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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 1401 - 1425 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9352 type 2 diabetes mellitus WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:557 kidney disease WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:9281 phenylketonuria WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:2355 anemia WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:583 hemolytic anemia WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:6713 cerebrovascular disease WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:9970 obesity WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:13413 hepatic encephalopathy WB:WBGene00007108 Caenorhabditis elegans 178046 gspd-1
  • MGI:6194238
DOID:0110645 long QT syndrome 2 WB:WBGene00007043 Caenorhabditis elegans 172855 algn-10
  • MGI:6194238
DOID:0050563 nonsyndromic deafness WB:WBGene00007043 Caenorhabditis elegans 172855 algn-10
  • MGI:6194238
DOID:0050579 glycogen storage disease XV WB:WBGene00006863 Caenorhabditis elegans 180644 gyg-1
  • MGI:6194238
DOID:332 amyotrophic lateral sclerosis WB:WBGene00006575 Caenorhabditis elegans 175502 tir-1
  • PMID:26059317
DOID:1289 neurodegenerative disease WB:WBGene00006575 Caenorhabditis elegans 175502 tir-1
  • MGI:6194238
DOID:0080575 Larsen-like syndrome B3GAT3 type WB:WBGene00005026 Caenorhabditis elegans 174517 sqv-8
  • MGI:6194238
DOID:9206 Barrett's esophagus WB:WBGene00005026 Caenorhabditis elegans 174517 sqv-8
  • MGI:6194238
DOID:5419 schizophrenia WB:WBGene00005026 Caenorhabditis elegans 174517 sqv-8
  • MGI:6194238
DOID:3770 pulmonary fibrosis WB:WBGene00005026 Caenorhabditis elegans 174517 sqv-8
  • MGI:6194238
DOID:0050775 schneckenbecken dysplasia WB:WBGene00005025 Caenorhabditis elegans 174145 sqv-7
  • MGI:6194238
DOID:2738 pseudoxanthoma elasticum WB:WBGene00005024 Caenorhabditis elegans 190099 sqv-6
  • MGI:6194238
DOID:0060462 Desbuquois dysplasia WB:WBGene00005024 Caenorhabditis elegans 190099 sqv-6
  • MGI:6194238
DOID:557 kidney disease WB:WBGene00005024 Caenorhabditis elegans 190099 sqv-6
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus WB:WBGene00005024 Caenorhabditis elegans 190099 sqv-6
  • MGI:6194238
DOID:0080322 polycystic kidney disease WB:WBGene00005024 Caenorhabditis elegans 190099 sqv-6
  • MGI:6194238

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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