AMOTL1

angiomotin like 1
OMIM: 614657, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green AMOTL1 in Congenital Heart Defect


Level 2: Cardiovascular disorders
Version 0.430

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Orofacial clefting syndrome, MONDO:0015335, AMOTL1-related

Green AMOTL1 in Mendeliome


Version 1.2374

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Orofacial clefting syndrome, MONDO:0015335, AMOTL1 -related

Green AMOTL1 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.83

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Orofacial clefting syndrome, MONDO:0015335, AMOTL1-related

Green AMOTL1 in Clefting disorders

Level 3: Dysmorphic disorders
Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.260

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Orofacial clefting syndrome, MONDO:0015335, AMOTL1 -related

Green AMOTL1 in Fetal anomalies


Version 1.314

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Orofacial clefting syndrome, MONDO:0015335, AMOTL1-related