1. Genes and Genomic Entities
  2. CMIP

CMIP

c-Maf inducing protein
OMIM: 610112, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Amber CMIP in Autism


Version 0.36

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • SFARI
Phenotypes
  • HP:0012759
  • HP:0000717
  • HP:0007018
  • HP:0001250
  • HP:0011471
Red CMIP in Intellectual disability - microarray and sequencing

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 5.531
Latest signed off version: v5.0 (22 Mar 2023)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Other
    Phenotypes
    • HP:0012759
    • HP:0000717
    • HP:0007018
    • HP:0001250
    • HP:0011471