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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 9876 - 9900 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:0060589 Yunis-Varon syndrome HGNC:16873 Homo sapiens (human) 9896 FIG4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:321 HTLV-1-associated myelopathy/tropical spastic paraparesis HGNC:7794 Homo sapiens (human) 4790 NFKB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:22170554
DOID:6419 tetralogy of Fallot HGNC:7432 Homo sapiens (human) 4522 MTHFD1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18767138
DOID:6432 pulmonary hypertension HGNC:7873 Homo sapiens (human) 4843 NOS2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16813666
DOID:3526 cerebral infarction HGNC:9204 Homo sapiens (human) 5444 PON1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10729395
DOID:13359 Ehlers-Danlos syndrome HGNC:2210 Homo sapiens (human) 1290 COL5A2 inference by association of genotype from phenotype used in manual assertion
  • PMID:9425231
DOID:9975 cocaine dependence HGNC:8153 Homo sapiens (human) 4985 OPRD1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17622222
  • PMID:22795689
  • PMID:24533225
  • PMID:27449273
  • PMID:33953123
DOID:3312 bipolar disorder HGNC:4585 Homo sapiens (human) 2903 GRIN2A inference by association of genotype from phenotype used in manual assertion
  • PMID:12809987
DOID:0050741 alcohol dependence HGNC:4093 Homo sapiens (human) 2572 GAD2 inference by association of genotype from phenotype used in manual assertion
  • PMID:17034009
DOID:0050458 juvenile myelomonocytic leukemia HGNC:9644 Homo sapiens (human) 5781 PTPN11 inference by association of genotype from phenotype used in manual assertion
  • PMID:12717436
  • RGD:7240710
DOID:0111715 Schaaf-Yang syndrome HGNC:6814 Homo sapiens (human) 54551 MAGEL2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8947 diabetic retinopathy HGNC:4883 Homo sapiens (human) 3075 CFH inference by association of genotype from phenotype used in manual assertion
  • PMID:23296223
  • PMID:23864767
DOID:0111238 congenital muscular dystrophy-dystroglycanopathy type A13 HGNC:15685 Homo sapiens (human) 11041 B4GAT1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2957 pulmonary tuberculosis HGNC:7873 Homo sapiens (human) 4843 NOS2 inference by association of genotype from phenotype used in manual assertion
  • PMID:19575238
DOID:612 primary immunodeficiency disease HGNC:10937 Homo sapiens (human) 6573 SLC19A1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:7148 rheumatoid arthritis HGNC:4942 Homo sapiens (human) 3117 HLA-DQA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11454644
  • PMID:11482129
DOID:0111647 Schopf-Schulz-Passarge syndrome HGNC:13829 Homo sapiens (human) 80326 WNT10A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1171 hyperlipoproteinemia type V HGNC:17288 Homo sapiens (human) 116519 APOA5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1561 cognitive disorder HGNC:2928 Homo sapiens (human) 1756 DMD inference by association of genotype from phenotype used in manual assertion
  • PMID:24265581
DOID:0050741 alcohol dependence HGNC:8154 Homo sapiens (human) 4986 OPRK1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16924269
  • PMID:17622222
DOID:3883 Lynch syndrome HGNC:7325 Homo sapiens (human) 4436 MSH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:10404063
  • PMID:16500024
  • PMID:28218421
DOID:0060290 Ohdo syndrome, SBBYS variant HGNC:17582 Homo sapiens (human) 23522 KAT6B inference by association of genotype from phenotype used in manual assertion
  • PMID:22077973
  • RGD:7240710
DOID:0060601 alpha-2-plasmin inhibitor deficiency HGNC:9075 Homo sapiens (human) 5345 SERPINF2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110975 brachydactyly type B2 HGNC:7866 Homo sapiens (human) 9241 NOG inference by association of genotype from phenotype used in manual assertion
  • PMID:17668388
  • RGD:7240710
DOID:2841 asthma HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:12938145
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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: April 7, 2025