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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 11751 - 11775 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:0080322 polycystic kidney disease SGD:S000006148 Saccharomyces cerevisiae S288C 855874 ALG5
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I SGD:S000006148 Saccharomyces cerevisiae S288C 855874 ALG5
  • PMID:10359825
DOID:0080322 polycystic kidney disease HGNC:20266 Homo sapiens (human) 29880 ALG5
  • RGD:7240710
DOID:0080556 congenital disorder of glycosylation Id SGD:S000000178 Saccharomyces cerevisiae S288C 852196 ALG3
  • MGI:6194238
  • PMID:23038983
DOID:5212 congenital disorder of glycosylation HGNC:23056 Homo sapiens (human) 10195 ALG3
  • MGI:6194238
DOID:0080556 congenital disorder of glycosylation Id HGNC:23056 Homo sapiens (human) 10195 ALG3
  • MGI:6194238
  • RGD:7240710
DOID:5212 congenital disorder of glycosylation SGD:S000000178 Saccharomyces cerevisiae S288C 852196 ALG3
  • PMID:10581255
DOID:0080561 congenital disorder of glycosylation Ii SGD:S000003033 Saccharomyces cerevisiae S288C 852815 ALG2
  • MGI:6194238
DOID:0110669 congenital myasthenic syndrome 14 SGD:S000003033 Saccharomyces cerevisiae S288C 852815 ALG2
  • MGI:6194238
DOID:0080561 congenital disorder of glycosylation Ii HGNC:23159 Homo sapiens (human) 85365 ALG2
  • RGD:7240710
DOID:0110669 congenital myasthenic syndrome 14 HGNC:23159 Homo sapiens (human) 85365 ALG2
  • RGD:7240710
DOID:0080563 congenital disorder of glycosylation Ik HGNC:37258 Homo sapiens (human) 644974 ALG1L2
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation HGNC:37258 Homo sapiens (human) 644974 ALG1L2
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I HGNC:37258 Homo sapiens (human) 644974 ALG1L2
  • MGI:6194238
DOID:0110658 congenital myasthenic syndrome 15 SGD:S000000274 Saccharomyces cerevisiae S288C 852362 ALG14
  • MGI:6194238
DOID:0110658 congenital myasthenic syndrome 15 HGNC:28287 Homo sapiens (human) 199857 ALG14
  • RGD:7240710
DOID:0080470 developmental and epileptic encephalopathy 36 HGNC:30881 Homo sapiens (human) 79868 ALG13
  • RGD:7240710
DOID:0080470 developmental and epileptic encephalopathy 36 SGD:S000003015 Saccharomyces cerevisiae S288C 852835 ALG13
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I HGNC:19358 Homo sapiens (human) 79087 ALG12
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I SGD:S000005313 Saccharomyces cerevisiae S288C 855764 ALG12
  • PMID:12217961
DOID:0080559 congenital disorder of glycosylation Ig HGNC:19358 Homo sapiens (human) 79087 ALG12
  • RGD:7240710
DOID:0080559 congenital disorder of glycosylation Ig SGD:S000005313 Saccharomyces cerevisiae S288C 855764 ALG12
  • MGI:6194238
DOID:0080567 congenital disorder of glycosylation Ip HGNC:32456 Homo sapiens (human) 440138 ALG11
  • RGD:7240710
DOID:0080567 congenital disorder of glycosylation Ip SGD:S000004993 Saccharomyces cerevisiae S288C 855679 ALG11
  • MGI:6194238
DOID:0110645 long QT syndrome 2 HGNC:31088 Homo sapiens (human) 144245 ALG10B
  • RGD:7240710

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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