rs565803862

This variant is located in the LHX4 gene.

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ClinVar annotation

Likely Benign★☆☆☆

1 submitter

Short stature-pituitary and cerebellar defects-small sella turcica syndrome

About LHX4

This gene encodes a member of a large protein family which contains the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein is a transcription factor involved in the control of differentiation and development of the pituitary gland. Mutations in this gene cause combined pituitary hormone deficiency 4. [provided by RefSeq, Dec 2010]

View all LHX4 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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