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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 9876 - 9900 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence References
DOID:1793 pancreatic cancer HGNC:17068 Homo sapiens (human) 23022 PALLD inference by association of genotype from phenotype used in manual assertion
  • PMID:17194196
  • RGD:7240710
DOID:3981 pantothenate kinase-associated neurodegeneration HGNC:15894 Homo sapiens (human) 80025 PANK2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1596 depressive disorder HGNC:8599 Homo sapiens (human) 24145 PANX1 inference by association of genotype from phenotype used in manual assertion
  • PMID:35642741
DOID:5844 myocardial infarction HGNC:8602 Homo sapiens (human) 5069 PAPPA inference by association of genotype from phenotype used in manual assertion
  • PMID:17700210
DOID:0050812 spondyloepimetaphyseal dysplasia, Pakistani type HGNC:8604 Homo sapiens (human) 9060 PAPSS2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:16369 Homo sapiens (human) 11315 PARK7 inference by association of genotype from phenotype used in manual assertion
  • PMID:12851414
  • PMID:23766857
DOID:0080855 Parkinsonism HGNC:16369 Homo sapiens (human) 11315 PARK7 mutant phenotype evidence used in manual assertion
  • PMID:16860563
DOID:0060370 Parkinson's disease 7 HGNC:16369 Homo sapiens (human) 11315 PARK7 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3525 middle cerebral artery infarction HGNC:16369 Homo sapiens (human) 11315 PARK7 direct assay evidence used in manual assertion
  • PMID:17882163
DOID:3526 cerebral infarction HGNC:16369 Homo sapiens (human) 11315 PARK7 mutant phenotype evidence used in manual assertion
  • PMID:18003894
DOID:0070024 autosomal recessive dyskeratosis congenita 6 HGNC:8609 Homo sapiens (human) 5073 PARN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:270 Homo sapiens (human) 142 PARP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17290104
  • PMID:20486200
DOID:14330 Parkinson's disease HGNC:270 Homo sapiens (human) 142 PARP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17362997
DOID:2841 asthma HGNC:270 Homo sapiens (human) 142 PARP1 direct assay evidence used in manual assertion
  • PMID:26205779
DOID:9470 bacterial meningitis HGNC:270 Homo sapiens (human) 142 PARP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21651918
DOID:848 arthritis HGNC:270 Homo sapiens (human) 142 PARP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16461442
DOID:5517 stomach carcinoma HGNC:270 Homo sapiens (human) 142 PARP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18716896
DOID:10952 nephritis HGNC:270 Homo sapiens (human) 142 PARP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16461442
DOID:417 autoimmune disease HGNC:270 Homo sapiens (human) 142 PARP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16026592
DOID:0111132 focal segmental glomerulosclerosis 7 HGNC:8616 Homo sapiens (human) 5076 PAX2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:5176 renal Wilms' tumor HGNC:8616 Homo sapiens (human) 5076 PAX2 mutant phenotype evidence used in manual assertion
  • PMID:18467665
DOID:0090006 renal coloboma syndrome HGNC:8616 Homo sapiens (human) 5076 PAX2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070124 congenital nongoitrous hypothyroidism 2 HGNC:8622 Homo sapiens (human) 7849 PAX8 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050328 congenital hypothyroidism HGNC:8622 Homo sapiens (human) 7849 PAX8 inference by association of genotype from phenotype used in manual assertion
  • PMID:9590296
DOID:4450 renal cell carcinoma HGNC:30064 Homo sapiens (human) 55193 PBRM1 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