PTK7

protein tyrosine kinase 7 (inactive)
OMIM: 601890, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red PTK7 in Familial Neural Tube Defects


Version 1.10

review Not set
Sources
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Neural tube defects
Red PTK7 in Autism


Version 0.36

review Not set
Sources
  • Expert Review Red
  • SFARI
Red PTK7 in Monogenic hearing loss

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 4.36
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

  • Paediatric disorders
  • review Not set
    Sources
    • Expert