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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 3201 - 3225 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:6432 pulmonary hypertension HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • MGI:6194238
  • PMID:28202489
DOID:0080855 Parkinsonism HGNC:4616 Homo sapiens (human) 2931 GSK3A
  • MGI:6194238
DOID:2871 endometrial carcinoma HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:18519763
DOID:3587 pancreatic ductal carcinoma HGNC:3148 Homo sapiens (human) 1890 TYMP
  • PMID:19760965
DOID:10605 short bowel syndrome HGNC:6554 Homo sapiens (human) 3953 LEPR
  • MGI:6194238
DOID:11624 penile benign neoplasm HGNC:9599 Homo sapiens (human) 9536 PTGES
  • PMID:14871981
DOID:6000 congestive heart failure HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:10618301
DOID:11713 diabetic angiopathy HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:18575614
DOID:2738 pseudoxanthoma elasticum HGNC:3356 Homo sapiens (human) 5167 ENPP1
  • MGI:6194238
DOID:4483 rhinitis HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:16950285
  • PMID:20109306
DOID:114 heart disease HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • MGI:6194238
DOID:8577 ulcerative colitis HGNC:4554 Homo sapiens (human) 2877 GPX2
  • PMID:18479189
DOID:3393 coronary artery disease HGNC:6623 Homo sapiens (human) 9388 LIPG
  • PMID:16354105
DOID:0050891 adrenal cortical adenoma HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • PMID:12457455
DOID:1240 leukemia HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:26524016
DOID:5154 borna disease HGNC:418 Homo sapiens (human) 230 ALDOC
  • MGI:6194238
DOID:0112303 spondylometaphyseal dysplasia with corneal dystrophy HGNC:9056 Homo sapiens (human) 5331 PLCB3
  • RGD:7240710
DOID:2394 ovarian cancer HGNC:8125 Homo sapiens (human) 4968 OGG1
  • PMID:24698998
DOID:6000 congestive heart failure HGNC:6563 Homo sapiens (human) 3958 LGALS3
  • MGI:6194238
DOID:2671 transitional cell carcinoma HGNC:9599 Homo sapiens (human) 9536 PTGES
  • MGI:6194238
  • PMID:14499677
DOID:1875 impotence HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:9922 Homo sapiens (human) 5950 RBP4
  • PMID:18854400
  • PMID:21645024
  • PMID:25437889
  • PMID:25479076
  • PMID:31278889
DOID:8947 diabetic retinopathy HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
DOID:820 myocarditis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:9970 obesity HGNC:9155 Homo sapiens (human) 5406 PNLIP
  • MGI:6194238

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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: August 19, 2024