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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 726 - 750 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:9970 obesity HGNC:3569 Homo sapiens (human) 2180 ACSL1
  • MGI:6194238
  • PMID:16788709
DOID:9970 obesity RGD:2082 Rattus norvegicus (Norway rat) 25233 Akt2
  • MGI:6194238
  • PMID:18508911
DOID:9970 obesity HGNC:6619 Homo sapiens (human) 3990 LIPC
  • MGI:6194238
  • PMID:12843191
DOID:10325 silicosis RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
  • PMID:25199287
DOID:9352 type 2 diabetes mellitus HGNC:4056 Homo sapiens (human) 2538 G6PC1
  • MGI:6194238
  • PMID:10866049
DOID:9256 colorectal cancer HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
  • PMID:11756242
DOID:5844 myocardial infarction HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
  • PMID:20467748
DOID:0050855 renal fibrosis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:10504496
DOID:5082 liver cirrhosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:19695831
DOID:0080208 metabolic dysfunction-associated steatotic liver disease RGD:3000 Rattus norvegicus (Norway rat) 25608 Lep
  • MGI:6194238
  • PMID:20476641
  • PMID:30052309
DOID:6000 congestive heart failure HGNC:288 Homo sapiens (human) 155 ADRB3
  • MGI:6194238
  • PMID:11273992
DOID:783 end stage renal disease RGD:620396 Rattus norvegicus (Norway rat) 83504 Kl
  • MGI:6194238
  • PMID:9731228
DOID:9352 type 2 diabetes mellitus RGD:69247 Rattus norvegicus (Norway rat) 83535 Kcnj11
  • MGI:6194238
  • PMID:24681897
DOID:9970 obesity HGNC:392 Homo sapiens (human) 208 AKT2
  • MGI:6194238
  • PMID:12663464
DOID:13088 periventricular leukomalacia HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:8652010
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:12518 Homo sapiens (human) 7351 UCP2
  • MGI:6194238
  • PMID:18308829
DOID:684 hepatocellular carcinoma HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
  • PMID:19422879
DOID:3070 high grade glioma HGNC:23059 Homo sapiens (human) 63827 BCAN
  • MGI:6194238
  • PMID:16061654
  • PMID:23253190
DOID:4989 pancreatitis HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
  • PMID:12923961
DOID:4450 renal cell carcinoma RGD:621168 Rattus norvegicus (Norway rat) 81528 Ogg1
  • MGI:6194238
  • PMID:18218111
DOID:4677 keratitis HGNC:11848 Homo sapiens (human) 7097 TLR2
  • MGI:6194238
  • PMID:18398706
DOID:9870 galactosemia SGD:S000000222 Saccharomyces cerevisiae S288C 852306 GAL7
  • MGI:6194238
  • PMID:10799308
  • PMID:24077966
  • PMID:28213126
  • PMID:8794735
DOID:0080552 congenital disorder of glycosylation Ia SGD:S000001849 Saccharomyces cerevisiae S288C 850499 SEC53
  • MGI:6194238
  • PMID:30530630
  • PMID:36214454
DOID:0050884 triosephosphate isomerase deficiency SGD:S000002457 Saccharomyces cerevisiae S288C 851620 TPI1
  • MGI:6194238
  • PMID:24598263
DOID:0080433 developmental and epileptic encephalopathy 51 SGD:S000001568 Saccharomyces cerevisiae S288C 853777 MDH1
  • MGI:6194238
  • PMID:27989324

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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