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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 4901 - 4925 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9744 type 1 diabetes mellitus HGNC:6619 Homo sapiens (human) 3990 LIPC
  • PMID:9580247
DOID:2237 hepatitis HGNC:6619 Homo sapiens (human) 3990 LIPC
  • MGI:6194238
DOID:1168 familial hyperlipidemia HGNC:6619 Homo sapiens (human) 3990 LIPC
  • MGI:6194238
DOID:1312 focal segmental glomerulosclerosis HGNC:6619 Homo sapiens (human) 3990 LIPC
  • MGI:6194238
DOID:783 end stage renal disease HGNC:6619 Homo sapiens (human) 3990 LIPC
  • MGI:6194238
DOID:557 kidney disease HGNC:6619 Homo sapiens (human) 3990 LIPC
  • PMID:15983323
  • PMID:16928730
DOID:10652 Alzheimer's disease HGNC:6619 Homo sapiens (human) 3990 LIPC
  • PMID:17175070
DOID:341 peripheral vascular disease HGNC:6619 Homo sapiens (human) 3990 LIPC
  • PMID:18413186
DOID:1459 hypothyroidism HGNC:6619 Homo sapiens (human) 3990 LIPC
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:6619 Homo sapiens (human) 3990 LIPC
  • PMID:15656877
  • PMID:16429317
  • RGD:7240710
DOID:11801 protein-energy malnutrition HGNC:6619 Homo sapiens (human) 3990 LIPC
  • MGI:6194238
DOID:9970 obesity HGNC:6619 Homo sapiens (human) 3990 LIPC
  • MGI:6194238
  • PMID:12843191
DOID:326 ischemia HGNC:6619 Homo sapiens (human) 3990 LIPC
  • MGI:6194238
DOID:13809 familial combined hyperlipidemia HGNC:6619 Homo sapiens (human) 3990 LIPC
  • PMID:16338252
DOID:3393 coronary artery disease HGNC:6619 Homo sapiens (human) 3990 LIPC
  • PMID:11916946
  • PMID:12689525
  • PMID:15099346
  • PMID:33004870
DOID:1184 nephrotic syndrome HGNC:6619 Homo sapiens (human) 3990 LIPC
  • MGI:6194238
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
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:9970 obesity HGNC:6677 Homo sapiens (human) 4023 LPL
  • 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