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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 10026 - 10050 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:2741 bilirubin metabolic disorder HGNC:4893 Homo sapiens (human) 3082 HGF direct assay evidence used in manual assertion
  • PMID:9073133
DOID:14499 Fabry disease HGNC:2707 Homo sapiens (human) 1636 ACE direct assay evidence used in manual assertion
  • PMID:20941593
DOID:718 autoimmune hemolytic anemia HGNC:2505 Homo sapiens (human) 1493 CTLA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:12555221
DOID:10652 Alzheimer's disease HGNC:7154 Homo sapiens (human) 4311 MME direct assay evidence used in manual assertion
  • PMID:19606063
DOID:3068 glioblastoma HGNC:943 Homo sapiens (human) 575 ADGRB1 direct assay evidence used in manual assertion
  • PMID:16244591
DOID:3393 coronary artery disease HGNC:7876 Homo sapiens (human) 4846 NOS3 inference by association of genotype from phenotype used in manual assertion
  • PMID:16284093
  • PMID:19761682
  • PMID:8564837
DOID:302 substance abuse HGNC:281 Homo sapiens (human) 150 ADRA2A inference by association of genotype from phenotype used in manual assertion
  • PMID:21140256
DOID:10873 Kuhnt-Junius degeneration HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:9512153
DOID:3393 coronary artery disease HGNC:3176 Homo sapiens (human) 1906 EDN1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18923236
DOID:0060249 scoliosis HGNC:3604 Homo sapiens (human) 2201 FBN2 inference by association of genotype from phenotype used in manual assertion
  • PMID:24833718
DOID:0110346 osteogenesis imperfecta type 10 HGNC:1546 Homo sapiens (human) 871 SERPINH1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:11764 Homo sapiens (human) 7038 TG direct assay evidence used in manual assertion
  • PMID:30016121
DOID:0110084 arrhythmogenic right ventricular dysplasia 13 HGNC:2511 Homo sapiens (human) 29119 CTNNA3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3209 junctional epidermolysis bullosa HGNC:2194 Homo sapiens (human) 1308 COL17A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:7550320
  • RGD:7240710
DOID:0080219 dystransthyretinemic hyperthyroxinemia HGNC:12405 Homo sapiens (human) 7276 TTR inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080199 colorectal carcinoma HGNC:7669 Homo sapiens (human) 10499 NCOA2 mutant phenotype evidence used in manual assertion
  • PMID:25823027
DOID:898 autosomal dominant polycystic kidney disease HGNC:9008 Homo sapiens (human) 5310 PKD1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21115670
  • PMID:8554072
DOID:11981 morbid obesity HGNC:320 Homo sapiens (human) 177 AGER direct assay evidence used in manual assertion
  • PMID:22828946
DOID:10608 celiac disease HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12404952
DOID:0110864 congenital stationary night blindness 1F HGNC:24783 Homo sapiens (human) 345193 LRIT3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:6364 migraine HGNC:19439 Homo sapiens (human) 338567 KCNK18 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:13382 megaloblastic anemia HGNC:14604 Homo sapiens (human) 81693 AMN inference by association of genotype from phenotype used in manual assertion
  • PMID:12590260
DOID:9669 senile cataract HGNC:8125 Homo sapiens (human) 4968 OGG1 inference by association of genotype from phenotype used in manual assertion
  • PMID:24868140
DOID:9119 acute myeloid leukemia HGNC:8064 Homo sapiens (human) 8021 NUP214 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080170 normophosphatemic familial tumoral calcinosis HGNC:1348 Homo sapiens (human) 54809 SAMD9 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.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: April 7, 2025