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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 7201 - 7225 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:2747 glycogen storage disease Xenbase:XB-GENE-852729 Xenopus tropicalis (tropical clawed frog) 394883 gyg1
  • MGI:6194238
DOID:0080567 congenital disorder of glycosylation Ip Xenbase:XB-GENE-5934131 Xenopus tropicalis (tropical clawed frog) 394898 alg11
  • MGI:6194238
DOID:784 chronic kidney disease Xenbase:XB-GENE-1017054 Xenopus tropicalis (tropical clawed frog) 395003 dgat2
  • MGI:6194238
DOID:10787 premature menopause Xenbase:XB-GENE-1017054 Xenopus tropicalis (tropical clawed frog) 395003 dgat2
  • MGI:6194238
DOID:9452 steatotic liver disease Xenbase:XB-GENE-1017054 Xenopus tropicalis (tropical clawed frog) 395003 dgat2
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease Xenbase:XB-GENE-1017054 Xenopus tropicalis (tropical clawed frog) 395003 dgat2
  • MGI:6194238
DOID:2018 hyperinsulinism HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
DOID:0050741 alcohol dependence HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
  • PMID:29912265
DOID:5016 hepatocellular clear cell carcinoma HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:20723213
DOID:783 end stage renal disease HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:9294834
DOID:0111334 congenital leptin deficiency HGNC:6553 Homo sapiens (human) 3952 LEP
  • RGD:7240710
DOID:0050848 obstructive sleep apnea HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:18606530
DOID:3083 chronic obstructive pulmonary disease HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:20021311
  • PMID:20854423
  • PMID:21367591
DOID:12236 primary biliary cholangitis HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:16093869
DOID:11714 gestational diabetes HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:19269197
DOID:4483 rhinitis HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:19860581
DOID:684 hepatocellular carcinoma HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
  • PMID:18573568
  • PMID:28452232
DOID:0060611 abdominal obesity-metabolic syndrome HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
DOID:2913 acute pancreatitis HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
DOID:10603 glucose intolerance HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
DOID:9452 steatotic liver disease HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
  • PMID:28281237
DOID:10591 pre-eclampsia HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
DOID:14221 abdominal obesity-metabolic syndrome 1 HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
DOID:1612 breast cancer HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:16019138
DOID:4450 renal cell carcinoma HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:19278051

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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