OBO ID: DOID:0110645
Term Name: long QT syndrome 2 Search Ontology:
Synonyms:
  • LQT2
Definition: A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNH2 gene on chromosome 7q36.1. https://www.ncbi.nlm.nih.gov/pubmed/7889573
References:
Ontology: Human Disease   (DOID:0110645)
OTHER long QT syndrome 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ALG10 {Long QT syndrome, acquired, reduced susceptibility to} 613688
ALG10B {Long QT syndrome, acquired, reduced susceptibility to} 613688
KCNH2 Long QT syndrome 2 613688
{Long QT syndrome 2, acquired, susceptibility to} 613688
ZEBRAFISH MODELS
Fish Conditions Citations
nkhspGFF3AEt + MO1-kcnh6a standard conditions Tanaka et al., 2018
PHENOTYPE No data available

CITATIONS (1)