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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 10126 - 10150 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence References
DOID:9256 colorectal cancer HGNC:8977 Homo sapiens (human) 5293 PIK3CD direct assay evidence used in manual assertion
  • PMID:25366420
DOID:0111936 immunodeficiency 14 HGNC:8977 Homo sapiens (human) 5293 PIK3CD inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:5419 schizophrenia HGNC:8977 Homo sapiens (human) 5293 PIK3CD inference by association of genotype from phenotype used in manual assertion
  • PMID:22689948
DOID:1380 endometrial cancer HGNC:8977 Homo sapiens (human) 5293 PIK3CD genetic interaction evidence used in manual assertion
  • PMID:21478295
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:0050211 swine influenza HGNC:8978 Homo sapiens (human) 5294 PIK3CG inference by association of genotype from phenotype used in manual assertion
  • PMID:29867955
DOID:612 primary immunodeficiency disease HGNC:8978 Homo sapiens (human) 5294 PIK3CG inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:234 colon adenocarcinoma HGNC:8981 Homo sapiens (human) 8503 PIK3R3 direct assay evidence used in manual assertion
  • PMID:24632606
DOID:0060448 Fleck corneal dystrophy HGNC:23785 Homo sapiens (human) 200576 PIKFYVE inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060369 Parkinson's disease 6 HGNC:14581 Homo sapiens (human) 65018 PINK1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:14581 Homo sapiens (human) 65018 PINK1 inference by association of genotype from phenotype used in manual assertion
  • PMID:25639775
  • PMID:26223426
DOID:684 hepatocellular carcinoma HGNC:30046 Homo sapiens (human) 54984 PINX1 inference by association of genotype from phenotype used in manual assertion
  • PMID:27221889
DOID:0060653 lethal congenital contracture syndrome 3 HGNC:8996 Homo sapiens (human) 23396 PIP5K1C inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111010 cone-rod dystrophy 5 HGNC:21043 Homo sapiens (human) 83394 PITPNM3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070411 autosomal recessive spinocerebellar ataxia 30 HGNC:17663 Homo sapiens (human) 10531 PITRM1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11836 clubfoot HGNC:9004 Homo sapiens (human) 5307 PITX1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050647 Arts syndrome HGNC:9005 Homo sapiens (human) 5308 PITX2 inference by association of genotype from phenotype used in manual assertion
  • PMID:17701896
DOID:0111548 ring dermoid of cornea HGNC:9005 Homo sapiens (human) 5308 PITX2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:14686 Axenfeld-Rieger syndrome HGNC:9005 Homo sapiens (human) 5308 PITX2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16876867
  • PMID:19052653
DOID:0080609 anterior segment dysgenesis 4 HGNC:9005 Homo sapiens (human) 5308 PITX2 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:9970 obesity FB:FBgn0038201 Drosophila melanogaster (fruit fly) 41713 PK1-R combinatorial experimental and author inference evidence used in manual assertion
  • PMID:25651184
DOID:0110858 polycystic kidney disease 1 HGNC:9008 Homo sapiens (human) 5310 PKD1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10941 intracranial aneurysm HGNC:9008 Homo sapiens (human) 5310 PKD1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12842373
DOID:898 autosomal dominant polycystic kidney disease HGNC:9008 Homo sapiens (human) 5310 PKD1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21115670
  • PMID:8554072
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: April 7, 2025