1. Genes and Genomic Entities
  2. NCAPD3

NCAPD3

non-SMC condensin II complex subunit D3
OMIM: 609276, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green NCAPD3 in Severe microcephaly

Level 3: DNA repair disorders
Level 2: Dysmorphic and congenital abnormality syndromes
Version 5.7
Latest signed off version: v5.0 (1 May 2024)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review Green
  • Literature
Phenotypes
  • Microcephaly 22, primary, autosomal recessive, OMIM:617984
Red NCAPD3 in DDG2P


Version 4.3
Latest signed off version: v4.0 (1 May 2024)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • DD-Gene2Phenotype
    • Expert Review Red
    Phenotypes
    • Microcephaly with short stature