LEF1

lymphoid enhancer binding factor 1
OMIM: 153245, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green LEF1 in Mendeliome


Version 1.1902

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Syndromic disease, MONDO:0002254, LEF1-related

Red LEF1 in Oligodontia


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.29

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
  • Expert Review Red
  • Literature
Phenotypes
  • Ectodermal dysplasia, no OMIM# yet

Green LEF1 in Polydactyly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.276

Component of the following Super Panels:

  • Limb and Digital Malformations SuperPanel
  • review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Syndromic disease, MONDO:0002254, LEF1-related

    Green LEF1 in Radial Ray Abnormalities


    Level 2: Dysmorphic and congenital abnormality syndromes
    Version 1.10

    Component of the following Super Panels:

  • Limb and Digital Malformations SuperPanel
  • review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Syndromic disease, MONDO:0002254, LEF1-related

    Green LEF1 in Ectodermal Dysplasia


    Level 2: Dermatological disorders
    Version 0.86

    review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    • Literature
    Phenotypes
    • Syndromic disease, MONDO:0002254, LEF1-related