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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 70326 - 70350 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1793 pancreatic cancer HGNC:1571 Homo sapiens (human) 887 CCKBR
  • MGI:6194238
  • PMID:15688412
DOID:14115 toxic shock syndrome HGNC:1571 Homo sapiens (human) 887 CCKBR
  • MGI:6194238
DOID:0081312 T-cell non-Hodgkin lymphoma HGNC:5392 Homo sapiens (human) 8870 IER3
  • PMID:14534530
DOID:0060894 early-onset Parkinson's disease HGNC:11504 Homo sapiens (human) 8871 SYNJ2
  • MGI:6194238
DOID:14250 Down syndrome HGNC:11504 Homo sapiens (human) 8871 SYNJ2
  • MGI:6194238
DOID:14330 Parkinson's disease HGNC:11504 Homo sapiens (human) 8871 SYNJ2
  • MGI:6194238
DOID:6713 cerebrovascular disease HGNC:15607 Homo sapiens (human) 8874 ARHGEF7
  • MGI:6194238
DOID:3498 pancreatic ductal adenocarcinoma HGNC:12705 Homo sapiens (human) 8876 VNN1
  • PMID:32663515
DOID:299 adenocarcinoma HGNC:11240 Homo sapiens (human) 8877 SPHK1
  • MGI:6194238
DOID:0050700 cardiomyopathy HGNC:11240 Homo sapiens (human) 8877 SPHK1
  • MGI:6194238
DOID:3070 high grade glioma HGNC:11240 Homo sapiens (human) 8877 SPHK1
  • MGI:6194238
DOID:9970 obesity HGNC:11240 Homo sapiens (human) 8877 SPHK1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:11240 Homo sapiens (human) 8877 SPHK1
  • PMID:17265031
DOID:0081363 distal myopathy with rimmed vacuoles HGNC:11280 Homo sapiens (human) 8878 SQSTM1
  • RGD:7240710
DOID:0081364 neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset HGNC:11280 Homo sapiens (human) 8878 SQSTM1
  • MGI:6194238
  • RGD:7240710
DOID:10763 hypertension HGNC:11280 Homo sapiens (human) 8878 SQSTM1
  • MGI:6194238
DOID:332 amyotrophic lateral sclerosis HGNC:11280 Homo sapiens (human) 8878 SQSTM1
  • MGI:6194238
DOID:1686 glaucoma HGNC:11280 Homo sapiens (human) 8878 SQSTM1
  • MGI:6194238
DOID:0110068 frontotemporal dementia and/or amyotrophic lateral sclerosis 3 HGNC:11280 Homo sapiens (human) 8878 SQSTM1
  • RGD:7240710
DOID:0081366 Paget's disease of bone 3 HGNC:11280 Homo sapiens (human) 8878 SQSTM1
  • RGD:7240710
DOID:5408 Paget's disease of bone HGNC:11280 Homo sapiens (human) 8878 SQSTM1
  • MGI:6194238
  • PMID:11992264
DOID:10595 Charcot-Marie-Tooth disease HGNC:10817 Homo sapiens (human) 8879 SGPL1
  • MGI:6194238
DOID:1184 nephrotic syndrome HGNC:10817 Homo sapiens (human) 8879 SGPL1
  • MGI:6194238
DOID:9970 obesity HGNC:10817 Homo sapiens (human) 8879 SGPL1
  • MGI:6194238
DOID:0080265 nephrotic syndrome type 14 HGNC:10817 Homo sapiens (human) 8879 SGPL1
  • 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: December 9, 2024