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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 11851 - 11875 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:0110299 autosomal recessive limb-girdle muscular dystrophy type 2I MGI:2447586 Mus musculus (house mouse) 243853 Fkrp
  • MGI:6194238
  • PMID:20675713
  • PMID:24234655
  • PMID:26574668
DOID:0050560 Walker-Warburg syndrome FB:FBgn0086368 Drosophila melanogaster (fruit fly) 31024 tw CG12311
  • MGI:6194238
  • PMID:20644630
DOID:1919 Lesch-Nyhan syndrome HGNC:5157 Homo sapiens (human) 3251 HPRT1
  • MGI:6194238
  • PMID:20638392
  • PMID:24940672
  • RGD:7240710
DOID:10763 hypertension HGNC:12663 Homo sapiens (human) 7412 VCAM1
  • MGI:6194238
  • PMID:20569722
DOID:9352 type 2 diabetes mellitus RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
  • PMID:20559450
DOID:9870 galactosemia FB:FBgn0263200 Drosophila melanogaster (fruit fly) 33935 Galt
  • MGI:6194238
  • PMID:20519569
  • PMID:22736462
  • PMID:22773758
  • PMID:23758052
  • PMID:25326312
DOID:9870 galactosemia FB:FBgn0035147 Drosophila melanogaster (fruit fly) 38076 Gale
  • MGI:6194238
  • PMID:20519568
  • PMID:22654673
  • PMID:27466186
DOID:1073 renal hypertension HGNC:2634 Homo sapiens (human) 1573 CYP2J2
  • MGI:6194238
  • PMID:20495177
DOID:0080208 metabolic dysfunction-associated steatotic liver disease RGD:3000 Rattus norvegicus (Norway rat) 25608 Lep
  • MGI:6194238
  • PMID:20476641
  • PMID:30052309
DOID:5844 myocardial infarction HGNC:391 Homo sapiens (human) 207 AKT1
  • MGI:6194238
  • PMID:20467748
DOID:10763 hypertension RGD:3932 Rattus norvegicus (Norway rat) 54315 Ucp2
  • MGI:6194238
  • PMID:20404217
DOID:12365 malaria HGNC:9020 Homo sapiens (human) 5313 PKLR
  • MGI:6194238
  • PMID:20377593
DOID:5844 myocardial infarction RGD:2081 Rattus norvegicus (Norway rat) 24185 Akt1
  • MGI:6194238
  • PMID:20352476
DOID:9269 maple syrup urine disease HGNC:987 Homo sapiens (human) 594 BCKDHB
  • MGI:6194238
  • PMID:2022752
DOID:2048 autoimmune hepatitis HGNC:4606 Homo sapiens (human) 2923 PDIA3
  • MGI:6194238
  • PMID:20208391
DOID:2841 asthma HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
  • PMID:20205697
DOID:0050833 orotic aciduria WB:WBGene00011559 Caenorhabditis elegans 176453 umps-1
  • MGI:6194238
  • PMID:20148972
  • PMID:24262006
DOID:224 transient cerebral ischemia RGD:2721 Rattus norvegicus (Norway rat) 24401 Got1
  • MGI:6194238
  • PMID:20145654
DOID:10763 hypertension HGNC:1929 Homo sapiens (human) 1113 CHGA
  • MGI:6194238
  • PMID:20113265
  • PMID:21061160
DOID:206 hereditary multiple exostoses MGI:894663 Mus musculus (house mouse) 14042 Ext1
  • MGI:6194238
  • PMID:20080592
  • PMID:20534475
  • PMID:28445472
DOID:10763 hypertension HGNC:3402 Homo sapiens (human) 2053 EPHX2
  • MGI:6194238
  • PMID:20065888
DOID:10763 hypertension RGD:3000 Rattus norvegicus (Norway rat) 25608 Lep
  • MGI:6194238
  • PMID:20059648
DOID:5082 liver cirrhosis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • MGI:6194238
  • PMID:20006396
DOID:9970 obesity HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • MGI:6194238
  • PMID:20004360
DOID:2861 congenital nonspherocytic hemolytic anemia HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
  • PMID:1999409
  • PMID:24923766

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