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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 13626 - 13650 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▼ Evidence References
DOID:12716 newborn respiratory distress syndrome HGNC:10801 Homo sapiens (human) 6439 SFTPB direct assay evidence used in manual assertion
  • PMID:12490037
DOID:0070538 syndromic X-linked intellectual developmental disorder bain type MGI:1201779 Mus musculus (house mouse) 56258 Hnrnph2 author statement supported by traceable reference
  • PMID:37463454
DOID:0050773 paraganglioma HGNC:26034 Homo sapiens (human) 54949 SDHAF2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080789 Treacher Collins syndrome 1 HGNC:11654 Homo sapiens (human) 6949 TCOF1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9675 pulmonary emphysema MGI:1101771 Mus musculus (house mouse) 16591 Kl author statement supported by traceable reference
  • PMID:9363890
DOID:10763 hypertension RGD:620217 Rattus norvegicus (Norway rat) 64522 Slc5a2 direct assay evidence used in manual assertion
  • PMID:14506074
DOID:5082 liver cirrhosis HGNC:10632 Homo sapiens (human) 6352 CCL5 inference by association of genotype from phenotype used in manual assertion
  • PMID:20978355
DOID:4195 hyperglycemia RGD:3001 Rattus norvegicus (Norway rat) 24536 Lepr mutant phenotype evidence used in manual assertion
  • PMID:26537785
DOID:10763 hypertension RGD:620630 Rattus norvegicus (Norway rat) 85268 Hrh3 direct assay evidence used in manual assertion
  • PMID:9050021
DOID:0080403 orofacial cleft 10 HGNC:12502 Homo sapiens (human) 7341 SUMO1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:11180 Homo sapiens (human) 6648 SOD2 direct assay evidence used in manual assertion
  • PMID:15094225
DOID:0111094 Fanconi anemia complementation group N HGNC:26144 Homo sapiens (human) 79728 PALB2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050811 congenital adrenal hyperplasia HGNC:2591 Homo sapiens (human) 1584 CYP11B1 inference by association of genotype from phenotype used in manual assertion
  • PMID:1430088
  • PMID:8964882
DOID:0111161 Crouzon syndrome-acanthosis nigricans syndrome HGNC:3690 Homo sapiens (human) 2261 FGFR3 inference by association of genotype from phenotype used in manual assertion
  • PMID:7493034
  • RGD:7240710
DOID:9256 colorectal cancer HGNC:3595 Homo sapiens (human) 2195 FAT1 inference by association of genotype from phenotype used in manual assertion
  • PMID:33106877
DOID:12554 hemolytic-uremic syndrome HGNC:24338 Homo sapiens (human) 29071 C1GALT1C1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2236 congenital afibrinogenemia HGNC:3694 Homo sapiens (human) 2266 FGG inference by association of genotype from phenotype used in manual assertion
  • PMID:11001903
  • PMID:15284111
  • RGD:7240710
DOID:0112006 immunodeficiency 69 HGNC:5438 Homo sapiens (human) 3458 IFNG inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0090074 hypogonadotropic hypogonadism 8 with or without anosmia HGNC:4510 Homo sapiens (human) 84634 KISS1R inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:162 cancer SGD:S000000935 Saccharomyces cerevisiae S288C 856870 GLC7 sequence similarity evidence used in manual assertion
  • PMID:26354769
DOID:8924 autoimmune thrombocytopenic purpura HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10435723
DOID:6713 cerebrovascular disease HGNC:10718 Homo sapiens (human) 6401 SELE inference by association of genotype from phenotype used in manual assertion
  • PMID:16843446
DOID:11198 DiGeorge syndrome MGI:98729 Mus musculus (house mouse) 21813 Tgfbr2 author statement supported by traceable reference
  • PMID:15741317
DOID:10283 prostate cancer HGNC:11848 Homo sapiens (human) 7097 TLR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:22311043
DOID:65 connective tissue disease WB:WBGene00022816 Caenorhabditis elegans 176076 fbn-1 combinatorial experimental and author inference evidence used in manual assertion
  • PMID:25798732
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Last updated: December 8, 2025