PanelApp (stage)
  1. Genes and Genomic Entities
  2. NXN

NXN

nucleoredoxin
OMIM: 612895, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green NXN in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Robinow syndrome, autosomal recessive 2 618529

Green NXN in Hand and foot malformations


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.74

Component of the following Super Panels:

  • Limb and Digital Malformations SuperPanel

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    • Victorian Clinical Genetics Services
    Phenotypes
    • Robinow syndrome, autosomal recessive 2 MIM#618529

    Green NXN in Fetal anomalies


    Version 1.255

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Robinow syndrome, autosomal recessive 2, OMIM:618529
    • Robinow syndrome, autosomal recessive 2, MONDO:0032800