IMMP2L

inner mitochondrial membrane peptidase subunit 2
OMIM: 605977, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red IMMP2L in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Autism

Red IMMP2L in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Genetic Health Queensland
Phenotypes
  • Autism