RecName: Full=Transcription factor 20; Short=TCF-20; AltName: Full=Nuc - Protein

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Diagnosis and clinical presentation of two individuals with a rare TCF20 pathogenic variant. [BMJ Case Rep. 2022]
Diagnosis and clinical presentation of two individuals with a rare TCF20 pathogenic variant.
Schneeweiss MR, Dale B, Ejaz R. BMJ Case Rep. 2022 Dec 7; 15(12). Epub 2022 Dec 7.
Rare and de novo duplications containing TCF20 are associated with a neurodevelopmental disorder. [Clin Genet. 2022]
Rare and de novo duplications containing TCF20 are associated with a neurodevelopmental disorder.
Lévy J, Cogan G, Maruani A, Maillard A, Dupont C, Drunat S, Rachid M, Atzori P, Delorme R, Jeyarajah S, et al. Clin Genet. 2022 Mar; 101(3):364-370. Epub 2021 Dec 28.
De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome. [Genome Med. 2019]
De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome.
Vetrini F, McKee S, Rosenfeld JA, Suri M, Lewis AM, Nugent KM, Roeder E, Littlejohn RO, Holder S, Zhu W, et al. Genome Med. 2019 Feb 28; 11(1):12. Epub 2019 Feb 28.

RefSeq genomic sequence
See the genomic reference sequence for the TCF20 gene (NG_028982.3).
RefSeq protein isoforms
See 17 reference sequence protein isoforms for the TCF20 gene.

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Q9UGU0 [Domain Mapping of Disease Mut...]
Q9UGU0
Domain Mapping of Disease Mutations
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Protein