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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 10076 - 10100 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:1612 breast cancer HGNC:795 Homo sapiens (human) 472 ATM inference by association of genotype from phenotype used in manual assertion
  • PMID:11200774
  • RGD:7240710
DOID:5409 lung small cell carcinoma HGNC:795 Homo sapiens (human) 472 ATM inference by association of genotype from phenotype used in manual assertion
  • PMID:28642860
DOID:1380 endometrial cancer HGNC:795 Homo sapiens (human) 472 ATM inference by association of genotype from phenotype used in manual assertion
  • PMID:17164260
DOID:12704 ataxia telangiectasia HGNC:795 Homo sapiens (human) 472 ATM inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1441 autosomal dominant cerebellar ataxia HGNC:7952 Homo sapiens (human) 4884 NPTX1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050742 nicotine dependence HGNC:7956 Homo sapiens (human) 4886 NPY1R inference by association of genotype from phenotype used in manual assertion
  • PMID:22309839
DOID:809 cocaine abuse HGNC:7956 Homo sapiens (human) 4886 NPY1R inference by association of genotype from phenotype used in manual assertion
  • PMID:33242852
DOID:2559 opiate dependence HGNC:7956 Homo sapiens (human) 4886 NPY1R inference by association of genotype from phenotype used in manual assertion
  • PMID:31689297
  • PMID:32757697
DOID:9976 heroin dependence HGNC:7956 Homo sapiens (human) 4886 NPY1R inference by association of genotype from phenotype used in manual assertion
  • PMID:24845178
  • PMID:29465008
DOID:670 amphetamine abuse HGNC:7956 Homo sapiens (human) 4886 NPY1R inference by association of genotype from phenotype used in manual assertion
  • PMID:19566775
DOID:11981 morbid obesity HGNC:7957 Homo sapiens (human) 4887 NPY2R inference by association of genotype from phenotype used in manual assertion
  • PMID:15855352
DOID:12858 Huntington's disease HGNC:7957 Homo sapiens (human) 4887 NPY2R inference by association of genotype from phenotype used in manual assertion
  • PMID:24121255
DOID:9970 obesity HGNC:7957 Homo sapiens (human) 4887 NPY2R inference by association of genotype from phenotype used in manual assertion
  • PMID:17019604
DOID:9970 obesity HGNC:7958 Homo sapiens (human) 4889 NPY5R inference by association of genotype from phenotype used in manual assertion
  • PMID:10849579
  • PMID:23900445
DOID:3146 lipid metabolism disorder HGNC:7958 Homo sapiens (human) 4889 NPY5R inference by association of genotype from phenotype used in manual assertion
  • PMID:17426313
DOID:0080156 X-linked adrenal hypoplasia congenita HGNC:7960 Homo sapiens (human) 190 NR0B1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111777 46,XY sex reversal 2 HGNC:7960 Homo sapiens (human) 190 NR0B1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112313 brain small vessel disease HGNC:7962 Homo sapiens (human) 9572 NR1D1 inference by association of genotype from phenotype used in manual assertion
  • PMID:23083441
DOID:5844 myocardial infarction HGNC:7966 Homo sapiens (human) 10062 NR1H3 inference by association of genotype from phenotype used in manual assertion
  • PMID:21903943
DOID:6713 cerebrovascular disease HGNC:7966 Homo sapiens (human) 10062 NR1H3 inference by association of genotype from phenotype used in manual assertion
  • PMID:21903943
DOID:9970 obesity HGNC:7966 Homo sapiens (human) 10062 NR1H3 inference by association of genotype from phenotype used in manual assertion
  • PMID:17108812
DOID:3526 cerebral infarction HGNC:7966 Homo sapiens (human) 10062 NR1H3 inference by association of genotype from phenotype used in manual assertion
  • PMID:21903943
DOID:0110399 retinitis pigmentosa 37 HGNC:7974 Homo sapiens (human) 10002 NR2E3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0090059 enhanced S-cone syndrome HGNC:7974 Homo sapiens (human) 10002 NR2E3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080943 46,XX sex reversal 5 HGNC:7976 Homo sapiens (human) 7026 NR2F2 inference by association of genotype from phenotype used in manual assertion
  • 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: April 7, 2025