KLC1

kinesin light chain 1
OMIM: 600025, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green KLC1 in Mendeliome


Version 2.268

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • KLC1-related neurodevelopmental disorder, MONDO:0700092

Green KLC1 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 2.41

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
  • Literature
Phenotypes
  • KLC1-related neurodevelopmental disorder, MONDO:0700092

Green KLC1 in Dystonia and Chorea


Level 2: Neurology and neurodevelopmental disorders
Version 1.5

Component of the following Super Panels:

  • Movement Disorders Superpanel
  • Progressive Neurological Conditions
  • 1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    • Literature
    Phenotypes
    • KLC1-related neurodevelopmental disorder, MONDO:0700092