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GTR Home > Conditions/Phenotypes > Preimplantation embryonic lethality 1

Summary

Maternal genes play a critical role in the very early stages of embryonic development because of the lag in transcribing genes derived from the male pronucleus. TLE6 mutations are a rare cause of human female-limited fertility and appear to represent the earliest known human embryonic lethality that is due to a single gene mutation. In affected women, ovulation proceeds normally and the retrieved oocytes appear normal, but zygote formation is severely impaired (Alazami et al., 2015). For a general phenotypic description and discussion of genetic heterogeneity of OZEMA, see 615774. [from OMIM]

Available tests

2 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Genes See tests for all associated and related genes

  • Also known as: GRG6, OZEMA15, PREMBL, TLE6
    Summary: TLE family member 6, subcortical maternal complex member

Clinical features

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