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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 October 9, 2024
Displaying entries 68351 - 68375 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:332 amyotrophic lateral sclerosis HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • PMID:12675919
DOID:8689 anorexia nervosa HGNC:7978 Homo sapiens (human) 2908 NR3C1
  • PMID:10356629
DOID:10652 Alzheimer's disease HGNC:11185 Homo sapiens (human) 6653 SORL1
  • PMID:15313836
DOID:3459 breast carcinoma HGNC:12428 Homo sapiens (human) 7291 TWIST1
  • PMID:27524420
DOID:2841 asthma HGNC:9451 Homo sapiens (human) 5624 PROC
  • PMID:26381519
DOID:1875 impotence RGD:2081 Rattus norvegicus (Norway rat) 24185 Akt1
  • PMID:21235725
DOID:12858 Huntington's disease RGD:1310309 Rattus norvegicus (Norway rat) 293504 Qprt
  • PMID:2527078
DOID:10286 prostate carcinoma HGNC:910 Homo sapiens (human) 563 AZGP1
  • PMID:11309332
DOID:11446 sciatic neuropathy HGNC:4893 Homo sapiens (human) 3082 HGF
  • PMID:18941443
DOID:341 peripheral vascular disease HGNC:6018 Homo sapiens (human) 3569 IL6
  • PMID:19397692
DOID:11119 Gilles de la Tourette syndrome HGNC:16882 Homo sapiens (human) 10021 HCN4
  • PMID:22683190
DOID:8719 in situ carcinoma HGNC:10473 Homo sapiens (human) 864 RUNX3
  • PMID:19763613
DOID:3910 lung adenocarcinoma HGNC:7553 Homo sapiens (human) 4609 MYC
  • PMID:20033209
DOID:3068 glioblastoma HGNC:9884 Homo sapiens (human) 5925 RB1
  • PMID:11204276
DOID:3454 brain infarction HGNC:259 Homo sapiens (human) 133 ADM
  • PMID:21695352
DOID:10608 celiac disease HGNC:3535 Homo sapiens (human) 2147 F2
  • PMID:23556408
DOID:2741 bilirubin metabolic disorder HGNC:4893 Homo sapiens (human) 3082 HGF
  • PMID:9073133
DOID:4492 avian influenza HGNC:13557 Homo sapiens (human) 59272 ACE2
  • PMID:24800825
DOID:9952 acute lymphoblastic leukemia HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:17317918
  • PMID:24698347
DOID:2723 dermatitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:3171214
DOID:14069 cerebral malaria HGNC:7997 Homo sapiens (human) 3084 NRG1
  • PMID:24433482
DOID:784 chronic kidney disease RGD:3273 Rattus norvegicus (Norway rat) 25121 Pcsk2
  • PMID:18039782
DOID:4947 cholangiocarcinoma HGNC:11936 Homo sapiens (human) 356 FASLG
  • PMID:11029528
DOID:224 transient cerebral ischemia HGNC:11760 Homo sapiens (human) 7035 TFPI
  • PMID:18067952
DOID:0080855 Parkinsonism RGD:620144 Rattus norvegicus (Norway rat) 59109 Ntrk1
  • PMID:20581854

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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: December 9, 2024