PREDICTED: Homo sapiens chromosome 14 open reading frame 39 (C14orf39) - Nucleotide

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In silico analysis of a novel pathogenic variant c.7G > A in C14orf39 gene identified by WES in a Pakistani family with azoospermia. [Mol Genet Genomics. 2022]
In silico analysis of a novel pathogenic variant c.7G > A in C14orf39 gene identified by WES in a Pakistani family with azoospermia.
Ali H, Unar A, Zubair M, Dil S, Ullah F, Khan I, Hussain A, Shi Q. Mol Genet Genomics. 2022 May; 297(3):719-730. Epub 2022 Mar 19.
Variations of C14ORF39 and SYCE1 Identified in Idiopathic Premature Ovarian Insufficiency and Nonobstructive Azoospermia. [J Clin Endocrinol Metab. 2022]
Variations of C14ORF39 and SYCE1 Identified in Idiopathic Premature Ovarian Insufficiency and Nonobstructive Azoospermia.
Hou D, Yao C, Xu B, Luo W, Ke H, Li Z, Qin Y, Guo T. J Clin Endocrinol Metab. 2022 Feb 17; 107(3):724-734.
Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans. [Am J Hum Genet. 2021]
Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans.
Fan S, Jiao Y, Khan R, Jiang X, Javed AR, Ali A, Zhang H, Zhou J, Naeem M, Murtaza G, et al. Am J Hum Genet. 2021 Feb 4; 108(2):324-336. Epub 2021 Jan 27.