5hod | pdb_00005hod
From Proteopedia
Structure of LHX4 transcription factor complexed with DNA
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Structural highlights
Disease[LHX4_HUMAN] Hypothyroidism due to deficient transcription factors involved in pituitary development or function;Pituitary stalk interruption syndrome;Short stature - pituitary and cerebellar defects - small sella turcica. The disease is caused by mutations affecting the gene represented in this entry. A chromosomal aberration involving LHX4 may be a cause of acute lymphoblastic leukemia. Translocation t(1;14)(q25;q32) with IGHG1.[1] Function[LHX4_HUMAN] May play a critical role in the development of respiratory control mechanisms and in the normal growth and maturation of the lung. References | ||||||||||||||||
This page was last modified 18:04, 1 February 2017.