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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 5801 - 5825 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:5844 myocardial infarction RGD:2993 Rattus norvegicus (Norway rat) 24530 Lcat direct assay evidence used in manual assertion
  • PMID:16640830
DOID:2590 familial nephrotic syndrome HGNC:18143 Homo sapiens (human) 23500 DAAM2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1115 sarcoma HGNC:6973 Homo sapiens (human) 4193 MDM2 inference by association of genotype from phenotype used in manual assertion
  • PMID:1614537
DOID:5176 renal Wilms' tumor HGNC:10524 Homo sapiens (human) 6299 SALL1 mutant phenotype evidence used in manual assertion
  • PMID:18467665
DOID:783 end stage renal disease HGNC:4323 Homo sapiens (human) 2739 GLO1 inference by association of genotype from phenotype used in manual assertion
  • PMID:20185929
DOID:0110527 autosomal recessive nonsyndromic deafness 8 HGNC:11877 Homo sapiens (human) 64699 TMPRSS3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112310 central precocious puberty 1 HGNC:4510 Homo sapiens (human) 84634 KISS1R inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110731 neuronal ceroid lipofuscinosis 3 MGI:103555 Mus musculus (house mouse) 12725 Clcn3 author statement supported by traceable reference
  • PMID:12059962
DOID:0080735 Ehlers-Danlos syndrome kyphoscoliotic type 2 HGNC:18625 Homo sapiens (human) 55033 FKBP14 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080441 developmental and epileptic encephalopathy 49 HGNC:19344 Homo sapiens (human) 23258 DENND5A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:303 substance-related disorder RGD:70982 Rattus norvegicus (Norway rat) 84027 Gsk3b mutant phenotype evidence used in manual assertion
  • PMID:30188517
DOID:1686 glaucoma HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10511023
DOID:4450 renal cell carcinoma HGNC:7173 Homo sapiens (human) 4314 MMP3 inference by association of genotype from phenotype used in manual assertion
  • PMID:15319295
  • PMID:19551141
DOID:0060903 thrombosis RGD:621681 Rattus norvegicus (Norway rat) 64803 P2ry12 mutant phenotype evidence used in manual assertion
  • PMID:19692114
DOID:446 primary hyperaldosteronism HGNC:2592 Homo sapiens (human) 1585 CYP11B2 inference by association of genotype from phenotype used in manual assertion
  • PMID:1731223
DOID:0080139 multiple congenital anomalies-hypotonia-seizures syndrome 2 HGNC:8957 Homo sapiens (human) 5277 PIGA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9111 cutaneous leishmaniasis HGNC:1606 Homo sapiens (human) 1234 CCR5 inference by association of genotype from phenotype used in manual assertion
  • PMID:23632983
DOID:2339 Crouzon syndrome MGI:95523 Mus musculus (house mouse) 14183 Fgfr2 author statement supported by traceable reference
  • PMID:15316116
  • PMID:17132737
  • PMID:20503384
  • PMID:25966306
DOID:3827 congenital diaphragmatic hernia MGI:2670972 Mus musculus (house mouse) 329872 Frem1 author statement supported by traceable reference
  • PMID:23221805
DOID:684 hepatocellular carcinoma HGNC:15633 Homo sapiens (human) 54106 TLR9 mutant phenotype evidence used in manual assertion
  • PMID:24452201
DOID:0111532 osteoglophonic dysplasia HGNC:3688 Homo sapiens (human) 2260 FGFR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15625620
  • RGD:7240710
DOID:783 end stage renal disease HGNC:6156 Homo sapiens (human) 3690 ITGB3 inference by association of genotype from phenotype used in manual assertion
  • PMID:19368146
DOID:1909 melanoma HGNC:11919 Homo sapiens (human) 958 CD40 mutant phenotype evidence used in manual assertion
  • PMID:17327609
DOID:0060611 abdominal obesity-metabolic syndrome MGI:97747 Mus musculus (house mouse) 19016 Pparg author statement supported by traceable reference
  • PMID:15716267
DOID:3132 porphyria cutanea tarda HGNC:2595 Homo sapiens (human) 1543 CYP1A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:14714565
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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: December 8, 2025