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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 3201 - 3225 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:9352 type 2 diabetes mellitus HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:19936701
DOID:8947 diabetic retinopathy HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:11311965
DOID:5022 aflatoxins-related hepatocellular carcinoma HGNC:4250 Homo sapiens (human) 2678 GGT1
  • MGI:6194238
DOID:0050741 alcohol dependence HGNC:4250 Homo sapiens (human) 2678 GGT1
  • MGI:6194238
DOID:9351 diabetes mellitus HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:17888134
DOID:0080546 non-alcoholic fatty liver HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:23730648
DOID:1909 melanoma HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:6120756
DOID:9452 steatotic liver disease HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:19670414
DOID:11714 gestational diabetes HGNC:4250 Homo sapiens (human) 2678 GGT1
  • PMID:18937705
DOID:4914 esophagus adenocarcinoma HGNC:18129 Homo sapiens (human) 51738 GHRL
  • PMID:21472143
DOID:9352 type 2 diabetes mellitus HGNC:18129 Homo sapiens (human) 51738 GHRL
  • PMID:18848536
DOID:3125 multiple endocrine neoplasia HGNC:18129 Homo sapiens (human) 51738 GHRL
  • MGI:6194238
DOID:11983 Prader-Willi syndrome HGNC:18129 Homo sapiens (human) 51738 GHRL
  • PMID:15057669
DOID:783 end stage renal disease HGNC:18129 Homo sapiens (human) 51738 GHRL
  • PMID:18809976
DOID:3525 middle cerebral artery infarction HGNC:18129 Homo sapiens (human) 51738 GHRL
  • MGI:6194238
DOID:1287 cardiovascular system disease HGNC:18129 Homo sapiens (human) 51738 GHRL
  • PMID:20930430
DOID:11981 morbid obesity HGNC:18129 Homo sapiens (human) 51738 GHRL
  • PMID:19188925
DOID:9743 diabetic neuropathy HGNC:18129 Homo sapiens (human) 51738 GHRL
  • PMID:19733151
DOID:9970 obesity HGNC:18129 Homo sapiens (human) 51738 GHRL
  • RGD:7240710
DOID:0050848 obstructive sleep apnea HGNC:18129 Homo sapiens (human) 51738 GHRL
  • MGI:6194238
DOID:1574 alcohol use disorder SGD:S000000856 Saccharomyces cerevisiae S288C 856781 GIP2
  • MGI:6194238
DOID:9993 hypoglycemia SGD:S000000856 Saccharomyces cerevisiae S288C 856781 GIP2
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus SGD:S000000856 Saccharomyces cerevisiae S288C 856781 GIP2
  • MGI:6194238
DOID:0060363 glycerol kinase deficiency HGNC:4289 Homo sapiens (human) 2710 GK
  • MGI:6194238
  • PMID:9719371
  • RGD:7240710
DOID:13810 familial hypercholesterolemia HGNC:4289 Homo sapiens (human) 2710 GK
  • MGI:6194238

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Supported by JST NBDC Grant Number JPMJND2204

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