PanelApp (stage)
  1. Genes and Genomic Entities
  2. TMEM260

TMEM260

transmembrane protein 260
OMIM: 617449, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green TMEM260 in Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic


Level 2: Renal and urinary tract disorders
Version 0.138

Component of the following Super Panels:

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

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review
    Phenotypes
    • Structural heart defects and renal anomalies syndrome, MIM# 617478

    Green TMEM260 in Congenital Heart Defect


    Level 2: Cardiovascular disorders
    Version 0.418

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Structural heart defects and renal anomalies syndrome, MIM# 617478

    Green TMEM260 in Mendeliome


    Version 1.1891

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Structural heart defects and renal anomalies syndrome, MIM# 617478

    Red TMEM260 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Genetic Health Queensland
    Phenotypes
    • Structural heart defects and renal anomalies syndrome, MIM# 617478

    Green TMEM260 in Fetal anomalies


    Version 1.255

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    • Genetic Health Queensland
    Phenotypes
    • Structural heart defects and renal anomalies syndrome, OMIM:617478
    • Structural heart defects and renal anomalies syndrome, MONDO:0044321