BNIP1

BCL2 interacting protein 1
OMIM: 603291, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber BNIP1 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 8.5
Latest signed off version: v8.0 (12 Aug 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
Phenotypes
  • Spondyloepiphyseal dysplasia, Holling type, OMIM:621345