1. Genes and Genomic Entities
  2. SLIT3

SLIT3

slit guidance ligand 3
OMIM: 603745, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Amber SLIT3 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 8.31
Latest signed off version: v8.0 (12 Aug 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • congenital anomalies of kidney and urinary tract 1 (MONDO:0019719)
  • congenital heart disease (MONDO:0005453)
  • congenital diaphragmatic hernia (MONDO:0005711)
Red SLIT3 in DDG2P


Version 8.2
Latest signed off version: v8.0 (12 Aug 2026)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • DD-Gene2Phenotype
    • Expert Review Red
    Phenotypes
    • SLIT3-related congenital anomalies
    Amber SLIT3 in Paediatric disorders - additional genes


    Level 2: Developmental disorders
    Version 8.27
    Latest signed off version: v8.8 (12 Aug 2026)

    Component of the following Super Panels:

  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • congenital anomalies of kidney and urinary tract 1 (MONDO:0019719)
    • congenital heart disease (MONDO:0005453)
    • congenital diaphragmatic hernia (MONDO:0005711)