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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 9951 - 9975 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence References
DOID:4586 familial meningioma HGNC:8800 Homo sapiens (human) 5155 PDGFB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3070 high grade glioma HGNC:8800 Homo sapiens (human) 5155 PDGFB mutant phenotype evidence used in manual assertion
  • PMID:21677873
  • PMID:26945107
DOID:3068 glioblastoma HGNC:8800 Homo sapiens (human) 5155 PDGFB mutant phenotype evidence used in manual assertion
  • PMID:21210235
DOID:3507 dermatofibrosarcoma protuberans HGNC:8800 Homo sapiens (human) 5155 PDGFB inference by association of genotype from phenotype used in manual assertion
  • PMID:12641779
  • RGD:7240710
DOID:11132 prostatic hypertrophy HGNC:30620 Homo sapiens (human) 80310 PDGFD mutant phenotype evidence used in manual assertion
  • PMID:22689130
DOID:999 hypereosinophilic syndrome HGNC:8803 Homo sapiens (human) 5156 PDGFRA inference by association of genotype from phenotype used in manual assertion
  • PMID:12660384
  • RGD:7240710
DOID:1793 pancreatic cancer HGNC:8803 Homo sapiens (human) 5156 PDGFRA mutant phenotype evidence used in manual assertion
  • PMID:14695158
DOID:1240 leukemia HGNC:8803 Homo sapiens (human) 5156 PDGFRA mutant phenotype evidence used in manual assertion
  • PMID:21224473
DOID:8683 myeloid sarcoma HGNC:8803 Homo sapiens (human) 5156 PDGFRA mutant phenotype evidence used in manual assertion
  • PMID:22348015
DOID:8692 myeloid leukemia HGNC:8803 Homo sapiens (human) 5156 PDGFRA mutant phenotype evidence used in manual assertion
  • PMID:24486648
DOID:5603 T-cell acute lymphoblastic leukemia HGNC:8803 Homo sapiens (human) 5156 PDGFRA mutant phenotype evidence used in manual assertion
  • PMID:24486648
DOID:0060230 basal ganglia calcification HGNC:8804 Homo sapiens (human) 5159 PDGFRB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:4450 renal cell carcinoma HGNC:8804 Homo sapiens (human) 5159 PDGFRB mutant phenotype evidence used in manual assertion
  • PMID:15994946
DOID:3068 glioblastoma HGNC:8804 Homo sapiens (human) 5159 PDGFRB mutant phenotype evidence used in manual assertion
  • PMID:24566984
DOID:0111344 myeloproliferative disorder with eosinophilia HGNC:8804 Homo sapiens (human) 5159 PDGFRB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2226 myeloproliferative neoplasm HGNC:8804 Homo sapiens (human) 5159 PDGFRB inference by association of genotype from phenotype used in manual assertion
  • PMID:12181402
DOID:0080109 infantile myofibromatosis HGNC:8804 Homo sapiens (human) 5159 PDGFRB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9256 colorectal cancer HGNC:8805 Homo sapiens (human) 5157 PDGFRL inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:8805 Homo sapiens (human) 5157 PDGFRL inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3649 pyruvate decarboxylase deficiency HGNC:8806 Homo sapiens (human) 5160 PDHA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10679936
  • PMID:20002461
  • RGD:7240710
DOID:0070569 spermatogenic failure 70 HGNC:8807 Homo sapiens (human) 5161 PDHA2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3649 pyruvate decarboxylase deficiency HGNC:8808 Homo sapiens (human) 5162 PDHB inference by association of genotype from phenotype used in manual assertion
  • PMID:15138885
  • RGD:7240710
DOID:1115 sarcoma HGNC:21350 Homo sapiens (human) 8050 PDHX inference by association of genotype from phenotype used in manual assertion
  • PMID:31089155
DOID:3649 pyruvate decarboxylase deficiency HGNC:21350 Homo sapiens (human) 8050 PDHX inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2048 autoimmune hepatitis HGNC:4606 Homo sapiens (human) 2923 PDIA3 direct assay evidence used in manual assertion
  • PMID:20208391
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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