PJA1

praja ring finger ubiquitin ligase 1
OMIM: 300420, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Amber PJA1 in Craniosynostosis


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.73

1 review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • X-linked complex neurodevelopmental disorder, PJA1-related, MONDO:0100148
Tags
  • founder

Amber PJA1 in Mendeliome


Version 1.3795

2 reviews X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • X-linked complex neurodevelopmental disorder, PJA1-related, MONDO:0100148

Amber PJA1 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.507

1 review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • X-linked complex neurodevelopmental disorder, PJA1-related, MONDO:0100148
Tags
  • founder

Amber PJA1 in Fetal anomalies


Version 1.482

2 reviews X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • X-linked complex neurodevelopmental disorder, PJA1-related, MONDO:0100148