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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 7376 - 7400 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
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
DOID:12858 Huntington's disease HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
  • PMID:18564365
DOID:1485 cystic fibrosis HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:18353734
DOID:10652 Alzheimer's disease HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
  • PMID:9755363
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
  • PMID:18713300
  • PMID:20476641
  • PMID:30052309
DOID:11476 osteoporosis HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
  • PMID:11459801
  • PMID:21376149
DOID:14330 Parkinson's disease HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
DOID:10763 hypertension HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
  • PMID:19204185
DOID:1168 familial hyperlipidemia HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
DOID:11394 adult respiratory distress syndrome HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:21317313
DOID:2841 asthma HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:19705789
DOID:8398 osteoarthritis HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:14613274
DOID:3908 lung non-small cell carcinoma HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:19033693
DOID:14018 alcoholic liver cirrhosis HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
  • PMID:29912265
DOID:9970 obesity HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
  • PMID:15910756
  • PMID:19267279
DOID:10605 short bowel syndrome HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238

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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