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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 71101 - 71125 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:576 proteinuria HGNC:245 Homo sapiens (human) 120 ADD3
  • MGI:6194238
DOID:13608 biliary atresia HGNC:245 Homo sapiens (human) 120 ADD3
  • MGI:6194238
DOID:10763 hypertension HGNC:244 Homo sapiens (human) 119 ADD2
  • MGI:6194238
  • PMID:16497648
  • PMID:24652215
DOID:2986 IgA glomerulonephritis HGNC:244 Homo sapiens (human) 119 ADD2
  • PMID:19838659
DOID:1969 cerebral palsy HGNC:244 Homo sapiens (human) 119 ADD2
  • MGI:6194238
DOID:0110916 hereditary spherocytosis type 1 HGNC:244 Homo sapiens (human) 119 ADD2
  • MGI:6194238
DOID:0081361 spastic quadriplegic cerebral palsy 3 HGNC:244 Homo sapiens (human) 119 ADD2
  • MGI:6194238
DOID:1936 atherosclerosis HGNC:243 Homo sapiens (human) 118 ADD1
  • PMID:17082469
DOID:2986 IgA glomerulonephritis HGNC:243 Homo sapiens (human) 118 ADD1
  • PMID:19838659
DOID:0081361 spastic quadriplegic cerebral palsy 3 HGNC:243 Homo sapiens (human) 118 ADD1
  • MGI:6194238
DOID:10763 hypertension HGNC:243 Homo sapiens (human) 118 ADD1
  • MGI:6194238
  • PMID:9149697
DOID:13809 familial combined hyperlipidemia HGNC:243 Homo sapiens (human) 118 ADD1
  • PMID:11775124
DOID:3328 temporal lobe epilepsy HGNC:243 Homo sapiens (human) 118 ADD1
  • MGI:6194238
DOID:10908 hydrocephalus HGNC:243 Homo sapiens (human) 118 ADD1
  • MGI:6194238
DOID:11044 gastroschisis HGNC:243 Homo sapiens (human) 118 ADD1
  • PMID:17051589
DOID:1969 cerebral palsy HGNC:243 Homo sapiens (human) 118 ADD1
  • MGI:6194238
DOID:10591 pre-eclampsia HGNC:243 Homo sapiens (human) 118 ADD1
  • PMID:19731222
DOID:10825 essential hypertension HGNC:243 Homo sapiens (human) 118 ADD1
  • RGD:7240710
DOID:5844 myocardial infarction HGNC:243 Homo sapiens (human) 118 ADD1
  • PMID:16420563
  • PMID:17082469
DOID:1574 alcohol use disorder HGNC:242 Homo sapiens (human) 117 ADCYAP1R1
  • MGI:6194238
DOID:2055 post-traumatic stress disorder HGNC:242 Homo sapiens (human) 117 ADCYAP1R1
  • MGI:6194238
DOID:1679 cystitis HGNC:242 Homo sapiens (human) 117 ADCYAP1R1
  • MGI:6194238
DOID:3324 mood disorder HGNC:240 Homo sapiens (human) 115 ADCY9
  • PMID:11840511
DOID:0060558 lethal congenital contracture syndrome HGNC:237 Homo sapiens (human) 112 ADCY6
  • RGD:7240710
DOID:5199 ureteral obstruction HGNC:237 Homo sapiens (human) 112 ADCY6
  • 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: December 9, 2024