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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 7276 - 7300 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0080037 Worth syndrome HGNC:6697 Homo sapiens (human) 4041 LRP5
  • RGD:7240710
DOID:11476 osteoporosis HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
  • PMID:17002564
DOID:10159 osteonecrosis HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
DOID:9970 obesity HGNC:6677 Homo sapiens (human) 4023 LPL
  • MGI:6194238
DOID:13809 familial combined hyperlipidemia HGNC:6677 Homo sapiens (human) 4023 LPL
  • RGD:7240710
DOID:1312 focal segmental glomerulosclerosis HGNC:6677 Homo sapiens (human) 4023 LPL
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:6677 Homo sapiens (human) 4023 LPL
  • PMID:18823627
DOID:10652 Alzheimer's disease HGNC:6677 Homo sapiens (human) 4023 LPL
  • PMID:10206232
  • PMID:12133567
  • PMID:15331147
  • PMID:16013913
  • PMID:16965549
  • PMID:24004859
  • PMID:27897113
DOID:14221 abdominal obesity-metabolic syndrome 1 HGNC:6677 Homo sapiens (human) 4023 LPL
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:6677 Homo sapiens (human) 4023 LPL
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:6677 Homo sapiens (human) 4023 LPL
  • MGI:6194238
  • PMID:18321693
  • PMID:18985010
  • PMID:8641022
DOID:0080000 muscular disease HGNC:6677 Homo sapiens (human) 4023 LPL
  • PMID:7635990
DOID:10763 hypertension HGNC:6677 Homo sapiens (human) 4023 LPL
  • PMID:16132104
DOID:14118 familial lipoprotein lipase deficiency HGNC:6677 Homo sapiens (human) 4023 LPL
  • MGI:6194238
  • PMID:16431216
  • PMID:1907278
  • PMID:9973300
  • RGD:7240710
DOID:1168 familial hyperlipidemia HGNC:6677 Homo sapiens (human) 4023 LPL
  • MGI:6194238
  • PMID:9920508
DOID:783 end stage renal disease HGNC:6677 Homo sapiens (human) 4023 LPL
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:6677 Homo sapiens (human) 4023 LPL
  • PMID:8641022
DOID:2211 factor XIII deficiency HGNC:6631 Homo sapiens (human) 3998 LMAN1
  • PMID:9546392
DOID:2216 factor V deficiency HGNC:6631 Homo sapiens (human) 3998 LMAN1
  • PMID:9546392
DOID:10763 hypertension HGNC:6623 Homo sapiens (human) 9388 LIPG
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:6623 Homo sapiens (human) 9388 LIPG
  • PMID:16354105
DOID:1287 cardiovascular system disease HGNC:6623 Homo sapiens (human) 9388 LIPG
  • PMID:16023652
DOID:9970 obesity HGNC:6623 Homo sapiens (human) 9388 LIPG
  • PMID:16772345
DOID:3526 cerebral infarction HGNC:6623 Homo sapiens (human) 9388 LIPG
  • PMID:17016617
DOID:5844 myocardial infarction HGNC:6623 Homo sapiens (human) 9388 LIPG
  • PMID:17526978

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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