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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 13751 - 13775 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:0060989 short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1 HGNC:1069 Homo sapiens (human) 650 BMP2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:5419 schizophrenia HGNC:5233 Homo sapiens (human) 3304 HSPA1B inference by association of genotype from phenotype used in manual assertion
  • PMID:18299791
DOID:0050700 cardiomyopathy HGNC:6357 Homo sapiens (human) 3816 KLK1 direct assay evidence used in manual assertion
  • PMID:15117887
DOID:3908 lung non-small cell carcinoma HGNC:7794 Homo sapiens (human) 4790 NFKB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:26221384
DOID:5176 renal Wilms' tumor HGNC:1066 Homo sapiens (human) 648 BMI1 mutant phenotype evidence used in manual assertion
  • PMID:18467665
DOID:0050741 alcohol dependence HGNC:281 Homo sapiens (human) 150 ADRA2A inference by association of genotype from phenotype used in manual assertion
  • PMID:21070505
DOID:0111865 MEND syndrome HGNC:3133 Homo sapiens (human) 10682 EBP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:13223 uterine fibroid HGNC:2213 Homo sapiens (human) 1293 COL6A3 inference by association of genotype from phenotype used in manual assertion
  • PMID:23818951
DOID:4607 biliary tract cancer HGNC:2595 Homo sapiens (human) 1543 CYP1A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:19168589
DOID:0110165 Charcot-Marie-Tooth disease type 2E HGNC:7739 Homo sapiens (human) 4747 NEFL inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3908 lung non-small cell carcinoma HGNC:1100 Homo sapiens (human) 672 BRCA1 direct assay evidence used in manual assertion
  • PMID:23128816
  • PMID:23335114
DOID:9074 systemic lupus erythematosus HGNC:10305 Homo sapiens (human) 9045 RPL14 direct assay evidence used in manual assertion
  • PMID:12051391
DOID:2560 morphine dependence HGNC:2228 Homo sapiens (human) 1312 COMT inference by association of genotype from phenotype used in manual assertion
  • PMID:30211780
DOID:0060680 pigment dispersion syndrome MGI:88451 Mus musculus (house mouse) 12822 Col18a1 author statement supported by traceable reference
  • PMID:12766032
DOID:0111063 hyperphosphatemic familial tumoral calcinosis MGI:894695 Mus musculus (house mouse) 14425 Galnt3 author statement supported by traceable reference
  • PMID:19213845
  • PMID:22912827
DOID:0081333 Wiedemann-Rautenstrauch syndrome HGNC:30074 Homo sapiens (human) 11128 POLR3A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:13375 temporal arteritis HGNC:11850 Homo sapiens (human) 7099 TLR4 inference by association of genotype from phenotype used in manual assertion
  • PMID:19531762
DOID:10652 Alzheimer's disease HGNC:6619 Homo sapiens (human) 3990 LIPC inference by association of genotype from phenotype used in manual assertion
  • PMID:17175070
DOID:0060496 respiratory allergy HGNC:11850 Homo sapiens (human) 7099 TLR4 inference by association of genotype from phenotype used in manual assertion
  • PMID:21704886
DOID:0014667 disease of metabolism HGNC:11289 Homo sapiens (human) 6720 SREBF1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18692268
DOID:11450 allergic cutaneous vasculitis HGNC:2438 Homo sapiens (human) 1440 CSF3 direct assay evidence used in manual assertion
  • PMID:20100783
DOID:12583 velocardiofacial syndrome MGI:1313268 Mus musculus (house mouse) 12667 Chrd author statement supported by traceable reference
  • PMID:12810603
DOID:0110959 Gaucher's disease type III HGNC:4177 Homo sapiens (human) 2629 GBA1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080162 lupus nephritis HGNC:320 Homo sapiens (human) 177 AGER inference by association of genotype from phenotype used in manual assertion
  • PMID:22513366
DOID:10587 Krabbe disease MGI:97783 Mus musculus (house mouse) 19156 Psap author statement supported by traceable reference
  • PMID:11371512
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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

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Last updated: December 8, 2025