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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 11726 - 11750 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▼
DOID:0050558 Ullrich congenital muscular dystrophy MGI:88459 Mus musculus (house mouse) 12833 Col6a1
  • MGI:6194238
  • PMID:28043812
DOID:0080433 developmental and epileptic encephalopathy 51 SGD:S000001568 Saccharomyces cerevisiae S288C 853777 MDH1
  • MGI:6194238
  • PMID:27989324
DOID:1742 drug psychosis HGNC:4092 Homo sapiens (human) 2571 GAD1
  • MGI:6194238
  • PMID:27967329
DOID:0111459 classic galactosemia FB:FBgn0263200 Drosophila melanogaster (fruit fly) 33935 Galt
  • MGI:6194238
  • PMID:27562100
DOID:3347 osteosarcoma RGD:3889 Rattus norvegicus (Norway rat) 24842 Tp53
  • MGI:6194238
  • PMID:27528400
DOID:14500 fucosidosis MGI:95593 Mus musculus (house mouse) 71665 Fuca1
  • MGI:6194238
  • PMID:27491075
DOID:10763 hypertension RGD:3001 Rattus norvegicus (Norway rat) 24536 Lepr
  • MGI:6194238
  • PMID:27465994
  • PMID:32710530
DOID:3070 high grade glioma SGD:S000002224 Saccharomyces cerevisiae S288C 851493 IDP1
  • MGI:6194238
  • PMID:27427385
DOID:3070 high grade glioma SGD:S000004164 Saccharomyces cerevisiae S288C 850871 IDP2
  • MGI:6194238
  • PMID:27427385
DOID:0050560 Walker-Warburg syndrome SGD:S000003904 Saccharomyces cerevisiae S288C 853608 PMT4
  • MGI:6194238
  • PMID:27358400
DOID:0110125 Bardet-Biedl syndrome 3 MGI:1927136 Mus musculus (house mouse) 56297 Arl6
  • MGI:6194238
  • PMID:27170093
DOID:0060740 methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency HGNC:7526 Homo sapiens (human) 4594 MMUT
  • MGI:6194238
  • PMID:27167370
  • RGD:7240710
DOID:0111454 SHORT syndrome MGI:97583 Mus musculus (house mouse) 18708 Pik3r1
  • MGI:6194238
  • PMID:26974159
DOID:0050570 congenital disorder of glycosylation type I FB:FBgn0036300 Drosophila melanogaster (fruit fly) 39436 Pmm2
  • MGI:6194238
  • PMID:26940433
DOID:0080563 congenital disorder of glycosylation Ik SGD:S000000314 Saccharomyces cerevisiae S288C 852407 ALG1
  • MGI:6194238
  • PMID:26931382
DOID:5082 liver cirrhosis RGD:3870 Rattus norvegicus (Norway rat) 29260 Tlr4
  • MGI:6194238
  • PMID:26809353
  • PMID:27061671
  • PMID:32626927
DOID:1612 breast cancer HGNC:11998 Homo sapiens (human) 7157 TP53
  • MGI:6194238
  • PMID:26666818
  • RGD:7240710
DOID:0060202 amyotrophic lateral sclerosis type 11 FB:FBgn0031611 Drosophila melanogaster (fruit fly) 33658 FIG4
  • MGI:6194238
  • PMID:26662798
DOID:0110474 autosomal recessive nonsyndromic deafness 18B MGI:1202064 Mus musculus (house mouse) 18419 Otog
  • MGI:6194238
  • PMID:26636018
DOID:8283 peritonitis HGNC:11892 Homo sapiens (human) 7124 TNF
  • MGI:6194238
  • PMID:26601826
DOID:14500 fucosidosis HGNC:4006 Homo sapiens (human) 2517 FUCA1
  • MGI:6194238
  • PMID:2642067
  • RGD:7240710
DOID:2871 endometrial carcinoma RGD:3889 Rattus norvegicus (Norway rat) 24842 Tp53
  • MGI:6194238
  • PMID:26353976
DOID:83 cataract HGNC:6708 Homo sapiens (human) 4047 LSS
  • MGI:6194238
  • PMID:26200341
DOID:684 hepatocellular carcinoma RGD:620916 Rattus norvegicus (Norway rat) 170911 Pik3ca
  • MGI:6194238
  • PMID:25999787
DOID:898 autosomal dominant polycystic kidney disease HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
  • PMID:25920554

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Last updated: August 19, 2024