SPEF2

sperm flagellar 2
OMIM: 610172, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Amber SPEF2 in Ciliary Dyskinesia


Level 2: Respiratory disorders
Version 1.52

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Spermatogenic failure 43, MIM#618751
  • Primary ciliary dyskinesia-like phenotype

Green SPEF2 in Mendeliome


Version 1.2789

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Spermatogenic failure 43, MIM#618751
  • Spermatogenic failure 43, MIM#618751
  • Primary ciliary dyskinesia-like phenotype

Red SPEF2 in Fetal anomalies


Version 1.378

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Spermatogenic failure 43, MIM#618751
  • Primary ciliary dyskinesia-like phenotype

Green SPEF2 in Infertility and Recurrent Pregnancy Loss


Version 1.7

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Spermatogenic failure 43, MIM# 618751