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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 5926 - 5950 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence References
DOID:0080240 non-syndromic X-linked intellectual disability 106 HGNC:8127 Homo sapiens (human) 8473 OGT inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111835 congenital nongoitrous hypothyroidism 9 HGNC:6128 Homo sapiens (human) 8471 IRS4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1324 lung cancer HGNC:6128 Homo sapiens (human) 8471 IRS4 mutant phenotype evidence used in manual assertion
  • PMID:33894221
DOID:0050861 colorectal adenocarcinoma HGNC:12020 Homo sapiens (human) 8460 TPST1 inference by association of genotype from phenotype used in manual assertion
  • PMID:27354594
DOID:4479 pseudohypoaldosteronism HGNC:2553 Homo sapiens (human) 8452 CUL3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060822 syndromic X-linked intellectual disability Cabezas type HGNC:2555 Homo sapiens (human) 8450 CUL4B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110852 rhizomelic chondrodysplasia punctata type 2 HGNC:4416 Homo sapiens (human) 8443 GNPAT inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:11178 Homo sapiens (human) 8435 SOAT2 direct assay evidence used in manual assertion
  • PMID:16274362
DOID:3393 coronary artery disease HGNC:11178 Homo sapiens (human) 8435 SOAT2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16195894
DOID:0070139 autosomal recessive cutis laxa type IC HGNC:6717 Homo sapiens (human) 8425 LTBP4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9256 colorectal cancer HGNC:11254 Homo sapiens (human) 8405 SPOP direct assay evidence used in manual assertion
  • PMID:28032859
DOID:3910 lung adenocarcinoma HGNC:11254 Homo sapiens (human) 8405 SPOP mutant phenotype evidence used in manual assertion
  • PMID:30607139
DOID:684 hepatocellular carcinoma HGNC:11254 Homo sapiens (human) 8405 SPOP mutant phenotype evidence used in manual assertion
  • PMID:33209975
DOID:0050773 paraganglioma HGNC:10981 Homo sapiens (human) 8402 SLC25A11 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:9039 Homo sapiens (human) 8398 PLA2G6 inference by association of genotype from phenotype used in manual assertion
  • PMID:20938027
DOID:0110735 neurodegeneration with brain iron accumulation 2a HGNC:9039 Homo sapiens (human) 8398 PLA2G6 inference by association of genotype from phenotype used in manual assertion
  • PMID:22934738
  • RGD:7240710
DOID:0110736 neurodegeneration with brain iron accumulation 2b HGNC:9039 Homo sapiens (human) 8398 PLA2G6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0090056 dystonia 12 HGNC:9039 Homo sapiens (human) 8398 PLA2G6 inference by association of genotype from phenotype used in manual assertion
  • PMID:19087156
DOID:2367 neuroaxonal dystrophy HGNC:9039 Homo sapiens (human) 8398 PLA2G6 inference by association of genotype from phenotype used in manual assertion
  • PMID:17033970
  • PMID:19138334
DOID:0060900 Parkinson's disease 14 HGNC:9039 Homo sapiens (human) 8398 PLA2G6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080079 nonsyndromic congenital nail disorder 1 HGNC:4044 Homo sapiens (human) 8323 FZD6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111412 exudative vitreoretinopathy 1 HGNC:4042 Homo sapiens (human) 8322 FZD4 inference by association of genotype from phenotype used in manual assertion
  • PMID:12172548
  • RGD:7240710
DOID:3495 extrahepatic bile duct adenocarcinoma HGNC:950 Homo sapiens (human) 8314 BAP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:25536104
DOID:6039 uveal melanoma HGNC:950 Homo sapiens (human) 8314 BAP1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2513 basal cell carcinoma HGNC:950 Homo sapiens (human) 8314 BAP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:25080371
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International Collaboration

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