MEI4

meiotic double-stranded break formation protein 4
OMIM: 618417, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Green MEI4 in Mendeliome


Version 2.0

1 review BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Infertility disorder, MONDO:0005047, MEI4-related