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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 4376 - 4400 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:3525 middle cerebral artery infarction HGNC:30308 Homo sapiens (human) 56963 RGMA
  • MGI:6194238
DOID:0080566 congenital disorder of glycosylation In SGD:S000000116 Saccharomyces cerevisiae S288C 852261 RFT1
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I HGNC:30220 Homo sapiens (human) 91869 RFT1
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I SGD:S000000116 Saccharomyces cerevisiae S288C 852261 RFT1
  • PMID:18313027
DOID:162 cancer SGD:S000000116 Saccharomyces cerevisiae S288C 852261 RFT1
  • PMID:26354769
DOID:162 cancer HGNC:30220 Homo sapiens (human) 91869 RFT1
  • MGI:6194238
DOID:0080566 congenital disorder of glycosylation In HGNC:30220 Homo sapiens (human) 91869 RFT1
  • RGD:7240710
DOID:11446 sciatic neuropathy HGNC:29595 Homo sapiens (human) 130120 REG3G
  • MGI:6194238
DOID:11832 visual epilepsy HGNC:29595 Homo sapiens (human) 130120 REG3G
  • MGI:6194238
DOID:552 pneumonia HGNC:29595 Homo sapiens (human) 130120 REG3G
  • MGI:6194238
DOID:2913 acute pancreatitis HGNC:29595 Homo sapiens (human) 130120 REG3G
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:29595 Homo sapiens (human) 130120 REG3G
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:9952 Homo sapiens (human) 5968 REG1B
  • MGI:6194238
DOID:219 colon cancer HGNC:9952 Homo sapiens (human) 5968 REG1B
  • MGI:6194238
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
DOID:784 chronic kidney disease HGNC:9922 Homo sapiens (human) 5950 RBP4
  • PMID:21817822
DOID:10591 pre-eclampsia HGNC:9922 Homo sapiens (human) 5950 RBP4
  • PMID:21173508
  • PMID:21299359

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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