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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:1612 breast cancer HGNC:2505 Homo sapiens (human) 1493 CTLA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:17825114
DOID:10584 retinitis pigmentosa HGNC:30859 Homo sapiens (human) 23020 SNRNP200 inference by association of genotype from phenotype used in manual assertion
  • PMID:19710410
  • PMID:19878916
DOID:13636 Fanconi anemia HGNC:1101 Homo sapiens (human) 675 BRCA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:12065746
DOID:0090129 carnitine palmitoyltransferase I deficiency HGNC:2328 Homo sapiens (human) 1374 CPT1A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:988 mitral valve prolapse HGNC:3603 Homo sapiens (human) 2200 FBN1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12918850
DOID:1561 cognitive disorder HGNC:1033 Homo sapiens (human) 627 BDNF inference by association of genotype from phenotype used in manual assertion
  • PMID:23517654
DOID:1474 aggressive periodontitis HGNC:10618 Homo sapiens (human) 6347 CCL2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21264360
DOID:3910 lung adenocarcinoma HGNC:3691 Homo sapiens (human) 2264 FGFR4 inference by association of genotype from phenotype used in manual assertion
  • PMID:16061909
  • PMID:19296538
DOID:0081267 graft-versus-host disease HGNC:5991 Homo sapiens (human) 3552 IL1A inference by association of genotype from phenotype used in manual assertion
  • PMID:23645090
DOID:0080071 mucolipidosis III alpha/beta HGNC:29670 Homo sapiens (human) 79158 GNPTAB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060793 hypomyelinating leukodystrophy 5 HGNC:24587 Homo sapiens (human) 84668 HYCC1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:6364 migraine HGNC:7876 Homo sapiens (human) 4846 NOS3 inference by association of genotype from phenotype used in manual assertion
  • PMID:16123422
DOID:4971 myelofibrosis HGNC:7132 Homo sapiens (human) 4297 KMT2A inference by association of genotype from phenotype used in manual assertion
  • PMID:35731275
DOID:9240 erythromelalgia HGNC:10597 Homo sapiens (human) 6335 SCN9A inference by association of genotype from phenotype used in manual assertion
  • PMID:14985375
  • PMID:16216943
  • RGD:7240710
DOID:0110682 congenital myasthenic syndrome 16 HGNC:10591 Homo sapiens (human) 6329 SCN4A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3910 lung adenocarcinoma HGNC:11730 Homo sapiens (human) 7015 TERT inference by association of genotype from phenotype used in manual assertion
  • PMID:19955392
  • PMID:23738012
  • PMID:23908149
  • PMID:24761905
  • PMID:31935503
DOID:399 tuberculosis HGNC:1641 Homo sapiens (human) 30835 CD209 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050848 obstructive sleep apnea HGNC:7997 Homo sapiens (human) 3084 NRG1 inference by association of genotype from phenotype used in manual assertion
  • PMID:25325441
DOID:1059 intellectual disability HGNC:1938 Homo sapiens (human) 1120 CHKB inference by association of genotype from phenotype used in manual assertion
  • PMID:21665002
DOID:2355 anemia HGNC:10908 Homo sapiens (human) 4891 SLC11A2 inference by association of genotype from phenotype used in manual assertion
  • PMID:17510944
DOID:8158 complement component 5 deficiency HGNC:1331 Homo sapiens (human) 727 C5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10652 Alzheimer's disease HGNC:4617 Homo sapiens (human) 2932 GSK3B inference by association of genotype from phenotype used in manual assertion
  • PMID:19154537
  • PMID:24101602
DOID:3393 coronary artery disease HGNC:13633 Homo sapiens (human) 9370 ADIPOQ inference by association of genotype from phenotype used in manual assertion
  • PMID:27218147
DOID:0070484 Legius syndrome HGNC:20249 Homo sapiens (human) 161742 SPRED1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2377 multiple sclerosis HGNC:8760 Homo sapiens (human) 5133 PDCD1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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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: April 7, 2025