PanelApp (staging)
  1. Genes and Genomic Entities
  2. SECISBP2

SECISBP2

SECIS binding protein 2
OMIM: 607693, ClinGen, DECIPHER

7 panels

Panel Reviews Mode of inheritance Details
7 panels

Green SECISBP2 in Mendeliome


Version 1.2302

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Thyroid hormone metabolism, abnormal, MIM# 609698

Green SECISBP2 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.108

Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Thyroid hormone metabolism, abnormal, 1, MIM# 609698

    Green SECISBP2 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.63

    		2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Thyroid hormone metabolism, abnormal, 1, MIM# 609698

    Green SECISBP2 in Hyperthyroidism


    Level 2: Endocrine disorders
    Version 0.23

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Thyroid hormone metabolism, abnormal, MIM# 609698

    Green SECISBP2 in Metal Metabolism Disorders


    Level 2: Metabolic disorders
    Version 0.45

    Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions

    		•  0 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    Phenotypes
    • thyroid hormone metabolism, abnormal 1 MONDO:0800046
    • Other disorders of trace element metabolism

    Green SECISBP2 in Congenital hypothyroidism

    Level 3: Thyroid disorders
    Level 2: Endocrine disorders
    Version 0.43

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Thyroid hormone metabolism, abnormal, MIM# 609698

    Red SECISBP2 in Fetal anomalies


    Version 1.313

    		2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Genomics England PanelApp
    • Literature
    Phenotypes
    • Thyroid hormone metabolism, abnormal, MIM# 609698