Table Filtering
Other Information
Release Statistics Download
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 7601 - 7625 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▼ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0110292 autosomal recessive limb-girdle muscular dystrophy type 2O HGNC:19139 Homo sapiens (human) 55624 POMGNT1
  • RGD:7240710
DOID:2870 endometrial adenocarcinoma HGNC:4555 Homo sapiens (human) 2878 GPX3
  • MGI:6194238
DOID:898 autosomal dominant polycystic kidney disease HGNC:9009 Homo sapiens (human) 5311 PKD2
  • MGI:6194238
  • PMID:21115670
  • PMID:22863349
DOID:0090101 lethal congenital glycogen storage disease of heart HGNC:9386 Homo sapiens (human) 51422 PRKAG2
  • MGI:6194238
  • RGD:7240710
DOID:2615 papilloma HGNC:9035 Homo sapiens (human) 5321 PLA2G4A
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:12518 Homo sapiens (human) 7351 UCP2
  • MGI:6194238
DOID:409 liver disease HGNC:9411 Homo sapiens (human) 5589 PRKCSH
  • PMID:12529853
DOID:8577 ulcerative colitis HGNC:9604 Homo sapiens (human) 5742 PTGS1
  • MGI:6194238
DOID:3146 lipid metabolism disorder HGNC:14450 Homo sapiens (human) 9663 LPIN2
  • MGI:6194238
DOID:12236 primary biliary cholangitis HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:2911 Homo sapiens (human) 1743 DLST
  • PMID:10227647
DOID:0080555 congenital disorder of glycosylation Ic HGNC:23157 Homo sapiens (human) 29929 ALG6
  • RGD:7240710
DOID:3649 pyruvate decarboxylase deficiency HGNC:8808 Homo sapiens (human) 5162 PDHB
  • PMID:15138885
  • RGD:7240710
DOID:9744 type 1 diabetes mellitus HGNC:1848 Homo sapiens (human) 1056 CEL
  • PMID:10580419
  • PMID:9536927
DOID:9744 type 1 diabetes mellitus HGNC:6081 Homo sapiens (human) 3630 INS
  • MGI:6194238
  • PMID:16113600
  • PMID:16382177
  • PMID:16552513
  • PMID:17284223
  • PMID:17284779
  • PMID:18824271
  • PMID:20535137
  • PMID:21765853
  • PMID:26783749
DOID:0060060 non-Hodgkin lymphoma HGNC:545 Homo sapiens (human) 310 ANXA7
  • PMID:17708571
DOID:1324 lung cancer HGNC:5383 Homo sapiens (human) 3418 IDH2
  • PMID:30128035
DOID:3021 acute kidney failure HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:36583727
DOID:0111898 CK syndrome HGNC:13398 Homo sapiens (human) 50814 NSDHL
  • RGD:7240710
DOID:440 neuromuscular disease HGNC:4458 Homo sapiens (human) 2821 GPI
  • PMID:9856489
DOID:10762 portal hypertension HGNC:435 Homo sapiens (human) 240 ALOX5
  • MGI:6194238
DOID:633 myositis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:10399751
DOID:535 sleep disorder HGNC:11743 Homo sapiens (human) 7021 TFAP2B
  • MGI:6194238
DOID:0050860 colorectal adenoma HGNC:2602 Homo sapiens (human) 1591 CYP24A1
  • PMID:26241700
  • PMID:27978548
DOID:0080998 acute necrotizing pancreatitis HGNC:6107 Homo sapiens (human) 3651 PDX1
  • MGI:6194238

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024