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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 5951 - 5975 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:3770 pulmonary fibrosis HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
  • PMID:21681100
DOID:0060074 ductal carcinoma in situ HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:18199541
  • PMID:18237383
DOID:3021 acute kidney failure HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:0060180 colitis HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:2316 brain ischemia HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:162 cancer HGNC:9639 Homo sapiens (human) 9200 HACD1
  • MGI:6194238
DOID:0081337 congenital myopathy HGNC:9639 Homo sapiens (human) 9200 HACD1
  • RGD:7240710
DOID:162 cancer HGNC:9640 Homo sapiens (human) 201562 HACD2
  • MGI:6194238
DOID:3650 lactic acidosis HGNC:9725 Homo sapiens (human) 5836 PYGL
  • MGI:6194238
  • PMID:17705025
DOID:2747 glycogen storage disease HGNC:9725 Homo sapiens (human) 5836 PYGL
  • PMID:9536091
DOID:2754 glycogen storage disease VI HGNC:9725 Homo sapiens (human) 5836 PYGL
  • MGI:6194238
  • PMID:17705025
  • PMID:21646031
  • RGD:7240710
DOID:2746 glycogen storage disease V HGNC:9726 Homo sapiens (human) 5837 PYGM
  • MGI:6194238
  • PMID:9633816
  • RGD:7240710
DOID:13580 cholestasis HGNC:9726 Homo sapiens (human) 5837 PYGM
  • MGI:6194238
DOID:12858 Huntington's disease HGNC:9755 Homo sapiens (human) 23475 QPRT
  • MGI:6194238
DOID:9269 maple syrup urine disease HGNC:986 Homo sapiens (human) 593 BCKDHA
  • PMID:1943689
  • PMID:8037208
  • RGD:7240710
DOID:9269 maple syrup urine disease HGNC:987 Homo sapiens (human) 594 BCKDHB
  • MGI:6194238
  • PMID:2022752
DOID:5082 liver cirrhosis HGNC:9922 Homo sapiens (human) 5950 RBP4
  • PMID:17337499
DOID:12930 dilated cardiomyopathy HGNC:9922 Homo sapiens (human) 5950 RBP4
  • PMID:19926600
DOID:3393 coronary artery disease HGNC:9922 Homo sapiens (human) 5950 RBP4
  • PMID:18854400
  • PMID:21645024
  • PMID:25437889
  • PMID:25479076
  • PMID:31278889
DOID:9970 obesity HGNC:9922 Homo sapiens (human) 5950 RBP4
  • MGI:6194238
  • PMID:17292720
DOID:3526 cerebral infarction HGNC:9922 Homo sapiens (human) 5950 RBP4
  • PMID:19846170
  • PMID:30030781
  • PMID:30038059
DOID:0050912 colon adenoma HGNC:9922 Homo sapiens (human) 5950 RBP4
  • PMID:25712946
DOID:559 acute pyelonephritis HGNC:9922 Homo sapiens (human) 5950 RBP4
  • PMID:20163326
DOID:10763 hypertension HGNC:9922 Homo sapiens (human) 5950 RBP4
  • MGI:6194238
  • PMID:20798476
DOID:5844 myocardial infarction HGNC:9922 Homo sapiens (human) 5950 RBP4
  • PMID:25142320

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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