Genomics England
GMS Panels
Panels
Genes and Entities
NCKAP1
NCK associated protein 1
OMIM:
604891
See this entity in PanelApp
Panel
Mode of inheritance
Details
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Intellectual disability
Component of the following Super Panels:
- Hypotonic infant
- Leukodystrophy, childhood onset
- Paediatric disorders
Signed-off version 11.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Intellectual disability, Autism