Homo sapiens deafness, autosomal recessive 59, mRNA (cDNA clone MGC:15 - Nucleotide

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Novel Pathogenic Variants in PJVK, the Gene Encoding Pejvakin, in Subjects with Autosomal Recessive Non-Syndromic Hearing Impairment and Auditory Neuropathy Spectrum Disorder. [Genes (Basel). 2022]
Novel Pathogenic Variants in PJVK, the Gene Encoding Pejvakin, in Subjects with Autosomal Recessive Non-Syndromic Hearing Impairment and Auditory Neuropathy Spectrum Disorder.
Domínguez-Ruiz M, Rodríguez-Ballesteros M, Gandía M, Gómez-Rosas E, Villamar M, Scimemi P, Mancini P, Rendtorff ND, Moreno-Pelayo MA, Tranebjaerg L, et al. Genes (Basel). 2022 Jan 15; 13(1). Epub 2022 Jan 15.
Inflammation-dependent overexpression of c-Myc enhances CRL4(DCAF4) E3 ligase activity and promotes ubiquitination of ST7 in colitis-associated cancer. [J Pathol. 2019]
Inflammation-dependent overexpression of c-Myc enhances CRL4(DCAF4) E3 ligase activity and promotes ubiquitination of ST7 in colitis-associated cancer.
Liu H, Lu W, He H, Wu J, Zhang C, Gong H, Yang C. J Pathol. 2019 Aug; 248(4):464-475. Epub 2019 Apr 22.
Targeted Mutation Analysis of the SLC26A4, MYO6, PJVK and CDH23 Genes in Iranian Patients with AR Nonsyndromic Hearing Loss. [Fetal Pediatr Pathol. 2019]
Targeted Mutation Analysis of the SLC26A4, MYO6, PJVK and CDH23 Genes in Iranian Patients with AR Nonsyndromic Hearing Loss.
Alimardani M, Hosseini SM, Khaniani MS, Haghi MR, Eslahi A, Farjami M, Chezgi J, Derakhshan SM, Mojarrad M. Fetal Pediatr Pathol. 2019 Apr; 38(2):93-102. Epub 2018 Dec 23.

RefSeq alternative splicing
See 8 reference mRNA sequence splice variants for the PJVK gene.

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Order DFNB59 cDNA clone/Protein/Antibody/RNAi [OriGene]
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Nucleotide