PanelApp
  1. Genes and Genomic Entities
  2. KLC4

KLC4

kinesin light chain 4
Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red KLC4 in Mendeliome


Version 1.3512

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Expert Review
Phenotypes
  • Complicated hereditary spastic paraplegia

Red KLC4 in Regression


Level 2: Neurology and neurodevelopmental disorders
Version 0.594

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Neurodegeneration, early-childhood-onset, with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy, MIM# 621129

Red KLC4 in Hereditary Spastic Paraplegia - paediatric


Level 2: Neurology and neurodevelopmental disorders
Version 1.102

Component of the following Super Panels:

  • Hereditary Spastic Paraplegia Superpanel
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Royal Melbourne Hospital
    Phenotypes
    • spastic paraplegia
    • progressive complicated spastic paraplegia