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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 10026 - 10050 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence References
DOID:162 cancer SGD:S000000605 Saccharomyces cerevisiae S288C 850370 PGK1 sequence similarity evidence used in manual assertion
  • PMID:26354769
DOID:0080570 congenital disorder of glycosylation It HGNC:8905 Homo sapiens (human) 5236 PGM1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080570 congenital disorder of glycosylation It SGD:S000001610 Saccharomyces cerevisiae S288C 853732 PGM1 genetic interaction evidence used in manual assertion
  • PMID:38743592
DOID:1380 endometrial cancer HGNC:8905 Homo sapiens (human) 5236 PGM1 inference by association of genotype from phenotype used in manual assertion
  • PMID:508567
DOID:0080570 congenital disorder of glycosylation It SGD:S000001610 Saccharomyces cerevisiae S288C 853732 PGM1 sequence similarity evidence used in manual assertion
  • PMID:38743592
DOID:3307 teratoma HGNC:8905 Homo sapiens (human) 5236 PGM1 inference by association of genotype from phenotype used in manual assertion
  • PMID:5259759
DOID:0080570 congenital disorder of glycosylation It SGD:S000004711 Saccharomyces cerevisiae S288C 855131 PGM2 sequence similarity evidence used in manual assertion
  • PMID:38743592
DOID:0080570 congenital disorder of glycosylation It SGD:S000004711 Saccharomyces cerevisiae S288C 855131 PGM2 genetic interaction evidence used in manual assertion
  • PMID:38743592
DOID:0111953 immunodeficiency 23 HGNC:8907 Homo sapiens (human) 5238 PGM3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3307 teratoma HGNC:8907 Homo sapiens (human) 5238 PGM3 inference by association of genotype from phenotype used in manual assertion
  • PMID:5259759
DOID:12700 hyperprolactinemia HGNC:8910 Homo sapiens (human) 5241 PGR inference by association of genotype from phenotype used in manual assertion
  • PMID:15807882
DOID:9970 obesity HGNC:8910 Homo sapiens (human) 5241 PGR inference by association of genotype from phenotype used in manual assertion
  • PMID:14557830
DOID:289 endometriosis HGNC:8910 Homo sapiens (human) 5241 PGR inference by association of genotype from phenotype used in manual assertion
  • PMID:16126772
DOID:0050161 lower respiratory tract disease FB:FBgn0035976 Drosophila melanogaster (fruit fly) 39063 PGRP-LC CG4432 combinatorial experimental and author inference evidence used in manual assertion
  • PMID:33826881
DOID:0050161 lower respiratory tract disease FB:FBgn0030695 Drosophila melanogaster (fruit fly) 32534 PGRP-LE CG8995 combinatorial experimental and author inference evidence used in manual assertion
  • PMID:33826881
DOID:14330 Parkinson's disease HGNC:20956 Homo sapiens (human) 9749 PHACTR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:19429005
DOID:2377 multiple sclerosis HGNC:20956 Homo sapiens (human) 9749 PHACTR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:20546594
DOID:8029 sporadic breast cancer HGNC:8912 Homo sapiens (human) 5245 PHB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:1540973
DOID:1612 breast cancer HGNC:8912 Homo sapiens (human) 5245 PHB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11377649
  • RGD:7240710
DOID:0070287 primary autosomal recessive microcephaly 11 HGNC:3182 Homo sapiens (human) 1911 PHC1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050445 X-linked hypophosphatemic rickets HGNC:8918 Homo sapiens (human) 5251 PHEX inference by association of genotype from phenotype used in manual assertion
  • PMID:7550339
  • PMID:9106524
  • RGD:7240710
DOID:6000 congestive heart failure HGNC:18145 Homo sapiens (human) 84295 PHF6 inference by association of genotype from phenotype used in manual assertion
  • PMID:33779075
DOID:0050681 Borjeson-Forssman-Lehmann syndrome HGNC:18145 Homo sapiens (human) 84295 PHF6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9119 acute myeloid leukemia HGNC:18145 Homo sapiens (human) 84295 PHF6 inference by association of genotype from phenotype used in manual assertion
  • PMID:31186809
DOID:0060812 syndromic X-linked intellectual disability Siderius type HGNC:20672 Homo sapiens (human) 23133 PHF8 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