Homo sapiens HNF-3beta mRNA for hepatocyte nuclear factor-3 beta, comp - Nucleotide

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Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements. [Eur J Hum Genet. 2024]
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements.
Laver TW, Wakeling MN, Caswell RC, Bunce B, Yau D, Männistö JME, Houghton JAL, Hopkins JJ, Weedon MN, Saraff V, et al. Eur J Hum Genet. 2024 Jul; 32(7):813-818. Epub 2024 Apr 11.
FOXA2-initiated transcriptional activation of INHBA induced by methylmalonic acid promotes pancreatic neuroendocrine neoplasm progression. [Cell Mol Life Sci. 2024]
FOXA2-initiated transcriptional activation of INHBA induced by methylmalonic acid promotes pancreatic neuroendocrine neoplasm progression.
Hu C, Ye M, Bai J, Liu P, Lu F, Chen J, Xu Y, Yan L, Yu P, Xiao Z, et al. Cell Mol Life Sci. 2024 Jan 22; 81(1):50. Epub 2024 Jan 22.
Analysis of GATA3 and FOXA2 expression suggests that downregulation of genes involved in the maintenance of a mature yolk sac tumor phenotype may underlie sarcomatoid transformation. [Virchows Arch. 2024]
Analysis of GATA3 and FOXA2 expression suggests that downregulation of genes involved in the maintenance of a mature yolk sac tumor phenotype may underlie sarcomatoid transformation.
Ricci C, Ambrosi F, Grillini A, Massari F, Fiorentino M, Colecchia M, Ulbright TM, Acosta AM. Virchows Arch. 2024 Apr; 484(4):709-713. Epub 2023 Dec 23.

RefSeq alternative splicing
See 4 reference mRNA sequence splice variants for the FOXA2 gene.

Homo sapiens HNF-3beta mRNA for hepatocyte nuclear factor-3 beta, complete cds
Homo sapiens HNF-3beta mRNA for hepatocyte nuclear factor-3 beta, complete cds
gi|4958949|dbj|AB028021.1|

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Nucleotide