1. Genes and Genomic Entities
  2. ZNF865

ZNF865

zinc finger protein 865
Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
No list ZNF865 in Ataxia and cerebellar anomalies - narrow panel


Level 2: Neurology
Version 9.1
Latest signed off version: v9.0 (6 May 2026)

Component of the following Super Panels:

  • Hereditary ataxia and cerebellar anomalies - childhood onset

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Removed
    • Literature
    Phenotypes
    • neurodevelopmental disorder, MONDO:0700092
    Tags
    • curated_removed
    Amber ZNF865 in Malformations of cortical development


    Level 2: Neurology
    Version 8.1
    Latest signed off version: v8.0 (6 May 2026)

    Component of the following Super Panels:

  • Cerebral malformation
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • neurodevelopmental disorder, MONDO:0700092
    Tags
    • Q1_26_promote_green
    Amber ZNF865 in Fetal anomalies


    Level 2: Fetal (including NIPD)
    Version 7.5
    Latest signed off version: v7.0 (6 May 2026)

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • neurodevelopmental disorder, MONDO:0700092
    Tags
    • Q1_26_promote_green
    Amber ZNF865 in Intellectual disability


    Level 2: Developmental disorders
    Version 10.11
    Latest signed off version: v10.0 (6 May 2026)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • neurodevelopmental disorder, MONDO:0700092
    Tags
    • Q4_25_promote_green