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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 October 9, 2024
Displaying entries 70476 - 70500 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:112 esophageal varix HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:8664482
DOID:3908 lung non-small cell carcinoma HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:23778417
DOID:3525 middle cerebral artery infarction HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:22227456
DOID:783 end stage renal disease HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:11849406
DOID:1184 nephrotic syndrome HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:22203175
DOID:14525 Reye syndrome HGNC:399 Homo sapiens (human) 213 ALB
  • MGI:6194238
DOID:2855 hyperthyroxinemia HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:8048949
DOID:620 blood protein disease HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:20603593
DOID:4947 cholangiocarcinoma HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:10776430
  • PMID:17545000
  • PMID:20431764
DOID:11801 protein-energy malnutrition HGNC:399 Homo sapiens (human) 213 ALB
  • MGI:6194238
DOID:1168 familial hyperlipidemia HGNC:399 Homo sapiens (human) 213 ALB
  • MGI:6194238
DOID:552 pneumonia HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:23286966
DOID:6271 gastric cardia adenocarcinoma HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:15585392
DOID:8893 psoriasis HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:22607558
DOID:684 hepatocellular carcinoma HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:22392353
  • PMID:23892757
  • PMID:29040987
DOID:13576 twin-to-twin transfusion syndrome HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:23208016
DOID:5082 liver cirrhosis HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:23285146
DOID:6000 congestive heart failure HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:22158777
DOID:6432 pulmonary hypertension HGNC:396 Homo sapiens (human) 211 ALAS1
  • MGI:6194238
DOID:13268 porphyria HGNC:396 Homo sapiens (human) 211 ALAS1
  • MGI:6194238
DOID:13270 erythropoietic protoporphyria HGNC:396 Homo sapiens (human) 211 ALAS1
  • MGI:6194238
DOID:4450 renal cell carcinoma HGNC:393 Homo sapiens (human) 10000 AKT3
  • PMID:23378641
DOID:10283 prostate cancer HGNC:393 Homo sapiens (human) 10000 AKT3
  • PMID:22546513
DOID:4074 pancreatic adenocarcinoma HGNC:393 Homo sapiens (human) 10000 AKT3
  • PMID:27919956
DOID:1574 alcohol use disorder HGNC:393 Homo sapiens (human) 10000 AKT3
  • 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: December 9, 2024