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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 2701 - 2725 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence References
DOID:3070 high grade glioma HGNC:10830 Homo sapiens (human) 6455 SH3GL1 direct assay evidence used in manual assertion
  • PMID:23050879
DOID:9119 acute myeloid leukemia HGNC:10830 Homo sapiens (human) 6455 SH3GL1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1856 cherubism HGNC:10825 Homo sapiens (human) 6452 SH3BP2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11381256
  • RGD:7240710
DOID:0060705 X-linked lymphoproliferative syndrome 1 HGNC:10820 Homo sapiens (human) 4068 SH2D1A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12801 mucopolysaccharidosis III HGNC:10818 Homo sapiens (human) 6448 SGSH inference by association of genotype from phenotype used in manual assertion
  • PMID:15902564
DOID:0111395 mucopolysaccharidosis type IIIA HGNC:10818 Homo sapiens (human) 6448 SGSH inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080265 nephrotic syndrome type 14 HGNC:10817 Homo sapiens (human) 8879 SGPL1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080721 calvarial doughnut lesions with bone fragility HGNC:28395 Homo sapiens (human) 166929 SGMS2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8947 diabetic retinopathy HGNC:25156 Homo sapiens (human) 112869 SGF29 inference by association of genotype from phenotype used in manual assertion
  • PMID:21441570
DOID:0110277 autosomal recessive limb-girdle muscular dystrophy type 2C HGNC:10809 Homo sapiens (human) 6445 SGCG inference by association of genotype from phenotype used in manual assertion
  • PMID:25802879
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:10809 Homo sapiens (human) 6445 SGCG inference by association of genotype from phenotype used in manual assertion
  • PMID:28123479
DOID:0090034 myoclonic dystonia 11 HGNC:10808 Homo sapiens (human) 8910 SGCE inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9884 muscular dystrophy HGNC:10807 Homo sapiens (human) 6444 SGCD inference by association of genotype from phenotype used in manual assertion
  • PMID:8841194
DOID:0110436 dilated cardiomyopathy 1L HGNC:10807 Homo sapiens (human) 6444 SGCD inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110280 autosomal recessive limb-girdle muscular dystrophy type 2F HGNC:10807 Homo sapiens (human) 6444 SGCD inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110279 autosomal recessive limb-girdle muscular dystrophy type 2E HGNC:10806 Homo sapiens (human) 6443 SGCB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110279 autosomal recessive limb-girdle muscular dystrophy type 2E HGNC:10806 Homo sapiens (human) 6443 SGCB direct assay evidence used in manual assertion
  • PMID:28284983
DOID:9884 muscular dystrophy HGNC:10806 Homo sapiens (human) 6443 SGCB inference by association of genotype from phenotype used in manual assertion
  • PMID:9631401
DOID:9884 muscular dystrophy HGNC:10805 Homo sapiens (human) 6442 SGCA inference by association of genotype from phenotype used in manual assertion
  • PMID:8069911
  • PMID:9192266
DOID:0110278 autosomal recessive limb-girdle muscular dystrophy type 2D HGNC:10805 Homo sapiens (human) 6442 SGCA direct assay evidence used in manual assertion
  • PMID:17653106
DOID:0110278 autosomal recessive limb-girdle muscular dystrophy type 2D HGNC:10805 Homo sapiens (human) 6442 SGCA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12716 newborn respiratory distress syndrome HGNC:10803 Homo sapiens (human) 6441 SFTPD inference by association of genotype from phenotype used in manual assertion
  • PMID:17524024
DOID:3083 chronic obstructive pulmonary disease HGNC:10803 Homo sapiens (human) 6441 SFTPD direct assay evidence used in manual assertion
  • PMID:18310480
DOID:3908 lung non-small cell carcinoma HGNC:10803 Homo sapiens (human) 6441 SFTPD direct assay evidence used in manual assertion
  • PMID:20401612
DOID:1273 respiratory syncytial virus infectious disease HGNC:10803 Homo sapiens (human) 6441 SFTPD inference by association of genotype from phenotype used in manual assertion
  • PMID:19287351
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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