGNC:6922 Homo sapiens (human) 4153 MBL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:20650301
DOID:3407 carotid artery disease HGNC:9445 Homo sapiens (human) 5617 PRL inference by association of genotype from phenotype used in manual assertion
  • PMID:17626900
DOID:1324 lung cancer HGNC:9177 Homo sapiens (human) 5426 POLE inference by association of genotype from phenotype used in manual assertion
  • PMID:17855454
DOID:12858 Huntington's disease HGNC:4580 Homo sapiens (human) 2898 GRIK2 inference by association of genotype from phenotype used in manual assertion
  • PMID:10522893
DOID:0111576 dehydrated hereditary stomatocytosis 1 HGNC:28993 Homo sapiens (human) 9780 PIEZO1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:6107 Homo sapiens (human) 3651 PDX1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10545531
  • RGD:7240710
DOID:9744 type 1 diabetes mellitus HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:19127455
  • RGD:7240710
DOID:0110647 long QT syndrome 5 HGNC:6240 Homo sapiens (human) 3753 KCNE1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111091 Fanconi anemia complementation group I HGNC:25568 Homo sapiens (human) 55215 FANCI inference by association of genotype from phenotype used in manual assertion
  • PMID:17452773
  • RGD:7240710
DOID:8670 eating disorder HGNC:14063 Homo sapiens (human) 9759 HDAC4 inference by association of genotype from phenotype used in manual assertion
  • PMID:24216484
DOID:10595 Charcot-Marie-Tooth disease HGNC:10914 Homo sapiens (human) 9990 SLC12A6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8689 anorexia nervosa HGNC:376 Homo sapiens (human) 9472 AKAP6 inference by association of genotype from phenotype used in manual assertion
  • PMID:21079607
DOID:4780 anti-basement membrane glomerulonephritis HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21569485
DOID:648 kuru HGNC:9449 Homo sapiens (human) 5621 PRNP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112133 severe congenital neutropenia 3 HGNC:16915 Homo sapiens (human) 10456 HAX1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10534 stomach cancer HGNC:9644 Homo sapiens (human) 5781 PTPN11 inference by association of genotype from phenotype used in manual assertion
  • PMID:27614952
DOID:2559 opiate dependence HGNC:24154 Homo sapiens (human) 168667 BMPER inference by association of genotype from phenotype used in manual assertion
  • PMID:18438686
DOID:9970 obesity HGNC:8743 Homo sapiens (human) 5122 PCSK1 inference by association of genotype from phenotype used in manual assertion
  • PMID:9207799
DOID:0050861 colorectal adenocarcinoma HGNC:3527 Homo sapiens (human) 2146 EZH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21926398
DOID:12849 autistic disorder HGNC:8978 Homo sapiens (human) 5294 PIK3CG inference by association of genotype from phenotype used in manual assertion
  • PMID:14627686
DOID:0112166 autosomal dominant nonsyndromic deafness 75 HGNC:12347 Homo sapiens (human) 8295 TRRAP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11054 urinary bladder cancer HGNC:7553 Homo sapiens (human) 4609 MYC inference by association of genotype from phenotype used in manual assertion
  • PMID:23284801
DOID:0060681 autosomal dominant nocturnal frontal lobe epilepsy HGNC:1962 Homo sapiens (human) 1141 CHRNB2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11104662
DOID:0112361 spondylocostal dysostosis 3 HGNC:6560 Homo sapiens (human) 3955 LFNG inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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International Collaboration

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