TTL:Ensemblv115

tubulin tyrosine ligase
OMIM: 608291, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber TTL in Tubulinopathies


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Other
  • Expert Review Amber
Phenotypes
  • complex neurodevelopmental disorder MONDO:0100038

Red TTL in Hypertrophic cardiomyopathy_HCM


Level 2: Cardiovascular disorders
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Literature
  • Expert Review Red
Phenotypes
  • Hypertrophic cardiomyopathy, MONDO:0005045, TTL-related