long QT syndrome 2

Summary
Synonym
  • LQT2
Definition
A long QT syndrome that has_material_basis_in dominant inheritance of mutation in the KCNH2 gene on chromosome 7q36.1.
Super Class
autosomal dominant disease digenic disease long QT syndrome
Disease Ontology
DOID:0110645
Mondo Disease Ontology
MeSH
OMIM
GARD
Related Genes
Displaying all 3 entries
Gene ID Gene Symbol Description Source
3757 KCNH2 potassium voltage-gated channel subfamily H member 2
81033 KCNH6 potassium voltage-gated channel subfamily H member 6
144245 ALG10B ALG10 alpha-1,2-glucosyltransferase B
Displaying all 2 entries
Gene ID Gene Symbol Description Source
16511 Kcnh2 potassium voltage-gated channel, subfamily H (eag-related), member 2
380959 Alg10b ALG10 alpha-1,2-glucosyltransferase
Displaying all 2 entries
Gene ID Gene Symbol Description Source
117018 Kcnh2 potassium voltage-gated channel subfamily H member 2
245960 Alg10 ALG10, alpha-1,2-glucosyltransferase
Displaying 1 entry
Gene ID Gene Symbol Description Source
326193 Alg10 ALG10 alpha-1,2-glucosyltransferase
Displaying 1 entry
Gene ID Gene Symbol Description Source
100331575 alg10 ALG10 alpha-1,2-mannosyltransferase
Displaying 1 entry
Gene ID Gene Symbol Description Source Organism
548946 alg10 ALG10, alpha-1,2-glucosyltransferase Xenopus tropicalis (tropical clawed frog)
Displaying all 2 entries
Gene ID Gene Symbol Description Source
172855 algn-10 Dol-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-Dol alpha-1,2-glucosyltransferase
175527 unc-103 Cyclic nucleotide-binding domain-containing protein;Potassium voltage-gated channel unc-103
Displaying 1 entry
Gene ID Gene Symbol Description Source
853142 DIE2 dolichyl-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-dolichol alpha-1,2- glucosyltransferase
The Human Phenotype Ontology
Displaying all 10 entries
HPO ID HPO Term
HP:0001657 Prolonged QT interval
HP:0003581 Adult onset
HP:0001279 Syncope
HP:0011463 Childhood onset
HP:0001664 Torsade de pointes
HP:0000006 Autosomal dominant inheritance
HP:0001695 Cardiac arrest
HP:0001645 Sudden cardiac death
HP:0005184 Prolonged QTc interval
HP:0001663 Ventricular fibrillation
Displaying 1 entry
Gene ID Gene Symbol Description
144245 ALG10B ALG10 alpha-1,2-glucosyltransferase B

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Acknowledgements

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Last updated: December 9, 2024