联系人 Ms. Emily
45-1 Ramsey Road, Shirley, New York
This intronless gene belongs to the forkhead family of
transcription factors, which is characterized by a distinct
forkhead domain. This gene functions as a thyroid transcription
factor which likely plays a crucial role in thyroid morphogenesis.
Mutations in this gene are associated with congenital
hypothyroidism and cleft palate with thyroid dysgenesis. The map
localization of this gene suggests it may also be a candidate gene
for squamous cell epithelioma and hereditary sensory neuropathy
type I.
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