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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 July 29, 2024
Displaying entries 4826 - 4850 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence Code Names References
DOID:557 kidney disease HGNC:6344 Homo sapiens (human) 9365 KL
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:9922 Homo sapiens (human) 5950 RBP4
  • PMID:25142320
DOID:684 hepatocellular carcinoma FB:FBgn0026597 Drosophila melanogaster (fruit fly) 43565 Axn
  • MGI:6194238
DOID:14227 azoospermia Xenbase:XB-GENE-943997 Xenopus tropicalis (tropical clawed frog) 100217321 ndst2
  • MGI:6194238
DOID:1793 pancreatic cancer HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:19671868
DOID:9452 steatotic liver disease HGNC:16940 Homo sapiens (human) 84649 DGAT2
  • MGI:6194238
DOID:8725 vascular dementia RGD:70982 Rattus norvegicus (Norway rat) 84027 Gsk3b
  • PMID:27118553
DOID:11054 urinary bladder cancer RGD:3130 Rattus norvegicus (Norway rat) 24577 Myc
  • MGI:6194238
DOID:4852 pleomorphic xanthoastrocytoma HGNC:1097 Homo sapiens (human) 673 BRAF
  • PMID:25346165
DOID:0111240 congenital muscular dystrophy-dystroglycanopathy type A2 SGD:S000003431 Saccharomyces cerevisiae S288C 853113 PMT6
  • MGI:6194238
DOID:2986 IgA glomerulonephritis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:12220450
DOID:3770 pulmonary fibrosis HGNC:10798 Homo sapiens (human) 653509 SFTPA1
  • PMID:10543276
  • PMID:13680361
  • PMID:19347046
DOID:14550 root resorption RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • PMID:22372265
DOID:0080322 polycystic kidney disease Xenbase:XB-GENE-17336997 Xenopus laevis (African clawed frog) 380326 alg5.L
  • MGI:6194238
DOID:0110219 Brugada syndrome 2 Xenbase:XB-GENE-969908 Xenopus laevis (African clawed frog) 379962 gpd1l.L
  • MGI:6194238
DOID:11396 pulmonary edema HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:9628235
DOID:3393 coronary artery disease MGI:1929865 Mus musculus (house mouse) 59027 Nampt
  • MGI:6194238
DOID:0090101 lethal congenital glycogen storage disease of heart MGI:1336153 Mus musculus (house mouse) 108099 Prkag2
  • MGI:6194238
DOID:114 heart disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:10763 hypertension FB:FBgn0013763 Drosophila melanogaster (fruit fly) 36868 Idgf6
  • MGI:6194238
DOID:2747 glycogen storage disease HGNC:4699 Homo sapiens (human) 2992 GYG1
  • RGD:7240710
DOID:162 cancer HGNC:8896 Homo sapiens (human) 5230 PGK1
  • MGI:6194238
DOID:9268 glycine encephalopathy HGNC:4208 Homo sapiens (human) 2653 GCSH
  • MGI:6194238
DOID:0080552 congenital disorder of glycosylation Ia HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:19207313
DOID:11832 visual epilepsy FB:FBgn0032729 Drosophila melanogaster (fruit fly) 35156 L2HGDH
  • MGI:6194238

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: August 19, 2024