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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 14226 - 14250 of 14279 in total
Disease ID Disease Name ▲ Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:12306 vitiligo HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16409268
DOID:12306 vitiligo HGNC:11180 Homo sapiens (human) 6648 SOD2 inference by association of genotype from phenotype used in manual assertion
  • PMID:24036105
DOID:12306 vitiligo HGNC:5232 Homo sapiens (human) 3303 HSPA1A mutant phenotype evidence used in manual assertion
  • PMID:23447019
DOID:12306 vitiligo HGNC:4893 Homo sapiens (human) 3082 HGF mutant phenotype evidence used in manual assertion
  • PMID:16117796
DOID:12306 vitiligo HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16420246
  • PMID:9653015
DOID:12306 vitiligo HGNC:3467 Homo sapiens (human) 2099 ESR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15381239
DOID:12306 vitiligo HGNC:11848 Homo sapiens (human) 7097 TLR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:22429552
DOID:12306 vitiligo HGNC:5438 Homo sapiens (human) 3458 IFNG inference by association of genotype from phenotype used in manual assertion
  • PMID:23777204
DOID:12306 vitiligo HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16420246
  • PMID:9653015
DOID:14175 von Hippel-Lindau disease HGNC:7173 Homo sapiens (human) 4314 MMP3 inference by association of genotype from phenotype used in manual assertion
  • PMID:19551141
DOID:12531 von Willebrand's disease HGNC:3541 Homo sapiens (human) 2152 F3 direct assay evidence used in manual assertion
  • PMID:4546024
DOID:12531 von Willebrand's disease HGNC:12726 Homo sapiens (human) 7450 VWF direct assay evidence used in manual assertion
  • PMID:26239086
DOID:12531 von Willebrand's disease MGI:98941 Mus musculus (house mouse) 22371 Vwf author statement supported by traceable reference
  • PMID:30565388
DOID:0060573 von Willebrand's disease 1 HGNC:9051 Homo sapiens (human) 5327 PLAT direct assay evidence used in manual assertion
  • PMID:1419807
DOID:0060573 von Willebrand's disease 1 HGNC:6137 Homo sapiens (human) 3673 ITGA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:15226188
DOID:0060573 von Willebrand's disease 1 HGNC:12726 Homo sapiens (human) 7450 VWF inference by association of genotype from phenotype used in manual assertion
  • PMID:8839833
  • RGD:7240710
DOID:0060573 von Willebrand's disease 1 HGNC:6138 Homo sapiens (human) 3674 ITGA2B inference by association of genotype from phenotype used in manual assertion
  • PMID:15226188
DOID:0060574 von Willebrand's disease 2 HGNC:12726 Homo sapiens (human) 7450 VWF mutant phenotype evidence used in manual assertion
  • PMID:20589313
DOID:0060574 von Willebrand's disease 2 HGNC:6137 Homo sapiens (human) 3673 ITGA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16409463
DOID:0060574 von Willebrand's disease 2 HGNC:12726 Homo sapiens (human) 7450 VWF inference by association of genotype from phenotype used in manual assertion
  • PMID:10959688
  • PMID:26019279
  • PMID:8839848
  • RGD:7240710
DOID:0060574 von Willebrand's disease 2 MGI:98941 Mus musculus (house mouse) 22371 Vwf author statement supported by traceable reference
  • PMID:27212476
DOID:0111054 von Willebrand's disease 3 HGNC:12726 Homo sapiens (human) 7450 VWF inference by association of genotype from phenotype used in manual assertion
  • PMID:7831648
  • RGD:7240710
DOID:1245 vulva cancer HGNC:7876 Homo sapiens (human) 4846 NOS3 inference by association of genotype from phenotype used in manual assertion
  • PMID:15196865
DOID:1245 vulva cancer HGNC:4931 Homo sapiens (human) 3105 HLA-A inference by association of genotype from phenotype used in manual assertion
  • PMID:12543794
DOID:1245 vulva cancer HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12543794
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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