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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 3026 - 3050 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0112136 severe congenital neutropenia 4 HGNC:24861 Homo sapiens (human) 92579 G6PC3
  • RGD:7240710
DOID:0070254 congenital disorder of glycosylation type IIb HGNC:24862 Homo sapiens (human) 7841 MOGS
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:24864 Homo sapiens (human) 26330 GAPDHS
  • PMID:15507493
DOID:1184 nephrotic syndrome HGNC:24865 Homo sapiens (human) 57678 GPAM
  • MGI:6194238
DOID:9970 obesity HGNC:24865 Homo sapiens (human) 57678 GPAM
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:24865 Homo sapiens (human) 57678 GPAM
  • MGI:6194238
DOID:0111420 familial GPIHBP1 deficiency HGNC:24945 Homo sapiens (human) 338328 GPIHBP1
  • RGD:7240710
DOID:0050741 alcohol dependence HGNC:250 Homo sapiens (human) 125 ADH1B
  • RGD:7240710
DOID:0110515 autosomal recessive nonsyndromic deafness 63 HGNC:25033 Homo sapiens (human) 220074 LRTOMT
  • MGI:6194238
  • RGD:7240710
DOID:1793 pancreatic cancer HGNC:251 Homo sapiens (human) 126 ADH1C
  • PMID:19068087
DOID:0060892 late onset Parkinson's disease HGNC:251 Homo sapiens (human) 126 ADH1C
  • RGD:7240710
DOID:0050741 alcohol dependence HGNC:251 Homo sapiens (human) 126 ADH1C
  • RGD:7240710
DOID:2977 primary hyperoxaluria HGNC:25155 Homo sapiens (human) 112817 HOGA1
  • MGI:6194238
DOID:0111672 primary hyperoxaluria type 3 HGNC:25155 Homo sapiens (human) 112817 HOGA1
  • RGD:7240710
DOID:1064 cystinosis HGNC:2518 Homo sapiens (human) 1497 CTNS
  • MGI:6194238
  • PMID:10068513
  • PMID:11565547
  • PMID:18578013
  • PMID:9537412
  • PMID:9792862
  • RGD:7240710
DOID:1062 Fanconi syndrome HGNC:2518 Homo sapiens (human) 1497 CTNS
  • MGI:6194238
DOID:0050741 alcohol dependence HGNC:252 Homo sapiens (human) 127 ADH4
  • PMID:20077761
DOID:1184 nephrotic syndrome HGNC:25223 Homo sapiens (human) 27235 COQ2
  • MGI:6194238
DOID:0050730 coenzyme Q10 deficiency disease HGNC:25223 Homo sapiens (human) 27235 COQ2
  • MGI:6194238
DOID:4752 multiple system atrophy HGNC:25223 Homo sapiens (human) 27235 COQ2
  • MGI:6194238
DOID:0070238 primary coenzyme Q10 deficiency 1 HGNC:25223 Homo sapiens (human) 27235 COQ2
  • MGI:6194238
  • RGD:7240710
DOID:10603 glucose intolerance HGNC:25223 Homo sapiens (human) 27235 COQ2
  • MGI:6194238
DOID:12798 mucopolysaccharidosis HGNC:25239 Homo sapiens (human) 153642 ARSK
  • MGI:6194238
  • RGD:7240710
DOID:2841 asthma HGNC:253 Homo sapiens (human) 128 ADH5
  • PMID:17543375
  • PMID:19395503
  • PMID:19514054
DOID:0080952 AMED syndrome HGNC:253 Homo sapiens (human) 128 ADH5
  • RGD:7240710

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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