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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 5401 - 5425 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence Code Names References
DOID:3908 lung non-small cell carcinoma HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:11389090
DOID:0014667 disease of metabolism SGD:S000000036 Saccharomyces cerevisiae S288C 851193 CDC19
  • MGI:6194238
DOID:6000 congestive heart failure SGD:S000005486 Saccharomyces cerevisiae S288C 853994 MDH2
  • MGI:6194238
DOID:4194 glucose metabolism disease MGI:96103 Mus musculus (house mouse) 15275 Hk1
  • MGI:6194238
DOID:10763 hypertension ZFIN:ZDB-GENE-080402-11 Danio rerio (zebrafish) 563897 gbgt1l5
  • MGI:6194238
DOID:5016 hepatocellular clear cell carcinoma HGNC:6554 Homo sapiens (human) 3953 LEPR
  • PMID:20723213
DOID:3525 middle cerebral artery infarction HGNC:18129 Homo sapiens (human) 51738 GHRL
  • MGI:6194238
DOID:4137 common bile duct disease HGNC:10982 Homo sapiens (human) 8604 SLC25A12
  • MGI:6194238
DOID:0070262 congenital disorder of glycosylation type IIj HGNC:18620 Homo sapiens (human) 25839 COG4
  • RGD:7240710
DOID:14115 toxic shock syndrome SGD:S000004942 Saccharomyces cerevisiae S288C 855373 ERR3
  • MGI:6194238
DOID:2596 larynx cancer HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:23516596
DOID:2747 glycogen storage disease HGNC:9386 Homo sapiens (human) 51422 PRKAG2
  • PMID:15877279
DOID:9452 steatotic liver disease HGNC:12518 Homo sapiens (human) 7351 UCP2
  • MGI:6194238
DOID:4195 hyperglycemia RGD:2670 Rattus norvegicus (Norway rat) 24385 Gck
  • MGI:6194238
DOID:0050866 oral squamous cell carcinoma RGD:70982 Rattus norvegicus (Norway rat) 84027 Gsk3b
  • MGI:6194238
DOID:10763 hypertension MGI:1096330 Mus musculus (house mouse) 12015 Bad
  • MGI:6194238
DOID:10825 essential hypertension HGNC:5208 Homo sapiens (human) 3290 HSD11B1
  • PMID:26671915
DOID:9970 obesity MGI:97583 Mus musculus (house mouse) 18708 Pik3r1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus RGD:621503 Rattus norvegicus (Norway rat) 84020 Kcnq1
  • MGI:6194238
DOID:0014667 disease of metabolism MGI:97547 Mus musculus (house mouse) 18641 Pfkl
  • MGI:6194238
DOID:0070254 congenital disorder of glycosylation type IIb WB:WBGene00008775 Caenorhabditis elegans 177998 mogs-1
  • MGI:6194238
DOID:0080630 B-lymphoblastic leukemia/lymphoma SGD:S000005646 Saccharomyces cerevisiae S288C 854287 GCY1
  • MGI:6194238
DOID:2986 IgA glomerulonephritis HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:12566518
DOID:1495 cystic echinococcosis MGI:96824 Mus musculus (house mouse) 21898 Tlr4
  • MGI:6194238
DOID:0111141 delayed sleep phase syndrome MGI:1270841 Mus musculus (house mouse) 12952 Cry1
  • 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