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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 63526 - 63550 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:5419 schizophrenia HGNC:11960 Homo sapiens (human) 26058 GIGYF2
  • MGI:6194238
DOID:14330 Parkinson's disease HGNC:11960 Homo sapiens (human) 26058 GIGYF2
  • RGD:7240710
DOID:0080985 syndromic X-linked intellectual disorder Lujan-Fryns-type HGNC:11957 Homo sapiens (human) 9968 MED12
  • PMID:17369503
  • RGD:7240710
DOID:9970 obesity HGNC:11957 Homo sapiens (human) 9968 MED12
  • MGI:6194238
DOID:1470 major depressive disorder HGNC:11957 Homo sapiens (human) 9968 MED12
  • PMID:12216017
DOID:1967 leiomyosarcoma HGNC:11957 Homo sapiens (human) 9968 MED12
  • PMID:26891131
DOID:14711 FG syndrome HGNC:11957 Homo sapiens (human) 9968 MED12
  • PMID:17334363
  • PMID:20507344
DOID:591 phobic disorder HGNC:11957 Homo sapiens (human) 9968 MED12
  • PMID:12216017
DOID:299 adenocarcinoma HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • MGI:6194238
DOID:114 heart disease HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • MGI:6194238
DOID:0110313 hypertrophic cardiomyopathy 7 HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • MGI:6194238
  • RGD:7240710
DOID:0110460 dilated cardiomyopathy 2A HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • RGD:7240710
DOID:0110459 dilated cardiomyopathy 1FF HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • RGD:7240710
DOID:11984 hypertrophic cardiomyopathy HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • PMID:15698845
DOID:0111425 restrictive cardiomyopathy 1 HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • RGD:7240710
DOID:0050700 cardiomyopathy HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • MGI:6194238
DOID:397 restrictive cardiomyopathy HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • MGI:6194238
  • PMID:16288990
DOID:3393 coronary artery disease HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • PMID:12221049
DOID:12930 dilated cardiomyopathy HGNC:11947 Homo sapiens (human) 7137 TNNI3
  • MGI:6194238
  • PMID:15070570
DOID:0060704 lymphoproliferative syndrome HGNC:11937 Homo sapiens (human) 970 CD70
  • RGD:7240710
DOID:6000 congestive heart failure HGNC:11936 Homo sapiens (human) 356 FASLG
  • MGI:6194238
DOID:7693 abdominal aortic aneurysm HGNC:11936 Homo sapiens (human) 356 FASLG
  • MGI:6194238
DOID:9538 multiple myeloma HGNC:11936 Homo sapiens (human) 356 FASLG
  • PMID:16321857
DOID:3457 invasive lobular carcinoma HGNC:11936 Homo sapiens (human) 356 FASLG
  • PMID:10640988
DOID:0081267 graft-versus-host disease HGNC:11936 Homo sapiens (human) 356 FASLG
  • MGI:6194238
  • PMID:9404931

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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: December 9, 2024