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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 5826 - 5850 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence References
DOID:5520 head and neck squamous cell carcinoma HGNC:11904 Homo sapiens (human) 8797 TNFRSF10A inference by association of genotype from phenotype used in manual assertion
  • PMID:16217763
DOID:0050746 mantle cell lymphoma HGNC:11904 Homo sapiens (human) 8797 TNFRSF10A inference by association of genotype from phenotype used in manual assertion
  • PMID:15531454
  • PMID:16217763
DOID:4450 renal cell carcinoma HGNC:11904 Homo sapiens (human) 8797 TNFRSF10A mutant phenotype evidence used in manual assertion
  • PMID:17184908
DOID:11054 urinary bladder cancer HGNC:11904 Homo sapiens (human) 8797 TNFRSF10A inference by association of genotype from phenotype used in manual assertion
  • PMID:16217763
DOID:4914 esophagus adenocarcinoma HGNC:11904 Homo sapiens (human) 8797 TNFRSF10A inference by association of genotype from phenotype used in manual assertion
  • PMID:21472143
DOID:4362 cervical cancer HGNC:11904 Homo sapiens (human) 8797 TNFRSF10A mutant phenotype evidence used in manual assertion
  • PMID:16271751
DOID:9538 multiple myeloma HGNC:11904 Homo sapiens (human) 8797 TNFRSF10A direct assay evidence used in manual assertion
  • PMID:16531263
DOID:5520 head and neck squamous cell carcinoma HGNC:11905 Homo sapiens (human) 8795 TNFRSF10B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:5408 Paget's disease of bone HGNC:11908 Homo sapiens (human) 8792 TNFRSF11A inference by association of genotype from phenotype used in manual assertion
  • PMID:10615125
DOID:0111542 familial expansile osteolysis HGNC:11908 Homo sapiens (human) 8792 TNFRSF11A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080006 bone development disease HGNC:11908 Homo sapiens (human) 8792 TNFRSF11A inference by association of genotype from phenotype used in manual assertion
  • PMID:10615125
DOID:11476 osteoporosis HGNC:11908 Homo sapiens (human) 8792 TNFRSF11A inference by association of genotype from phenotype used in manual assertion
  • PMID:17002564
DOID:0081365 Paget's disease of bone 2 HGNC:11908 Homo sapiens (human) 8792 TNFRSF11A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110946 autosomal recessive osteopetrosis 7 HGNC:11908 Homo sapiens (human) 8792 TNFRSF11A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10908 hydrocephalus HGNC:7208 Homo sapiens (human) 8777 MPDZ inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:612 primary immunodeficiency disease HGNC:3573 Homo sapiens (human) 8772 FADD inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1240 leukemia HGNC:3573 Homo sapiens (human) 8772 FADD inference by association of genotype from phenotype used in manual assertion
  • PMID:22244917
DOID:0110587 autosomal dominant nonsyndromic deafness 66 HGNC:1632 Homo sapiens (human) 8763 CD164 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111020 cone-rod dystrophy 9 HGNC:216 Homo sapiens (human) 8754 ADAM9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080630 B-lymphoblastic leukemia/lymphoma HGNC:11928 Homo sapiens (human) 8741 TNFSF13 mutant phenotype evidence used in manual assertion
  • PMID:15488762
DOID:0111952 immunodeficiency 57 HGNC:10019 Homo sapiens (human) 8737 RIPK1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110202 Charcot-Marie-Tooth disease dominant intermediate A HGNC:4181 Homo sapiens (human) 8729 GBF1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110727 neuronal ceroid lipofuscinosis 13 HGNC:2531 Homo sapiens (human) 8722 CTSF inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112283 spondyloepiphyseal dysplasia Kondo-Fu type HGNC:15456 Homo sapiens (human) 8720 MBTPS1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2986 IgA glomerulonephritis HGNC:13902 Homo sapiens (human) 8710 SERPINB7 inference by association of genotype from phenotype used in manual assertion
  • PMID:16550745
  • PMID:16796905
  • PMID:18793525
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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