From Infogalactic: the planetary knowledge core
Bamforth–Lazarus syndrome is a genetic condition that results in thyroid dysgenesis.[1][2] It is due to recessive mutations in forkhead/winged-helix domain transcription factor (FKLH15 or TTF2).[3]
It is associated with FOXE1.[4]
References
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(1) Basic domains |
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(2) Zinc finger
DNA-binding domains |
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(3) Helix-turn-helix domains |
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(4) β-Scaffold factors
with minor groove contacts |
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(0) Other transcription factors |
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Ungrouped |
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Transcription coregulators |
Coactivator: |
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Corepressor: |
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