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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 July 29, 2024
Displaying entries 12076 - 12100 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:5844 myocardial infarction HGNC:6623 Homo sapiens (human) 9388 LIPG
  • PMID:17526978
DOID:0090075 hypogonadotropic hypogonadism 15 with or without anosmia HGNC:5201 Homo sapiens (human) 9394 HS6ST1
  • RGD:7240710
DOID:1793 pancreatic cancer MGI:2136878 Mus musculus (house mouse) 93961 B3galt5
  • MGI:6194238
DOID:0070382 developmental and epileptic encephalopathy 95 HGNC:14937 Homo sapiens (human) 94005 PIGS
  • RGD:7240710
DOID:2841 asthma HGNC:16036 Homo sapiens (human) 94101 ORMDL1
  • MGI:6194238
DOID:12930 dilated cardiomyopathy HGNC:3575 Homo sapiens (human) 9415 FADS2
  • PMID:24284026
DOID:9744 type 1 diabetes mellitus HGNC:3575 Homo sapiens (human) 9415 FADS2
  • MGI:6194238
DOID:6000 congestive heart failure HGNC:3575 Homo sapiens (human) 9415 FADS2
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:3575 Homo sapiens (human) 9415 FADS2
  • MGI:6194238
DOID:3146 lipid metabolism disorder HGNC:3575 Homo sapiens (human) 9415 FADS2
  • MGI:6194238
DOID:5804 discrete subaortic stenosis HGNC:3575 Homo sapiens (human) 9415 FADS2
  • MGI:6194238
DOID:0080576 spondyloepimetaphyseal dysplasia, Genevieve-type MGI:2149820 Mus musculus (house mouse) 94181 Nans
  • MGI:6194238
DOID:0060050 autoimmune disease of blood MGI:2151071 Mus musculus (house mouse) 94192 C1galt1
  • MGI:6194238
DOID:0111070 congenital bile acid synthesis defect 3 HGNC:2652 Homo sapiens (human) 9420 CYP7B1
  • RGD:7240710
DOID:0110810 hereditary spastic paraplegia 5A HGNC:2652 Homo sapiens (human) 9420 CYP7B1
  • RGD:7240710
DOID:9743 diabetic neuropathy RGD:619850 Rattus norvegicus (Norway rat) 94203 Pgf
  • MGI:6194238
DOID:8947 diabetic retinopathy RGD:619850 Rattus norvegicus (Norway rat) 94203 Pgf
  • PMID:21408222
DOID:783 end stage renal disease RGD:619850 Rattus norvegicus (Norway rat) 94203 Pgf
  • PMID:16543713
DOID:4977 lymphedema RGD:619850 Rattus norvegicus (Norway rat) 94203 Pgf
  • MGI:6194238
DOID:10763 hypertension RGD:619850 Rattus norvegicus (Norway rat) 94203 Pgf
  • MGI:6194238
DOID:7148 rheumatoid arthritis RGD:619850 Rattus norvegicus (Norway rat) 94203 Pgf
  • MGI:6194238
DOID:6432 pulmonary hypertension RGD:619850 Rattus norvegicus (Norway rat) 94203 Pgf
  • MGI:6194238
DOID:4450 renal cell carcinoma RGD:619850 Rattus norvegicus (Norway rat) 94203 Pgf
  • MGI:6194238
DOID:3407 carotid artery disease RGD:619850 Rattus norvegicus (Norway rat) 94203 Pgf
  • MGI:6194238
DOID:10923 sickle cell anemia RGD:619850 Rattus norvegicus (Norway rat) 94203 Pgf
  • MGI:6194238

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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: August 19, 2024