KALRN

kalirin RhoGEF kinase
OMIM: 604605, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red KALRN in Mendeliome


Version 1.4215

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Coronary artery disorder MONDO:0005010, KALRN-related
  • Intellectual disability (MONDO:0001071), KALRN-related