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簡(jiǎn)要描述：The protein encoded by this gene is a transcription factor that contains both basic helix-loop-helix and leucine zipper structural features. The encoded protein regulates melanocyte development and is responsible for pigment cell-specific transcription of the melanogenesis enzyme genes. Heterozygous mutations in the this gene cause auditory-pigmentary syndromes, such as Waardenburg syndrome type 2 and Tietz syndrome. [provided by RefSeq, Aug 2017]
產(chǎn)品型號(hào)：bsm-63195R廠商性質(zhì)：生產(chǎn)廠家更新時(shí)間：2025-03-05訪 問(wèn) 量： 215產(chǎn)品分類
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