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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 3476 - 3500 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:11832 visual epilepsy HGNC:9068 Homo sapiens (human) 5338 PLD2
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:19949019
DOID:5082 liver cirrhosis HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:5383 Homo sapiens (human) 3418 IDH2
  • PMID:24716838
DOID:0111135 congenital generalized lipodystrophy type 1 HGNC:325 Homo sapiens (human) 10555 AGPAT2
  • MGI:6194238
  • RGD:7240710
DOID:2870 endometrial adenocarcinoma HGNC:11998 Homo sapiens (human) 7157 TP53
  • PMID:1540970
DOID:3454 brain infarction HGNC:404 Homo sapiens (human) 217 ALDH2
  • PMID:17388993
DOID:9970 obesity HGNC:9056 Homo sapiens (human) 5331 PLCB3
  • MGI:6194238
DOID:9351 diabetes mellitus HGNC:11007 Homo sapiens (human) 6515 SLC2A3
  • PMID:10086067
DOID:0080600 COVID-19 HGNC:1027 Homo sapiens (human) 622 BDH1
  • PMID:32456948
DOID:684 hepatocellular carcinoma HGNC:587 Homo sapiens (human) 328 APEX1
  • MGI:6194238
DOID:12399 pathological gambling HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • PMID:22740152
DOID:0060292 X-linked chondrodysplasia punctata 1 HGNC:13398 Homo sapiens (human) 50814 NSDHL
  • MGI:6194238
DOID:0014667 disease of metabolism HGNC:6081 Homo sapiens (human) 3630 INS
  • PMID:22151886
DOID:1184 nephrotic syndrome HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:12918 thromboangiitis obliterans HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • MGI:6194238
  • PMID:12086338
DOID:9869 hereditary fructose intolerance syndrome HGNC:417 Homo sapiens (human) 229 ALDOB
  • PMID:15532022
  • PMID:8096362
  • RGD:7240710
DOID:10763 hypertension HGNC:17855 Homo sapiens (human) 26035 GLCE
  • PMID:27699767
DOID:3454 brain infarction HGNC:13633 Homo sapiens (human) 9370 ADIPOQ
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:30092 Homo sapiens (human) 10135 NAMPT
  • MGI:6194238
  • PMID:25603815
DOID:2917 cryoglobulinemia HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:19860001
DOID:1612 breast cancer HGNC:1932 Homo sapiens (human) 1116 CHI3L1
  • PMID:12889595
DOID:9408 acute myocardial infarction HGNC:9588 Homo sapiens (human) 5728 PTEN
  • MGI:6194238
  • PMID:32595526
DOID:4914 esophagus adenocarcinoma HGNC:2594 Homo sapiens (human) 1588 CYP19A1
  • PMID:21472143
DOID:10652 Alzheimer's disease HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:12962917
  • PMID:15468911
  • PMID:16516271
  • PMID:16908746
  • PMID:18834925
  • PMID:18992723
  • PMID:9772027

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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: August 19, 2024