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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 6026 - 6050 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species ▲ Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:3910 lung adenocarcinoma HGNC:18505 Homo sapiens (human) 54894 RNF43 mutant phenotype evidence used in manual assertion
  • PMID:31286874
DOID:0112064 immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis HGNC:9802 Homo sapiens (human) 5880 RAC2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1270 hereditary hemorrhagic telangiectasia HGNC:175 Homo sapiens (human) 94 ACVRL1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15024723
  • PMID:16752392
  • PMID:17219009
  • PMID:18543223
  • RGD:7240710
DOID:8552 chronic myeloid leukemia HGNC:76 Homo sapiens (human) 25 ABL1 mutant phenotype evidence used in manual assertion
  • PMID:21481795
DOID:0112202 developmental and epileptic encephalopathy HGNC:18423 Homo sapiens (human) 9681 DEPDC5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12347 osteogenesis imperfecta HGNC:26185 Homo sapiens (human) 79879 CCDC134 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050983 spinocerebellar ataxia type 36 HGNC:15911 Homo sapiens (human) 10528 NOP56 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:1663 Homo sapiens (human) 948 CD36 direct assay evidence used in manual assertion
  • PMID:20134099
DOID:2957 pulmonary tuberculosis HGNC:3443 Homo sapiens (human) 2069 EREG inference by association of genotype from phenotype used in manual assertion
  • PMID:30634928
DOID:10159 osteonecrosis HGNC:537 Homo sapiens (human) 302 ANXA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:15784727
DOID:0110334 osteogenesis imperfecta type 1 HGNC:2197 Homo sapiens (human) 1277 COL1A1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1094 attention deficit hyperactivity disorder HGNC:3026 Homo sapiens (human) 1816 DRD5 inference by association of genotype from phenotype used in manual assertion
  • PMID:11032390
  • PMID:14699430
  • RGD:7240710
DOID:12241 beta thalassemia HGNC:2197 Homo sapiens (human) 1277 COL1A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12803121
DOID:6432 pulmonary hypertension HGNC:2634 Homo sapiens (human) 1573 CYP2J2 direct assay evidence used in manual assertion
  • PMID:20118222
DOID:10652 Alzheimer's disease HGNC:9052 Homo sapiens (human) 5328 PLAU inference by association of genotype from phenotype used in manual assertion
  • PMID:18076107
DOID:1210 optic neuritis HGNC:1516 Homo sapiens (human) 847 CAT direct assay evidence used in manual assertion
  • PMID:18055782
DOID:0111740 X-linked deafness 6 HGNC:2208 Homo sapiens (human) 1288 COL4A6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080736 Ehlers-Danlos syndrome musculocontractural type 1 HGNC:24464 Homo sapiens (human) 113189 CHST14 inference by association of genotype from phenotype used in manual assertion
  • PMID:20004762
  • PMID:26373698
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:2631 Homo sapiens (human) 1571 CYP2E1 inference by association of genotype from phenotype used in manual assertion
  • PMID:20364586
  • PMID:29765251
DOID:0050685 small cell carcinoma HGNC:9884 Homo sapiens (human) 5925 RB1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:552 pneumonia HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B inference by association of genotype from phenotype used in manual assertion
  • PMID:20811626
DOID:2217 Bernard-Soulier syndrome HGNC:4444 Homo sapiens (human) 2815 GP9 inference by association of genotype from phenotype used in manual assertion
  • PMID:28131619
  • PMID:8972003
  • RGD:7240710
DOID:9538 multiple myeloma HGNC:2505 Homo sapiens (human) 1493 CTLA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:11167807
DOID:0090011 immunodeficiency-centromeric instability-facial anomalies syndrome 4 HGNC:4861 Homo sapiens (human) 3070 HELLS inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112068 nuclear type mitochondrial complex I deficiency 5 HGNC:7707 Homo sapiens (human) 4719 NDUFS1 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