ATRIP

ATR interacting protein
OMIM: 606605, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Red ATRIP in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Seckel Syndrome, MONDO:0019342, ATRIP-related

Red ATRIP in Microcephaly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.269

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Seckel Syndrome

Red ATRIP in Growth failure


Version 1.76

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Genomics England PanelApp
Phenotypes
  • Seckel-like syndrome

Red ATRIP in Fetal anomalies


Version 1.255

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Seckel Syndrome