NR0B1

nuclear receptor subfamily 0 group B member 1
OMIM: 300473, Gene2Phenotype

8 panels

Panel Reviews Mode of inheritance Details
8 panels

Amber NR0B1 in Differences of Sex Development


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.293

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • 46XY sex reversal 2, dosage-sensitive, MIM# 300018
Tags
  • SV/CNV

Green NR0B1 in Mendeliome


Version 1.1891

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Adrenal hypoplasia, congenital (MIM# 300200)
  • 46XY sex reversal 2, dosage-sensitive, MIM# 300018
Tags
  • SV/CNV

Green NR0B1 in Mackenzie's Mission_Reproductive Carrier Screening


Level 2: Screening
Version 0.109

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • 46XY sex reversal 2, dosage-sensitive, 300018 (3)

Green NR0B1 in Additional findings_Paediatric


Level 2: Screening
Version 0.278

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • BabySeq Category A gene
  • Expert Review Green
Phenotypes
  • Congenital adrenal hypoplasia

Amber NR0B1 in Fetal anomalies


Version 1.255

review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Expert Review Amber
  • Genomics England PanelApp
Phenotypes
  • 46XY sex reversal 2, dosage-sensitive MIM#300018
Tags
  • SV/CNV

Green NR0B1 in Prepair 1000+


Level 2: Screening
Version 1.9

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • 46XY sex reversal 2, dosage-sensitive, 300018 (3)

Green NR0B1 in BabyScreen+ newborn screening


Level 2: Screening
Version 1.113

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • BabySeq Category A gene
Phenotypes
  • Adrenal hypoplasia, congenital (MIM# 300200)
Tags
  • treatable
  • endocrine

Green NR0B1 in Prepair 500+


Level 2: Screening
Version 1.1

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • 46XY sex reversal 2, dosage-sensitive, 300018 (3)