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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 62426 - 62450 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:783 end stage renal disease HGNC:13345 Homo sapiens (human) 23175 LPIN1
  • MGI:6194238
DOID:811 lipodystrophy HGNC:13345 Homo sapiens (human) 23175 LPIN1
  • MGI:6194238
DOID:11981 morbid obesity HGNC:13345 Homo sapiens (human) 23175 LPIN1
  • PMID:17563064
DOID:3146 lipid metabolism disorder HGNC:13345 Homo sapiens (human) 23175 LPIN1
  • MGI:6194238
DOID:9970 obesity HGNC:13345 Homo sapiens (human) 23175 LPIN1
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:13342 Homo sapiens (human) 51348 KLRF1
  • PMID:35693827
DOID:1826 epilepsy HGNC:13339 Homo sapiens (human) 24137 KIF4A
  • MGI:6194238
DOID:0112040 non-syndromic X-linked intellectual disability 100 HGNC:13339 Homo sapiens (human) 24137 KIF4A
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:13312 Homo sapiens (human) 9446 GSTO1
  • PMID:14570706
  • PMID:15917099
  • PMID:20818931
DOID:1574 alcohol use disorder HGNC:13312 Homo sapiens (human) 9446 GSTO1
  • MGI:6194238
DOID:14330 Parkinson's disease HGNC:13312 Homo sapiens (human) 9446 GSTO1
  • PMID:14570706
  • PMID:17194543
DOID:11394 adult respiratory distress syndrome HGNC:1331 Homo sapiens (human) 727 C5
  • MGI:6194238
  • PMID:3264125
  • PMID:3826891
DOID:2841 asthma HGNC:1331 Homo sapiens (human) 727 C5
  • MGI:6194238
  • PMID:15278436
  • PMID:20143644
DOID:8158 complement component 5 deficiency HGNC:1331 Homo sapiens (human) 727 C5
  • RGD:7240710
DOID:3083 chronic obstructive pulmonary disease HGNC:1331 Homo sapiens (human) 727 C5
  • PMID:20500690
DOID:0060284 paroxysmal nocturnal hemoglobinuria HGNC:1331 Homo sapiens (human) 727 C5
  • RGD:7240710
DOID:1227 neutropenia HGNC:1331 Homo sapiens (human) 727 C5
  • MGI:6194238
  • PMID:10516626
DOID:4724 brain edema HGNC:1331 Homo sapiens (human) 727 C5
  • MGI:6194238
DOID:552 pneumonia HGNC:1331 Homo sapiens (human) 727 C5
  • PMID:3631740
DOID:12134 factor VIII deficiency HGNC:1331 Homo sapiens (human) 727 C5
  • PMID:6912882
DOID:1485 cystic fibrosis HGNC:1331 Homo sapiens (human) 727 C5
  • PMID:3540828
DOID:5082 liver cirrhosis HGNC:1331 Homo sapiens (human) 727 C5
  • PMID:15995705
DOID:0080315 megalencephalic leukoencephalopathy with subcortical cysts HGNC:13308 Homo sapiens (human) 51704 GPRC5B
  • RGD:7240710
DOID:1686 glaucoma HGNC:13299 Homo sapiens (human) 55366 LGR4
  • MGI:6194238
DOID:0050742 nicotine dependence HGNC:13286 Homo sapiens (human) 63979 FIGNL1
  • PMID:16740595

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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