PanelApp
  1. Genes and Genomic Entities
  2. ZMYM2

ZMYM2

zinc finger MYM-type containing 2
OMIM: 602221, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green ZMYM2 in Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic


Level 2: Renal and urinary tract disorders
Version 0.159

Component of the following Super Panels:

  • Congenital abnormalities of the kidneys and urinary tract (CAKUT)_SuperPanel
  • Kidneyome_SuperPanel

    		•  2 reviews MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities, MIM# 619522

    Red ZMYM2 in Cerebral Palsy


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.400

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities, MIM#619522

    Green ZMYM2 in Congenital Heart Defect


    Level 2: Cardiovascular disorders
    Version 0.474

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert Review
    Phenotypes
    • Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities, MIM# 619522

    Green ZMYM2 in Mendeliome


    Version 1.3512

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Congenital anomalies of kidney and urinary tract
    • Neurodevelopmental disorder

    Green ZMYM2 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.410

    		2 reviews MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities, MIM# 619522

    Green ZMYM2 in Fetal anomalies


    Version 1.465

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    • Expert list
    Phenotypes
    • Neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities - MIM#619522