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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 October 9, 2024
Displaying entries 71626 - 71650 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:2018 hyperinsulinism HGNC:6619 Homo sapiens (human) 3990 LIPC
  • MGI:6194238
  • PMID:11095452
  • PMID:1592086
DOID:0050633 ocular albinism 1 MGI:107193 Mus musculus (house mouse) 18241 Gpr143
  • MGI:6194238
  • PMID:11092754
DOID:1574 alcohol use disorder FB:FBgn0010329 Drosophila melanogaster (fruit fly) 31718 Tbh
  • MGI:6194238
  • PMID:11086999
  • PMID:16094367
DOID:0110152 Charcot-Marie-Tooth disease type 1B MGI:103177 Mus musculus (house mouse) 17528 Mpz
  • MGI:6194238
  • PMID:11086005
  • PMID:16495463
  • PMID:22689911
  • PMID:7581451
DOID:9352 type 2 diabetes mellitus MGI:109334 Mus musculus (house mouse) 384783 Irs2
  • MGI:6194238
  • PMID:11078455
  • PMID:15467829
  • PMID:9495343
DOID:10763 hypertension HGNC:3176 Homo sapiens (human) 1906 EDN1
  • MGI:6194238
  • PMID:11078355
  • PMID:17444275
  • PMID:18496905
DOID:11247 disseminated intravascular coagulation HGNC:11760 Homo sapiens (human) 7035 TFPI
  • MGI:6194238
  • PMID:11074537
  • PMID:8292719
  • PMID:8914465
  • PMID:8929465
DOID:10283 prostate cancer HGNC:3689 Homo sapiens (human) 2263 FGFR2
  • MGI:6194238
  • PMID:11069376
  • PMID:11170144
  • PMID:12111699
  • PMID:9285567
DOID:9074 systemic lupus erythematosus MGI:88228 Mus musculus (house mouse) 12268 C4b
  • MGI:6194238
  • PMID:11067882
DOID:12716 newborn respiratory distress syndrome HGNC:10798 Homo sapiens (human) 653509 SFTPA1
  • MGI:6194238
  • PMID:11063734
DOID:12716 newborn respiratory distress syndrome HGNC:10801 Homo sapiens (human) 6439 SFTPB
  • MGI:6194238
  • PMID:11063734
  • PMID:12424586
  • PMID:12490037
  • PMID:18353230
  • PMID:7832777
DOID:0050545 visceral heterotaxy HGNC:33983 Homo sapiens (human) 653275 CFC1B
  • MGI:6194238
  • PMID:11062482
  • PMID:25423076
DOID:0050948 autosomal dominant hypophosphatemic rickets HGNC:3680 Homo sapiens (human) 8074 FGF23
  • MGI:6194238
  • PMID:11062477
  • PMID:19655082
  • RGD:7240710
DOID:14323 Marfan syndrome HGNC:3603 Homo sapiens (human) 2200 FBN1
  • MGI:6194238
  • PMID:11059536
  • PMID:11453977
  • PMID:11702223
  • PMID:15221638
  • PMID:16220557
  • PMID:16222657
  • PMID:16617303
  • PMID:16971892
  • PMID:17718856
  • PMID:17984934
  • PMID:18435798
  • PMID:19328768
  • PMID:20886638
  • PMID:21907952
  • PMID:21976953
  • PMID:22772377
  • PMID:22876116
  • PMID:23592911
  • PMID:25613431
  • PMID:25729264
  • PMID:26787436
  • PMID:8863159
  • PMID:8882780
  • PMID:8894692
  • PMID:9236141
  • RGD:7240710
DOID:0110313 hypertrophic cardiomyopathy 7 MGI:98783 Mus musculus (house mouse) 21954 Tnni3
  • MGI:6194238
  • PMID:11055985
  • PMID:18096573
DOID:14330 Parkinson's disease HGNC:11936 Homo sapiens (human) 356 FASLG
  • MGI:6194238
  • PMID:11054182
DOID:2921 glomerulonephritis HGNC:6156 Homo sapiens (human) 3690 ITGB3
  • MGI:6194238
  • PMID:11051455
DOID:9352 type 2 diabetes mellitus HGNC:6126 Homo sapiens (human) 8660 IRS2
  • MGI:6194238
  • PMID:11030756
  • RGD:7240710
DOID:2842 Jervell-Lange Nielsen syndrome MGI:96673 Mus musculus (house mouse) 16509 Kcne1
  • MGI:6194238
  • PMID:11003695
  • PMID:11223304
  • PMID:11438691
DOID:2236 congenital afibrinogenemia HGNC:3694 Homo sapiens (human) 2266 FGG
  • MGI:6194238
  • PMID:11001903
  • PMID:15284111
  • RGD:7240710
DOID:10763 hypertension HGNC:6554 Homo sapiens (human) 3953 LEPR
  • MGI:6194238
  • PMID:10999797
DOID:0110679 congenital myasthenic syndrome 4C MGI:87894 Mus musculus (house mouse) 11448 Chrne
  • MGI:6194238
  • PMID:10998094
DOID:10763 hypertension RGD:2071 Rattus norvegicus (Norway rat) 81638 Agtr1b
  • MGI:6194238
  • PMID:10994756
DOID:4450 renal cell carcinoma HGNC:8125 Homo sapiens (human) 4968 OGG1
  • MGI:6194238
  • PMID:10987279
  • RGD:7240710
DOID:9074 systemic lupus erythematosus MGI:95499 Mus musculus (house mouse) 14130 Fcgr2b
  • MGI:6194238
  • PMID:10981970

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 9, 2024