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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 January 28, 2025
Displaying entries 10001 - 10025 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:10159 osteonecrosis HGNC:7876 Homo sapiens (human) 4846 NOS3 inference by association of genotype from phenotype used in manual assertion
  • PMID:28422712
DOID:0050700 cardiomyopathy HGNC:7876 Homo sapiens (human) 4846 NOS3 inference by association of genotype from phenotype used in manual assertion
  • PMID:25699607
DOID:0081398 holoprosencephaly 12 HGNC:7877 Homo sapiens (human) 23019 CNOT1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0081397 Vissers-Bodmer syndrome HGNC:7877 Homo sapiens (human) 23019 CNOT1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050523 adult T-cell leukemia/lymphoma HGNC:7881 Homo sapiens (human) 4851 NOTCH1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16707600
DOID:0080333 aortic valve disease 1 HGNC:7881 Homo sapiens (human) 4851 NOTCH1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16025100
  • RGD:7240710
DOID:1682 congenital heart disease HGNC:7881 Homo sapiens (human) 4851 NOTCH1 inference by association of genotype from phenotype used in manual assertion
  • PMID:31813956
DOID:0060227 Adams-Oliver syndrome HGNC:7881 Homo sapiens (human) 4851 NOTCH1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2736 Hajdu-Cheney syndrome HGNC:7882 Homo sapiens (human) 4853 NOTCH2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9245 Alagille syndrome HGNC:7882 Homo sapiens (human) 4853 NOTCH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16773578
  • RGD:7240710
DOID:0080109 infantile myofibromatosis HGNC:7883 Homo sapiens (human) 4854 NOTCH3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111035 CADASIL 1 HGNC:7883 Homo sapiens (human) 4854 NOTCH3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111343 lateral meningocele syndrome HGNC:7883 Homo sapiens (human) 4854 NOTCH3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060074 ductal carcinoma in situ HGNC:7884 Homo sapiens (human) 4855 NOTCH4 mutant phenotype evidence used in manual assertion
  • PMID:17440163
DOID:1307 dementia HGNC:7884 Homo sapiens (human) 4855 NOTCH4 inference by association of genotype from phenotype used in manual assertion
  • PMID:21297263
DOID:986 alopecia areata HGNC:7884 Homo sapiens (human) 4855 NOTCH4 inference by association of genotype from phenotype used in manual assertion
  • PMID:12589427
DOID:2377 multiple sclerosis HGNC:7884 Homo sapiens (human) 4855 NOTCH4 inference by association of genotype from phenotype used in manual assertion
  • PMID:21654846
DOID:418 systemic scleroderma HGNC:7884 Homo sapiens (human) 4855 NOTCH4 inference by association of genotype from phenotype used in manual assertion
  • PMID:21779181
DOID:5419 schizophrenia HGNC:7884 Homo sapiens (human) 4855 NOTCH4 inference by association of genotype from phenotype used in manual assertion
  • PMID:14732589
  • PMID:16894623
DOID:9744 type 1 diabetes mellitus HGNC:7884 Homo sapiens (human) 4855 NOTCH4 inference by association of genotype from phenotype used in manual assertion
  • PMID:19143814
DOID:653 purine-pyrimidine metabolic disorder HGNC:7892 Homo sapiens (human) 4860 PNP inference by association of genotype from phenotype used in manual assertion
  • PMID:3029074
DOID:5813 purine nucleoside phosphorylase deficiency HGNC:7892 Homo sapiens (human) 4860 PNP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070113 Niemann-Pick disease type C1 HGNC:7897 Homo sapiens (human) 4864 NPC1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2945 severe acute respiratory syndrome HGNC:79 Homo sapiens (human) 28 ABO inference by association of genotype from phenotype used in manual assertion
  • PMID:15784866
DOID:9952 acute lymphoblastic leukemia HGNC:79 Homo sapiens (human) 28 ABO inference by association of genotype from phenotype used in manual assertion
  • PMID:17065136

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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: April 7, 2025