ISL1

ISL LIM homeobox 1
OMIM: 600366, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red ISL1 in CAKUT

Level 3: Structural renal and urinary tract disease
Level 2: Renal and urinary tract disorders
Version 1.181

review Unknown
Sources
  • Literature
Phenotypes
  • CAKUT
Amber ISL1 in Paediatric disorders - additional genes


Level 2: Developmental disorders
Version 7.31
Latest signed off version: v7.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • ClinGen
    Phenotypes
    • congenital heart disease, MONDO:0005453
    Tags
    • Q3_25_promote_green