LHX4 Polyclonal Antibody, 50ul Pipette Filler Mutations in this gene are

Mutations in this gene are associated with Noonan syndrome 5 and LEOPARD syndrome 2

5 mm Narrow Blade

Alternatively spliced transcript variants have been reported| but the full-length nature of these variants has not been determined

This gene is located in the cystatin locus and encodes a secreted protein that may play a role in hematopoietic differentiation or inflammation

This gene encodes a 28S subunit protein that belongs to the ribosomal protein S21P family

LHX4 Polyclonal Antibody, 50ul Pipette Filler Mutations in this gene areThis 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.