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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 14076 - 14100 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:6844 Homo sapiens (human) 6416 MAP2K4 inference by association of genotype from phenotype used in manual assertion
  • PMID:18772397
DOID:13963 nuclear senile cataract HGNC:24678 Homo sapiens (human) 79068 FTO inference by association of genotype from phenotype used in manual assertion
  • PMID:19329528
DOID:0050450 Gitelman syndrome HGNC:10912 Homo sapiens (human) 6559 SLC12A3 inference by association of genotype from phenotype used in manual assertion
  • PMID:16221718
  • RGD:7240710
DOID:10581 metachromatic leukodystrophy MGI:97783 Mus musculus (house mouse) 19156 Psap author statement supported by traceable reference
  • PMID:18480170
DOID:2316 brain ischemia HGNC:5233 Homo sapiens (human) 3304 HSPA1B inference by association of genotype from phenotype used in manual assertion
  • PMID:15992611
DOID:9352 type 2 diabetes mellitus HGNC:1391 Homo sapiens (human) 776 CACNA1D inference by association of genotype from phenotype used in manual assertion
  • PMID:23229155
DOID:0090107 autosomal dominant hypocalcemia 1 HGNC:1514 Homo sapiens (human) 846 CASR inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3969 papillary thyroid carcinoma HGNC:5173 Homo sapiens (human) 3265 HRAS inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111732 Eiken syndrome HGNC:9608 Homo sapiens (human) 5745 PTH1R inference by association of genotype from phenotype used in manual assertion
  • PMID:15525660
  • RGD:7240710
DOID:0050554 X-linked sideroblastic anemia with ataxia HGNC:48 Homo sapiens (human) 22 ABCB7 inference by association of genotype from phenotype used in manual assertion
  • PMID:10196363
  • PMID:11050011
  • PMID:11843825
  • RGD:7240710
DOID:12930 dilated cardiomyopathy MGI:1914502 Mus musculus (house mouse) 67252 Cap2 author statement supported by traceable reference
  • PMID:22945801
DOID:2377 multiple sclerosis MGI:104798 Mus musculus (house mouse) 21926 Tnf author statement supported by traceable reference
  • PMID:9736029
DOID:0090030 corticosteroid-binding globulin deficiency MGI:88278 Mus musculus (house mouse) 12401 Serpina6 author statement supported by traceable reference
  • PMID:16980625
  • PMID:20022933
  • PMID:22930537
DOID:1883 hepatitis C HGNC:6014 Homo sapiens (human) 3565 IL4 inference by association of genotype from phenotype used in manual assertion
  • PMID:28368861
DOID:0050561 Lennox-Gastaut syndrome MGI:2138334 Mus musculus (house mouse) 227333 Dgkd author statement supported by traceable reference
  • PMID:17357084
DOID:9970 obesity HGNC:7978 Homo sapiens (human) 2908 NR3C1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18246526
DOID:1612 breast cancer HGNC:10062 Homo sapiens (human) 56254 RNF20 direct assay evidence used in manual assertion
  • PMID:18832071
DOID:4440 seminoma SGD:S000002889 Saccharomyces cerevisiae S288C 852092 PHO8 sequence similarity evidence used in manual assertion
  • PMID:25860149
DOID:2841 asthma HGNC:11850 Homo sapiens (human) 7099 TLR4 inference by association of genotype from phenotype used in manual assertion
  • PMID:15356557
  • PMID:16266379
  • PMID:20685742
DOID:0090110 immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome MGI:1891436 Mus musculus (house mouse) 20371 Foxp3 author statement supported by traceable reference
  • PMID:11137992
  • PMID:19661482
DOID:1073 renal hypertension HGNC:7939 Homo sapiens (human) 4878 NPPA direct assay evidence used in manual assertion
  • PMID:15241786
DOID:1925 Coffin-Siris syndrome MGI:1935147 Mus musculus (house mouse) 93760 Arid1a author statement supported by traceable reference
  • PMID:26806701
DOID:65 connective tissue disease HGNC:11157 Homo sapiens (human) 6631 SNRPC direct assay evidence used in manual assertion
  • PMID:2968364
DOID:13141 uveitis RGD:621237 Rattus norvegicus (Norway rat) 25625 Tnfrsf1a mutant phenotype evidence used in manual assertion
  • PMID:12824249
DOID:9970 obesity RGD:3017 Rattus norvegicus (Norway rat) 24539 Lpl direct assay evidence used in manual assertion
  • PMID:27160499
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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 8, 2025