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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 5601 - 5625 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:4607 biliary tract cancer HGNC:9235 Homo sapiens (human) 5467 PPARD
  • PMID:18497548
DOID:11151 cholecystolithiasis HGNC:9031 Homo sapiens (human) 5320 PLA2G2A
  • PMID:9695991
DOID:0050156 idiopathic pulmonary fibrosis HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:23260200
DOID:11725 Cornelia de Lange syndrome HGNC:2468 Homo sapiens (human) 9126 SMC3
  • MGI:6194238
DOID:1070 primary open angle glaucoma HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15557444
DOID:2861 congenital nonspherocytic hemolytic anemia HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
  • PMID:1999409
  • PMID:24923766
DOID:10763 hypertension HGNC:6677 Homo sapiens (human) 4023 LPL
  • PMID:16132104
DOID:4810 cerebrotendinous xanthomatosis HGNC:2605 Homo sapiens (human) 1593 CYP27A1
  • PMID:2019602
  • RGD:7240710
DOID:1324 lung cancer HGNC:1097 Homo sapiens (human) 673 BRAF
  • RGD:7240710
DOID:0112376 muscular dystrophy-dystroglycanopathy type B15 HGNC:3007 Homo sapiens (human) 54344 DPM3
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:2468 Homo sapiens (human) 9126 SMC3
  • PMID:29996118
DOID:3827 congenital diaphragmatic hernia HGNC:10798 Homo sapiens (human) 653509 SFTPA1
  • MGI:6194238
DOID:0050328 congenital hypothyroidism HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
DOID:11984 hypertrophic cardiomyopathy HGNC:2595 Homo sapiens (human) 1543 CYP1A1
  • MGI:6194238
DOID:809 cocaine abuse HGNC:5293 Homo sapiens (human) 3356 HTR2A
  • MGI:6194238
DOID:4543 retrograde amnesia HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:2651 Homo sapiens (human) 1581 CYP7A1
  • MGI:6194238
  • PMID:28774887
DOID:3827 congenital diaphragmatic hernia HGNC:5466 Homo sapiens (human) 3481 IGF2
  • MGI:6194238
DOID:8577 ulcerative colitis HGNC:2602 Homo sapiens (human) 1591 CYP24A1
  • PMID:28811712
DOID:162 cancer HGNC:1800 Homo sapiens (human) 1040 CDS1
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • MGI:6194238
DOID:14695 galactokinase deficiency HGNC:4118 Homo sapiens (human) 2584 GALK1
  • RGD:7240710
DOID:4661 multiple chemical sensitivity HGNC:2621 Homo sapiens (human) 1557 CYP2C19
  • PMID:23936614
DOID:2316 brain ischemia HGNC:9603 Homo sapiens (human) 5740 PTGIS
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:6080 Homo sapiens (human) 3636 INPPL1
  • PMID:12086927
  • PMID:15220217

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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