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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 5951 - 5975 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:4886 Homo sapiens (human) 3077 HFE inference by association of genotype from phenotype used in manual assertion
  • PMID:14973098
DOID:1184 nephrotic syndrome HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:14758530
DOID:0110477 autosomal recessive nonsyndromic deafness 2 HGNC:7606 Homo sapiens (human) 4647 MYO7A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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:0110313 hypertrophic cardiomyopathy 7 HGNC:11947 Homo sapiens (human) 7137 TNNI3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11054 urinary bladder cancer HGNC:2623 Homo sapiens (human) 1559 CYP2C9 inference by association of genotype from phenotype used in manual assertion
  • PMID:16985032
DOID:4947 cholangiocarcinoma HGNC:583 Homo sapiens (human) 324 APC inference by association of genotype from phenotype used in manual assertion
  • PMID:10212000
DOID:10003 sensorineural hearing loss HGNC:4172 Homo sapiens (human) 2625 GATA3 inference by association of genotype from phenotype used in manual assertion
  • PMID:10935639
DOID:0060751 familial temporal lobe epilepsy 7 HGNC:9957 Homo sapiens (human) 5649 RELN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050452 mevalonic aciduria HGNC:7530 Homo sapiens (human) 4598 MVK inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9538 multiple myeloma HGNC:4886 Homo sapiens (human) 3077 HFE inference by association of genotype from phenotype used in manual assertion
  • PMID:10383894
DOID:8778 Crohn's disease HGNC:10720 Homo sapiens (human) 6402 SELL inference by association of genotype from phenotype used in manual assertion
  • PMID:19212205
DOID:10976 membranous glomerulonephritis HGNC:7154 Homo sapiens (human) 4311 MME inference by association of genotype from phenotype used in manual assertion
  • PMID:15464186
DOID:8947 diabetic retinopathy HGNC:4886 Homo sapiens (human) 3077 HFE inference by association of genotype from phenotype used in manual assertion
  • PMID:15347835
DOID:0110014 age related macular degeneration 1 HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:526 human immunodeficiency virus infectious disease HGNC:40 Homo sapiens (human) 5243 ABCB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:23133441
DOID:0050742 nicotine dependence HGNC:3023 Homo sapiens (human) 1813 DRD2 inference by association of genotype from phenotype used in manual assertion
  • PMID:17085484
  • PMID:17108814
  • PMID:17654295
  • PMID:22382052
DOID:251 alcohol-induced mental disorder HGNC:3023 Homo sapiens (human) 1813 DRD2 inference by association of genotype from phenotype used in manual assertion
  • PMID:18669994
DOID:10283 prostate cancer HGNC:9605 Homo sapiens (human) 5743 PTGS2 inference by association of genotype from phenotype used in manual assertion
  • PMID:26788504
DOID:0080630 B-lymphoblastic leukemia/lymphoma HGNC:13176 Homo sapiens (human) 10320 IKZF1 inference by association of genotype from phenotype used in manual assertion
  • PMID:22699455
DOID:10923 sickle cell anemia HGNC:13221 Homo sapiens (human) 53335 BCL11A inference by association of genotype from phenotype used in manual assertion
  • PMID:18667698
DOID:0050657 Bannayan-Riley-Ruvalcaba syndrome HGNC:9588 Homo sapiens (human) 5728 PTEN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080387 nephrotic syndrome type 12 HGNC:28958 Homo sapiens (human) 9688 NUP93 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12930 dilated cardiomyopathy HGNC:9393 Homo sapiens (human) 5578 PRKCA inference by association of genotype from phenotype used in manual assertion
  • PMID:9918525
DOID:0070600 intellectual disability and myopathy syndrome HGNC:60 Homo sapiens (human) 10060 ABCC9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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International Collaboration

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