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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 13776 - 13800 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:0050771 pheochromocytoma HGNC:4800 Homo sapiens (human) 3028 HSD17B10 mutant phenotype evidence used in manual assertion
  • PMID:25879199
DOID:0080846 latent autoimmune diabetes in adults HGNC:2505 Homo sapiens (human) 1493 CTLA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:12021137
DOID:10763 hypertension RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf inference by association of genotype from phenotype used in manual assertion
  • PMID:9590569
DOID:9074 systemic lupus erythematosus HGNC:11158 Homo sapiens (human) 6632 SNRPD1 direct assay evidence used in manual assertion
  • PMID:12571858
DOID:12858 Huntington's disease HGNC:4586 Homo sapiens (human) 2904 GRIN2B inference by association of genotype from phenotype used in manual assertion
  • PMID:15742215
  • PMID:17569088
DOID:12716 newborn respiratory distress syndrome HGNC:1516 Homo sapiens (human) 847 CAT inference by association of genotype from phenotype used in manual assertion
  • PMID:22574884
DOID:5419 schizophrenia MGI:2148258 Mus musculus (house mouse) 111174 Taar1 author statement supported by traceable reference
  • PMID:17212650
DOID:12930 dilated cardiomyopathy HGNC:3049 Homo sapiens (human) 1829 DSG2 inference by association of genotype from phenotype used in manual assertion
  • PMID:18678517
DOID:783 end stage renal disease HGNC:11078 Homo sapiens (human) 6553 SLC9A5 inference by association of genotype from phenotype used in manual assertion
  • PMID:10642288
DOID:12859 choreatic disease HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17559688
DOID:0112072 nuclear type mitochondrial complex I deficiency 20 HGNC:21497 Homo sapiens (human) 28976 ACAD9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9256 colorectal cancer HGNC:9682 Homo sapiens (human) 11122 PTPRT inference by association of genotype from phenotype used in manual assertion
  • PMID:30200630
DOID:11266 Hantavirus hemorrhagic fever with renal syndrome HGNC:4953 Homo sapiens (human) 3127 HLA-DRB5 inference by association of genotype from phenotype used in manual assertion
  • PMID:25169964
DOID:2841 asthma HGNC:9591 Homo sapiens (human) 5729 PTGDR inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:687 hepatoblastoma HGNC:3002 Homo sapiens (human) 1800 DPEP1 mutant phenotype evidence used in manual assertion
  • PMID:31541079
DOID:10763 hypertension HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:11840488
DOID:1094 attention deficit hyperactivity disorder HGNC:644 Homo sapiens (human) 367 AR inference by association of genotype from phenotype used in manual assertion
  • PMID:10380986
DOID:0110698 hypotrichosis 1 HGNC:11161 Homo sapiens (human) 6635 SNRPE inference by association of genotype from phenotype used in manual assertion
  • PMID:23246290
DOID:12798 mucopolysaccharidosis HGNC:5320 Homo sapiens (human) 3373 HYAL1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10339581
DOID:0050214 Lambert-Eaton myasthenic syndrome HGNC:1389 Homo sapiens (human) 774 CACNA1B direct assay evidence used in manual assertion
  • PMID:16289869
DOID:178 vascular disease HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:22081301
DOID:674 cleft palate MGI:1921642 Mus musculus (house mouse) 74392 Specc1l author statement supported by traceable reference
  • PMID:34302166
DOID:2841 asthma HGNC:5331 Homo sapiens (human) 64127 NOD2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16008671
DOID:2921 glomerulonephritis HGNC:3535 Homo sapiens (human) 2147 F2 direct assay evidence used in manual assertion
  • PMID:17519558
DOID:0111503 Li-Fraumeni syndrome 1 HGNC:11998 Homo sapiens (human) 7157 TP53 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