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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 7176 - 7200 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:0050793 short QT syndrome HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • RGD:7240710
DOID:0050650 familial atrial fibrillation HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • RGD:7240710
DOID:4440 seminoma HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • PMID:15389592
DOID:10763 hypertension HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • MGI:6194238
DOID:0110644 long QT syndrome 1 HGNC:6294 Homo sapiens (human) 3784 KCNQ1
  • MGI:6194238
  • RGD:7240710
DOID:9351 diabetes mellitus HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • PMID:15292329
DOID:0070218 familial hyperinsulinemic hypoglycemia 2 HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • MGI:6194238
  • PMID:17259403
  • PMID:19498446
  • PMID:19502414
  • RGD:7240710
DOID:10763 hypertension HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • MGI:6194238
DOID:0060639 permanent neonatal diabetes mellitus HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • PMID:15115830
  • PMID:16670688
  • RGD:7240710
DOID:11716 prediabetes syndrome HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • MGI:6194238
DOID:11446 sciatic neuropathy HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • MGI:6194238
DOID:11832 visual epilepsy HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • MGI:6194238
DOID:2018 hyperinsulinism HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • PMID:15998776
DOID:1824 status epilepticus HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • MGI:6194238
DOID:0080855 Parkinsonism HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • MGI:6194238
DOID:0111110 maturity-onset diabetes of the young type 13 HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • RGD:7240710
DOID:114 heart disease HGNC:8638 Homo sapiens (human) 8850 KAT2B
  • MGI:6194238
DOID:3748 esophagus squamous cell carcinoma HGNC:8638 Homo sapiens (human) 8850 KAT2B
  • PMID:19525977
DOID:7148 rheumatoid arthritis HGNC:8638 Homo sapiens (human) 8850 KAT2B
  • PMID:36104638
DOID:684 hepatocellular carcinoma HGNC:8638 Homo sapiens (human) 8850 KAT2B
  • PMID:23643089
DOID:1612 breast cancer HGNC:8638 Homo sapiens (human) 8850 KAT2B
  • PMID:22199269
DOID:557 kidney disease HGNC:8638 Homo sapiens (human) 8850 KAT2B
  • MGI:6194238
DOID:557 kidney disease HGNC:4201 Homo sapiens (human) 2648 KAT2A
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma HGNC:4201 Homo sapiens (human) 2648 KAT2A
  • PMID:23543735

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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