Homo sapiens HNF1 homeobox B, mRNA (cDNA clone MGC:21262 IMAGE:4414015 - Nucleotide

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Prenatal diagnosis and perinatal findings of 17q12 microdeletion encompassing HNF1B in a fetus with bilateral hyperechogenic kidneys on fetal ultrasound and mild renal abnormality after birth, and a review of the literature of prenatal diagnosis of 17q12 microdeletion. [Taiwan J Obstet Gynecol. 2024]
Prenatal diagnosis and perinatal findings of 17q12 microdeletion encompassing HNF1B in a fetus with bilateral hyperechogenic kidneys on fetal ultrasound and mild renal abnormality after birth, and a review of the literature of prenatal diagnosis of 17q12 microdeletion.
Chen CP, Wu FT, Pan YT, Wu PS, Wang W. Taiwan J Obstet Gynecol. 2024 Jan; 63(1):77-80.
Hepatocyte nuclear factor 1B deletion, but not intragenic mutation, might be more susceptible to hypomagnesemia. [J Diabetes Investig. 2024]
Hepatocyte nuclear factor 1B deletion, but not intragenic mutation, might be more susceptible to hypomagnesemia.
Wang Y, Xiao X, Lin Q, Song R, Wang X, Liang Y, Chen J, Luan X, Zhou Z, Xiao Y, et al. J Diabetes Investig. 2024 Jan; 15(1):121-130. Epub 2023 Sep 22.
Characterization of the prenatal renal phenotype associated with 17q12, HNF1B, microdeletions. [Prenat Diagn. 2024]
Characterization of the prenatal renal phenotype associated with 17q12, HNF1B, microdeletions.
Verscaj CP, Velez-Bartolomei F, Bodle E, Chan K, Lyons MJ, Thorson W, Tan WH, Rodig N, Graham JM Jr, Peron A, et al. Prenat Diagn. 2024 Feb; 44(2):237-246. Epub 2023 Aug 26.

RefSeq alternative splicing
See 23 reference mRNA sequence splice variants for the HNF1B gene.

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Nucleotide