1. Genes and Genomic Entities
  2. ZNF687

ZNF687

zinc finger protein 687
OMIM: 610568, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green ZNF687 in Skeletal dysplasia


Level 2: Musculoskeletal
Version 9.9
Latest signed off version: v9.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Research
    • Other
    Phenotypes
    • Paget disease of bone 6, OMIM:616833
    Red ZNF687 in Fetal anomalies


    Level 2: Fetal (including NIPD)
    Version 7.8
    Latest signed off version: v7.0 (6 May 2026)

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • NHS GMS
    Phenotypes
    • Paget disease of bone 6, OMIM:616833