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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 1751 - 1775 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:2605 Homo sapiens (human) 1593 CYP27A1
  • PMID:28774887
DOID:4810 cerebrotendinous xanthomatosis HGNC:2605 Homo sapiens (human) 1593 CYP27A1
  • PMID:2019602
  • RGD:7240710
DOID:0081312 T-cell non-Hodgkin lymphoma MGI:104814 Mus musculus (house mouse) 15937 Ier3
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • PMID:17223345
  • PMID:17606874
DOID:9970 obesity HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • PMID:17223345
DOID:11714 gestational diabetes HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • PMID:36477942
DOID:2043 hepatitis B HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • PMID:22963605
DOID:3021 acute kidney failure HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • MGI:6194238
DOID:10609 rickets HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • MGI:6194238
  • PMID:9486994
DOID:893 Wilson disease HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • MGI:6194238
DOID:10591 pre-eclampsia HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • PMID:22871339
  • PMID:36477942
DOID:2527 nephrosis HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • MGI:6194238
DOID:0080886 vitamin D-dependent rickets type 1A HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • MGI:6194238
  • RGD:7240710
DOID:10283 prostate cancer HGNC:2649 Homo sapiens (human) 1595 CYP51A1
  • MGI:6194238
DOID:9351 diabetes mellitus HGNC:2649 Homo sapiens (human) 1595 CYP51A1
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:2649 Homo sapiens (human) 1595 CYP51A1
  • MGI:6194238
DOID:2377 multiple sclerosis MGI:96434 Mus musculus (house mouse) 16002 Igf2
  • MGI:6194238
DOID:14681 Silver-Russell syndrome MGI:96434 Mus musculus (house mouse) 16002 Igf2
  • MGI:6194238
DOID:9471 meningitis MGI:96434 Mus musculus (house mouse) 16002 Igf2
  • MGI:6194238
DOID:1657 ventricular septal defect MGI:96434 Mus musculus (house mouse) 16002 Igf2
  • MGI:6194238
DOID:8577 ulcerative colitis MGI:96434 Mus musculus (house mouse) 16002 Igf2
  • MGI:6194238
DOID:11476 osteoporosis MGI:96434 Mus musculus (house mouse) 16002 Igf2
  • MGI:6194238
DOID:8398 osteoarthritis MGI:96434 Mus musculus (house mouse) 16002 Igf2
  • MGI:6194238
DOID:14330 Parkinson's disease MGI:96434 Mus musculus (house mouse) 16002 Igf2
  • MGI:6194238
DOID:7148 rheumatoid arthritis MGI:96434 Mus musculus (house mouse) 16002 Igf2
  • MGI:6194238

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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