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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 October 9, 2024
Displaying entries 71726 - 71750 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:526 human immunodeficiency virus infectious disease HGNC:40 Homo sapiens (human) 5243 ABCB1
  • MGI:6194238
  • PMID:23133441
  • PMID:27334660
DOID:1824 status epilepticus HGNC:40 Homo sapiens (human) 5243 ABCB1
  • MGI:6194238
DOID:8577 ulcerative colitis HGNC:40 Homo sapiens (human) 5243 ABCB1
  • PMID:15505619
DOID:4481 allergic rhinitis HGNC:40 Homo sapiens (human) 5243 ABCB1
  • PMID:24040855
DOID:10939 antisocial personality disorder HGNC:40 Homo sapiens (human) 5243 ABCB1
  • PMID:25918995
DOID:684 hepatocellular carcinoma HGNC:40 Homo sapiens (human) 5243 ABCB1
  • MGI:6194238
  • PMID:23488625
  • PMID:24175826
DOID:2987 familial mediterranean fever HGNC:40 Homo sapiens (human) 5243 ABCB1
  • PMID:17610314
  • PMID:23408444
  • PMID:24773260
DOID:2957 pulmonary tuberculosis HGNC:40 Homo sapiens (human) 5243 ABCB1
  • PMID:26067842
DOID:1168 familial hyperlipidemia HGNC:40 Homo sapiens (human) 5243 ABCB1
  • PMID:26922556
DOID:12365 malaria HGNC:40 Homo sapiens (human) 5243 ABCB1
  • PMID:17015054
  • PMID:19331170
  • PMID:28422980
  • PMID:28934955
DOID:2154 nephroblastoma HGNC:40 Homo sapiens (human) 5243 ABCB1
  • PMID:11888090
DOID:2917 cryoglobulinemia HGNC:40 Homo sapiens (human) 5243 ABCB1
  • PMID:28453396
DOID:0060750 familial temporal lobe epilepsy 3 HGNC:40 Homo sapiens (human) 5243 ABCB1
  • PMID:24590840
DOID:13413 hepatic encephalopathy HGNC:40 Homo sapiens (human) 5243 ABCB1
  • MGI:6194238
DOID:783 end stage renal disease HGNC:40 Homo sapiens (human) 5243 ABCB1
  • MGI:6194238
DOID:3328 temporal lobe epilepsy HGNC:40 Homo sapiens (human) 5243 ABCB1
  • MGI:6194238
DOID:635 acquired immunodeficiency syndrome HGNC:40 Homo sapiens (human) 5243 ABCB1
  • PMID:23372834
  • PMID:24517233
DOID:0111364 Alzheimer's disease 9 HGNC:37 Homo sapiens (human) 10347 ABCA7
  • RGD:7240710
DOID:0050817 Stargardt disease HGNC:34 Homo sapiens (human) 24 ABCA4
  • MGI:6194238
DOID:0110015 age related macular degeneration 2 HGNC:34 Homo sapiens (human) 24 ABCA4
  • RGD:7240710
DOID:4448 macular degeneration HGNC:34 Homo sapiens (human) 24 ABCA4
  • PMID:9295268
DOID:8501 fundus dystrophy HGNC:34 Homo sapiens (human) 24 ABCA4
  • PMID:16546111
DOID:0110354 retinitis pigmentosa 19 HGNC:34 Homo sapiens (human) 24 ABCA4
  • MGI:6194238
  • RGD:7240710
DOID:8466 retinal degeneration HGNC:34 Homo sapiens (human) 24 ABCA4
  • PMID:22661473
DOID:0111013 cone-rod dystrophy 3 HGNC:34 Homo sapiens (human) 24 ABCA4
  • MGI:6194238
  • RGD:7240710

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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: December 9, 2024