9d9r
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X-ray structure of ALX4 homeodomain dimer bound to DNA
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Structural highlights
DiseaseALX4_HUMAN Isolated scaphocephaly;Parietal foramina;Frontonasal dysplasia with alopecia and genital anomaly;Potocki-Shaffer syndrome. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. Disease susceptibility is associated with variations affecting the gene represented in this entry. FunctionALX4_HUMAN Transcription factor involved in skull and limb development. Plays an essential role in craniofacial development, skin and hair follicle development.[1] References
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This page was last modified 07:53, 9 April 2025.