Table Filtering
Other Information
Release Statistics Download
Guidelines
MIRAGE
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 65726 - 65750 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0080941 acquired angioedema HGNC:3530 Homo sapiens (human) 2161 F12
  • PMID:9129025
DOID:224 transient cerebral ischemia HGNC:3530 Homo sapiens (human) 2161 F12
  • PMID:16533887
DOID:3525 middle cerebral artery infarction HGNC:3530 Homo sapiens (human) 2161 F12
  • PMID:16533887
DOID:9352 type 2 diabetes mellitus HGNC:3530 Homo sapiens (human) 2161 F12
  • PMID:7974333
DOID:9279 hyperhomocysteinemia HGNC:3530 Homo sapiens (human) 2161 F12
  • MGI:6194238
DOID:2231 factor XII deficiency HGNC:3530 Homo sapiens (human) 2161 F12
  • MGI:6194238
  • PMID:11248286
  • PMID:18024408
  • PMID:20386432
  • PMID:2510163
  • RGD:7240710
DOID:0080940 hereditary angioedema type III HGNC:3530 Homo sapiens (human) 2161 F12
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:3530 Homo sapiens (human) 2161 F12
  • PMID:16411408
DOID:3490 Noonan syndrome HGNC:3529 Homo sapiens (human) 2160 F11
  • PMID:3354599
DOID:0060903 thrombosis HGNC:3529 Homo sapiens (human) 2160 F11
  • PMID:19583818
  • PMID:22633531
DOID:2229 factor XI deficiency HGNC:3529 Homo sapiens (human) 2160 F11
  • MGI:6194238
  • PMID:10706758
  • PMID:11127865
  • PMID:2813350
  • RGD:7240710
DOID:2222 factor X deficiency HGNC:3528 Homo sapiens (human) 2159 F10
  • PMID:22008904
  • PMID:2790181
  • RGD:7240710
DOID:1612 breast cancer HGNC:3528 Homo sapiens (human) 2159 F10
  • PMID:25407022
DOID:9279 hyperhomocysteinemia HGNC:3528 Homo sapiens (human) 2159 F10
  • MGI:6194238
DOID:0111899 X-linked thrombophilia due to factor IX defect HGNC:3551 Homo sapiens (human) 2158 F9
  • RGD:7240710
DOID:12259 hemophilia B HGNC:3551 Homo sapiens (human) 2158 F9
  • MGI:6194238
  • PMID:20351275
  • PMID:2041805
  • PMID:21122306
  • PMID:2714791
  • PMID:2752145
  • RGD:7240710
DOID:0080839 X-linked warfarin sensitivity HGNC:3551 Homo sapiens (human) 2158 F9
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:3551 Homo sapiens (human) 2158 F9
  • PMID:7974333
DOID:12134 factor VIII deficiency HGNC:3546 Homo sapiens (human) 2157 F8
  • MGI:6194238
  • PMID:10468616
  • PMID:10612839
  • PMID:16786531
  • RGD:7240710
DOID:0060574 von Willebrand's disease 2 HGNC:3546 Homo sapiens (human) 2157 F8
  • PMID:16409463
DOID:9279 hyperhomocysteinemia HGNC:3546 Homo sapiens (human) 2157 F8
  • MGI:6194238
DOID:801 hemarthrosis HGNC:3546 Homo sapiens (human) 2157 F8
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:3546 Homo sapiens (human) 2157 F8
  • PMID:7974333
DOID:9351 diabetes mellitus HGNC:3544 Homo sapiens (human) 2155 F7
  • MGI:6194238
DOID:1588 thrombocytopenia HGNC:3544 Homo sapiens (human) 2155 F7
  • PMID:19175492

About Release Notes Help Feedback

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 v4.1.1

Last updated: February 17, 2025