AL117258.1:Ensemblv90

leishmanolysin like peptidase 2
ClinGen, DECIPHER

7 panels

Panel Reviews Mode of inheritance Details
7 panels

Green AL117258.1 in Congenital Heart Defect


Level 2: Cardiovascular disorders
Version 0.511

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Heterotaxy, MONDO:0018677
  • congenital heart defects

Green AL117258.1 in Heterotaxy


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.44

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Heterotaxy, MONDO:0018677
  • congenital heart defects

Green AL117258.1 in Mendeliome


Version 1.3802

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Heterotaxy MONDO:0018677, congenital heart defects
Tags
  • new gene name

Green AL117258.1 in Fetal anomalies


Version 1.482

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Heterotaxy
  • congenital heart defects

Green AL117258.1 in Congenital Heart Defect


Level 2: Cardiovascular disorders
Version 1.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
  • Expert Review Green
Phenotypes
  • Heterotaxy, MONDO:0018677
  • congenital heart defects

Green AL117258.1 in Heterotaxy


Level 2: Dysmorphic and congenital abnormality syndromes
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
  • Expert Review Green
Phenotypes
  • Heterotaxy, MONDO:0018677
  • congenital heart defects

Green AL117258.1 in Fetal anomalies


Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
  • Expert Review Green
Phenotypes
  • Heterotaxy
  • congenital heart defects