NRIP1

nuclear receptor interacting protein 1
OMIM: 602490, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber NRIP1 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 8.26
Latest signed off version: v8.0 (12 Aug 2026)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • NHS GMS
  • Expert Review Amber
Phenotypes
  • Congenital anomalies of kidney and urinary tract 3, OMIM:618270
  • congenital anomalies of kidney and urinary tract 3, MONDO:0032646