FKBP8

FK506 binding protein 8
OMIM: 604840, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber FKBP8 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 6.181
Latest signed off version: v6.0 (30 Apr 2025)

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Spina bifida, HP:0002414
  • Vertebral segmentation defects