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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 70001 - 70025 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1287 cardiovascular system disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • PMID:18162502
DOID:10652 Alzheimer's disease HGNC:9237 Homo sapiens (human) 10891 PPARGC1A
  • MGI:6194238
  • PMID:19273754
DOID:0111238 congenital muscular dystrophy-dystroglycanopathy type A13 MGI:1919680 Mus musculus (house mouse) 108902 B4gat1
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 MGI:1919680 Mus musculus (house mouse) 108902 B4gat1
  • PMID:23217742
DOID:0050560 Walker-Warburg syndrome MGI:1919680 Mus musculus (house mouse) 108902 B4gat1
  • MGI:6194238
DOID:3969 thyroid gland papillary carcinoma HGNC:12755 Homo sapiens (human) 10885 WDR3
  • PMID:20578902
DOID:1574 alcohol use disorder MGI:1918614 Mus musculus (house mouse) 108829 Jmjd1c
  • MGI:6194238
DOID:2945 severe acute respiratory syndrome HGNC:1820 Homo sapiens (human) 1088 CEACAM8
  • PMID:19635508
DOID:3498 pancreatic ductal adenocarcinoma HGNC:16980 Homo sapiens (human) 10878 CFHR3
  • PMID:32663515
DOID:0080301 atypical hemolytic-uremic syndrome HGNC:16980 Homo sapiens (human) 10878 CFHR3
  • RGD:7240710
DOID:0110014 age related macular degeneration 1 HGNC:16980 Homo sapiens (human) 10878 CFHR3
  • RGD:7240710
DOID:0040094 autoimmune glomerulonephritis HGNC:3696 Homo sapiens (human) 10875 FGL2
  • MGI:6194238
DOID:9970 obesity HGNC:7859 Homo sapiens (human) 10874 NMU
  • MGI:6194238
  • PMID:16984985
DOID:10652 Alzheimer's disease Xenbase:XB-GENE-17339244 Xenopus laevis (African clawed frog) 108719811 plcd1.S
  • MGI:6194238
DOID:0080081 nonsyndromic congenital nail disorder 3 Xenbase:XB-GENE-17339244 Xenopus laevis (African clawed frog) 108719811 plcd1.S
  • MGI:6194238
DOID:9256 colorectal cancer Xenbase:XB-GENE-17330127 Xenopus laevis (African clawed frog) 108719043 galnt12.L
  • MGI:6194238
DOID:0080573 congenital disorder of glycosylation Ix Xenbase:XB-GENE-17341012 Xenopus laevis (African clawed frog) 108718938 stt3b.L
  • MGI:6194238
DOID:0080081 nonsyndromic congenital nail disorder 3 Xenbase:XB-GENE-6485790 Xenopus laevis (African clawed frog) 108718712 plcd1.L
  • MGI:6194238
DOID:10652 Alzheimer's disease Xenbase:XB-GENE-6485790 Xenopus laevis (African clawed frog) 108718712 plcd1.L
  • MGI:6194238
DOID:1574 alcohol use disorder Xenbase:XB-GENE-17330217 Xenopus laevis (African clawed frog) 108718183 st6gal1.S
  • MGI:6194238
DOID:1094 attention deficit hyperactivity disorder Xenbase:XB-GENE-6486769 Xenopus laevis (African clawed frog) 108717884 ust.S
  • MGI:6194238
DOID:0080693 Noonan syndrome-like disorder with loose anagen hair 2 Xenbase:XB-GENE-17344746 Xenopus laevis (African clawed frog) 108717671 ppp1cb.S
  • MGI:6194238
DOID:0090075 hypogonadotropic hypogonadism 15 with or without anosmia Xenbase:XB-GENE-17335472 Xenopus laevis (African clawed frog) 108717161 hs6st1.L
  • MGI:6194238
DOID:1574 alcohol use disorder Xenbase:XB-GENE-6486698 Xenopus laevis (African clawed frog) 108717116 st6gal1.L
  • MGI:6194238
DOID:5419 schizophrenia Xenbase:XB-GENE-17334879 Xenopus laevis (African clawed frog) 108716933 b3gat2.L
  • MGI:6194238

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024