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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 4801 - 4825 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:783 end stage renal disease HGNC:6522 Homo sapiens (human) 3931 LCAT
  • MGI:6194238
DOID:1391 Norum disease HGNC:6522 Homo sapiens (human) 3931 LCAT
  • MGI:6194238
  • PMID:16061733
  • RGD:7240710
DOID:1168 familial hyperlipidemia HGNC:6522 Homo sapiens (human) 3931 LCAT
  • MGI:6194238
DOID:0111646 congenital lactase deficiency HGNC:6530 Homo sapiens (human) 3938 LCT
  • RGD:7240710
DOID:557 kidney disease HGNC:6530 Homo sapiens (human) 3938 LCT
  • MGI:6194238
DOID:0060180 colitis HGNC:6530 Homo sapiens (human) 3938 LCT
  • MGI:6194238
DOID:13250 diarrhea HGNC:6530 Homo sapiens (human) 3938 LCT
  • MGI:6194238
DOID:10763 hypertension HGNC:6535 Homo sapiens (human) 3939 LDHA
  • MGI:6194238
DOID:0014667 disease of metabolism HGNC:6535 Homo sapiens (human) 3939 LDHA
  • MGI:6194238
DOID:4195 hyperglycemia HGNC:6535 Homo sapiens (human) 3939 LDHA
  • MGI:6194238
DOID:0014667 disease of metabolism HGNC:6541 Homo sapiens (human) 3945 LDHB
  • MGI:6194238
DOID:0014667 disease of metabolism HGNC:6544 Homo sapiens (human) 3948 LDHC
  • MGI:6194238
DOID:0070259 congenital disorder of glycosylation type IIg HGNC:6545 Homo sapiens (human) 9382 COG1
  • RGD:7240710
DOID:0070269 congenital disorder of glycosylation type IIq HGNC:6546 Homo sapiens (human) 22796 COG2
  • RGD:7240710
DOID:2018 hyperinsulinism HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
DOID:0050741 alcohol dependence HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
  • PMID:29912265
DOID:5016 hepatocellular clear cell carcinoma HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:20723213
DOID:783 end stage renal disease HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:9294834
DOID:0111334 congenital leptin deficiency HGNC:6553 Homo sapiens (human) 3952 LEP
  • RGD:7240710
DOID:0050848 obstructive sleep apnea HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:18606530
DOID:3083 chronic obstructive pulmonary disease HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:20021311
  • PMID:20854423
  • PMID:21367591
DOID:12236 primary biliary cholangitis HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:16093869
DOID:11714 gestational diabetes HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:19269197
DOID:4483 rhinitis HGNC:6553 Homo sapiens (human) 3952 LEP
  • PMID:19860581
DOID:684 hepatocellular carcinoma HGNC:6553 Homo sapiens (human) 3952 LEP
  • MGI:6194238
  • PMID:18573568
  • PMID:28452232

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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