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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 8976 - 9000 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:12930 dilated cardiomyopathy HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:26893848
DOID:9976 heroin dependence HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:24016178
  • PMID:24956251
DOID:13922 eosinophilic esophagitis HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:26416193
DOID:0111223 centronuclear myopathy 1 HGNC:26190 Homo sapiens (human) 64419 MTMR14
  • RGD:7240710
DOID:0112315 brain small vessel disease 3 HGNC:26182 Homo sapiens (human) 79709 COLGALT1
  • RGD:7240710
DOID:9974 drug dependence HGNC:2615 Homo sapiens (human) 1555 CYP2B6
  • PMID:24455721
DOID:0050742 nicotine dependence HGNC:2615 Homo sapiens (human) 1555 CYP2B6
  • PMID:17223085
  • PMID:17654295
  • PMID:25489907
DOID:9970 obesity HGNC:2615 Homo sapiens (human) 1555 CYP2B6
  • MGI:6194238
DOID:9828 neonatal abstinence syndrome HGNC:2615 Homo sapiens (human) 1555 CYP2B6
  • PMID:28320034
DOID:1596 depressive disorder HGNC:2615 Homo sapiens (human) 1555 CYP2B6
  • MGI:6194238
DOID:9976 heroin dependence HGNC:2615 Homo sapiens (human) 1555 CYP2B6
  • PMID:21790905
DOID:9119 acute myeloid leukemia HGNC:2615 Homo sapiens (human) 1555 CYP2B6
  • PMID:19144407
DOID:399 tuberculosis HGNC:2615 Homo sapiens (human) 1555 CYP2B6
  • PMID:28389387
  • PMID:30239753
DOID:526 human immunodeficiency virus infectious disease HGNC:2615 Homo sapiens (human) 1555 CYP2B6
  • PMID:18281305
  • PMID:21862974
DOID:0070311 oligoasthenoteratozoospermia HGNC:26125 Homo sapiens (human) 64847 SPATA20
  • 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

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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