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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 10001 - 10025 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:0050545 visceral heterotaxy HGNC:18053 Homo sapiens (human) 168507 PKD1L1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1612 breast cancer HGNC:3570 Homo sapiens (human) 2181 ACSL3 inference by association of genotype from phenotype used in manual assertion
  • PMID:28977883
DOID:0070482 spinal neurofibromatosis HGNC:7765 Homo sapiens (human) 4763 NF1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110402 retinitis pigmentosa 45 HGNC:2151 Homo sapiens (human) 1258 CNGB1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050742 nicotine dependence HGNC:7978 Homo sapiens (human) 2908 NR3C1 inference by association of genotype from phenotype used in manual assertion
  • PMID:23543128
DOID:9744 type 1 diabetes mellitus HGNC:11588 Homo sapiens (human) 6908 TBP inference by association of genotype from phenotype used in manual assertion
  • PMID:15381080
DOID:13533 osteopetrosis HGNC:11028 Homo sapiens (human) 6522 SLC4A2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12930 dilated cardiomyopathy HGNC:3052 Homo sapiens (human) 1832 DSP inference by association of genotype from phenotype used in manual assertion
  • PMID:11063735
DOID:7148 rheumatoid arthritis HGNC:11916 Homo sapiens (human) 7132 TNFRSF1A inference by association of genotype from phenotype used in manual assertion
  • PMID:25311255
DOID:9352 type 2 diabetes mellitus HGNC:11289 Homo sapiens (human) 6720 SREBF1 inference by association of genotype from phenotype used in manual assertion
  • PMID:18692268
DOID:0060708 lymphoproliferative syndrome 2 HGNC:11922 Homo sapiens (human) 939 CD27 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080549 Noonan syndrome with multiple lentigines 2 HGNC:9829 Homo sapiens (human) 5894 RAF1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080176 meningococcal meningitis HGNC:11850 Homo sapiens (human) 7099 TLR4 inference by association of genotype from phenotype used in manual assertion
  • PMID:23691182
DOID:0110913 adult hypophosphatasia HGNC:438 Homo sapiens (human) 249 ALPL inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2216 factor V deficiency HGNC:6631 Homo sapiens (human) 3998 LMAN1 inference by association of genotype from phenotype used in manual assertion
  • PMID:9546392
DOID:2986 IgA glomerulonephritis HGNC:243 Homo sapiens (human) 118 ADD1 inference by association of genotype from phenotype used in manual assertion
  • PMID:19838659
DOID:1882 atrial heart septal defect HGNC:11187 Homo sapiens (human) 6654 SOS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17143285
DOID:1749 squamous cell carcinoma HGNC:13861 Homo sapiens (human) 11178 LZTS1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10097140
DOID:9352 type 2 diabetes mellitus HGNC:13633 Homo sapiens (human) 9370 ADIPOQ inference by association of genotype from phenotype used in manual assertion
  • PMID:24655058
DOID:0111057 platelet-type bleeding disorder 11 HGNC:14388 Homo sapiens (human) 51206 GP6 inference by association of genotype from phenotype used in manual assertion
  • PMID:23815599
  • RGD:7240710
DOID:0050741 alcohol dependence HGNC:5293 Homo sapiens (human) 3356 HTR2A inference by association of genotype from phenotype used in manual assertion
  • PMID:19060480
  • PMID:21930285
  • PMID:23321485
DOID:0060848 developmental and epileptic encephalopathy 9 HGNC:14270 Homo sapiens (human) 57526 PCDH19 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110079 Leber congenital amaurosis 8 HGNC:2343 Homo sapiens (human) 23418 CRB1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050741 alcohol dependence HGNC:5287 Homo sapiens (human) 3351 HTR1B inference by association of genotype from phenotype used in manual assertion
  • PMID:11104852
  • PMID:12022963
  • PMID:21172311
  • PMID:21906503
  • PMID:22005095
DOID:10595 Charcot-Marie-Tooth disease HGNC:30348 Homo sapiens (human) 55703 POLR3B 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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