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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 451 - 475 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:0111717 isolated cryptophthalmia MGI:2444465 Mus musculus (house mouse) 242022 Frem2 author statement supported by traceable reference
  • PMID:30802441
DOID:0060212 amyotrophic lateral sclerosis type 21 MGI:1298379 Mus musculus (house mouse) 17184 Matr3 author statement supported by traceable reference
  • PMID:33082323
DOID:0110964 brachydactyly type A1 MGI:96533 Mus musculus (house mouse) 16147 Ihh author statement supported by traceable reference
  • PMID:19252479
DOID:11166 Human papillomavirus infectious disease HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12918070
  • PMID:12941545
  • PMID:19272325
DOID:5409 lung small cell carcinoma HGNC:795 Homo sapiens (human) 472 ATM inference by association of genotype from phenotype used in manual assertion
  • PMID:28642860
DOID:0080124 mitochondrial DNA depletion syndrome 5 HGNC:11448 Homo sapiens (human) 8803 SUCLA2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1273 respiratory syncytial virus infectious disease HGNC:10802 Homo sapiens (human) 6440 SFTPC inference by association of genotype from phenotype used in manual assertion
  • PMID:17121584
DOID:0080066 autosomal recessive spinocerebellar ataxia 20 SGD:S000004572 Saccharomyces cerevisiae S288C 854867 MDM1 mutant phenotype evidence used in manual assertion
  • PMID:26283797
  • PMID:33740659
DOID:13189 gout HGNC:10931 Homo sapiens (human) 10786 SLC17A3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8472 localized scleroderma HGNC:7155 Homo sapiens (human) 4312 MMP1 direct assay evidence used in manual assertion
  • PMID:9804345
DOID:0111632 familial erythrocytosis 6 HGNC:4827 Homo sapiens (human) 3043 HBB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:13099 Moyamoya disease HGNC:14539 Homo sapiens (human) 57674 RNF213 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10591 pre-eclampsia HGNC:6149 Homo sapiens (human) 3684 ITGAM inference by association of genotype from phenotype used in manual assertion
  • PMID:33539617
DOID:0060291 oculodentodigital dysplasia MGI:95713 Mus musculus (house mouse) 14609 Gja1 author statement supported by traceable reference
  • PMID:16155213
  • PMID:17311295
  • PMID:18003637
  • PMID:18077386
DOID:0050908 myelodysplastic syndrome HGNC:18318 Homo sapiens (human) 171023 ASXL1 direct assay evidence used in manual assertion
  • PMID:23099237
DOID:0110734 neurodegeneration with brain iron accumulation HGNC:15578 Homo sapiens (human) 85021 REPS1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10584 retinitis pigmentosa HGNC:29253 Homo sapiens (human) 57545 CC2D2A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:83 cataract RGD:69062 Rattus norvegicus (Norway rat) 83571 Cdkn1b mutant phenotype evidence used in manual assertion
  • PMID:30893315
DOID:0050852 limb ischemia HGNC:4893 Homo sapiens (human) 3082 HGF direct assay evidence used in manual assertion
  • PMID:15238569
DOID:3393 coronary artery disease HGNC:288 Homo sapiens (human) 155 ADRB3 inference by association of genotype from phenotype used in manual assertion
  • PMID:9126344
DOID:4465 papillary renal cell carcinoma HGNC:7029 Homo sapiens (human) 4233 MET inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12361 Graves' disease HGNC:1142 Homo sapiens (human) 56244 BTNL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:24684463
DOID:3748 esophagus squamous cell carcinoma HGNC:25941 Homo sapiens (human) 54790 TET2 inference by association of genotype from phenotype used in manual assertion
  • PMID:26873401
DOID:0112376 muscular dystrophy-dystroglycanopathy type B15 HGNC:3007 Homo sapiens (human) 54344 DPM3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112266 nephrotic syndrome type 23 HGNC:15734 Homo sapiens (human) 55243 KIRREL1 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.

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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