9kh2
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Crystal structure of the first three zinc finger domains of ZBTB20 in complex with DNA
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Structural highlights
DiseaseZBT20_HUMAN Intellectual disability-cataracts-calcified pinnae-myopathy syndrome. The disease is caused by variants affecting the gene represented in this entry. FunctionZBT20_HUMAN May be a transcription factor that may be involved in hematopoiesis, oncogenesis, and immune responses (PubMed:11352661). Plays a role in postnatal myogenesis, may be involved in the regulation of satellite cells self-renewal (By similarity).[UniProtKB:Q8K0L9][1] References
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This page was last modified 06:22, 26 November 2025.