1. Genes and Genomic Entities
  2. SIN3B

SIN3B

SIN3 transcription regulator family member B
OMIM: 607777, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red SIN3B in DDG2P


Version 6.447
Latest signed off version: v6.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Red
    • DD-Gene2Phenotype
    Phenotypes
    • SIN3B-related syndromic intellectual disability and autism spectrum disorder
    Green SIN3B in Intellectual disability


    Level 2: Developmental disorders
    Version 9.397
    Latest signed off version: v9.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Syndromic intellectual disability
    Tags
    • gene-checked