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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 11901 - 11925 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:9256 colorectal cancer HGNC:19877 Homo sapiens (human) 79695 GALNT12
  • RGD:7240710
DOID:5723 optic atrophy HGNC:19691 Homo sapiens (human) 51102 MECR
  • RGD:7240710
DOID:9256 colorectal cancer HGNC:1097 Homo sapiens (human) 673 BRAF
  • RGD:7240710
DOID:0080596 hyper IgE recurrent infection syndrome 4 HGNC:6021 Homo sapiens (human) 3572 IL6ST
  • RGD:7240710
DOID:0111230 congenital muscular dystrophy-dystroglycanopathy type A11 HGNC:28596 Homo sapiens (human) 148789 B3GALNT2
  • RGD:7240710
DOID:0080502 GM1 gangliosidosis type 1 HGNC:4298 Homo sapiens (human) 2720 GLB1
  • RGD:7240710
DOID:0111389 mucopolysaccharidosis Ih/s HGNC:5391 Homo sapiens (human) 3425 IDUA
  • RGD:7240710
DOID:0110790 hereditary spastic paraplegia 39 HGNC:16268 Homo sapiens (human) 10908 PNPLA6
  • RGD:7240710
DOID:0080561 congenital disorder of glycosylation Ii HGNC:23159 Homo sapiens (human) 85365 ALG2
  • RGD:7240710
DOID:0050439 Usher syndrome HGNC:24102 Homo sapiens (human) 22901 ARSG
  • RGD:7240710
DOID:0080718 GNE myopathy HGNC:23657 Homo sapiens (human) 10020 GNE
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:4456 Homo sapiens (human) 2820 GPD2
  • RGD:7240710
DOID:0050564 autosomal dominant nonsyndromic deafness HGNC:8984 Homo sapiens (human) 5298 PI4KB
  • RGD:7240710
DOID:2582 acatalasia HGNC:1516 Homo sapiens (human) 847 CAT
  • RGD:7240710
DOID:0080557 congenital disorder of glycosylation Ie HGNC:3005 Homo sapiens (human) 8813 DPM1
  • RGD:7240710
DOID:0111420 familial GPIHBP1 deficiency HGNC:24945 Homo sapiens (human) 338328 GPIHBP1
  • RGD:7240710
DOID:0070266 congenital disorder of glycosylation type IIn HGNC:20862 Homo sapiens (human) 64116 SLC39A8
  • RGD:7240710
DOID:9870 galactosemia HGNC:24063 Homo sapiens (human) 130589 GALM
  • RGD:7240710
DOID:0112379 muscular dystrophy-dystroglycanopathy type B4 HGNC:3622 Homo sapiens (human) 2218 FKTN
  • RGD:7240710
DOID:2058 chronic mucocutaneous candidiasis HGNC:14558 Homo sapiens (human) 64581 CLEC7A
  • RGD:7240710
DOID:0050645 arterial tortuosity syndrome HGNC:13444 Homo sapiens (human) 81031 SLC2A10
  • RGD:7240710
DOID:14701 propionic acidemia HGNC:8654 Homo sapiens (human) 5096 PCCB
  • RGD:7240710
DOID:0080952 AMED syndrome HGNC:253 Homo sapiens (human) 128 ADH5
  • RGD:7240710
DOID:0111261 fumarase deficiency HGNC:3700 Homo sapiens (human) 2271 FH
  • RGD:7240710
DOID:0080470 developmental and epileptic encephalopathy 36 HGNC:30881 Homo sapiens (human) 79868 ALG13
  • RGD:7240710

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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: August 19, 2024