zinc finger protein 142 isoform X2 [Homo sapiens]

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A deleterious frameshift insertion mutation in the ZNF142 gene leads to intellectual developmental disorder with impaired speech in three affected siblings: Clinical features and literature review. [Mol Genet Genomic Med. 2023]
A deleterious frameshift insertion mutation in the ZNF142 gene leads to intellectual developmental disorder with impaired speech in three affected siblings: Clinical features and literature review.
Mir A, Song Y, Lee H, Montazer-Zohouri M, Reisi M, Tabatabaiefar MA. Mol Genet Genomic Med. 2023 Dec; 11(12):e2261. Epub 2023 Jul 26.
ZNF142 mutation causes neurodevelopmental disorder with speech impairment and seizures: Novel variants and literature review. [Eur J Med Genet. 2022]
ZNF142 mutation causes neurodevelopmental disorder with speech impairment and seizures: Novel variants and literature review.
Kamal N, Khamirani HJ, Mohammadi S, Dastgheib SA, Dianatpour M, Tabei SMB. Eur J Med Genet. 2022 Jul; 65(7):104522. Epub 2022 May 23.
Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder. [Clin Genet. 2022]
Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder.
Christensen MB, Levy AM, Mohammadi NA, Niceta M, Kaiyrzhanov R, Dentici ML, Al Alam C, Alesi V, Benoit V, Bhatia KP, et al. Clin Genet. 2022 Aug; 102(2):98-109. Epub 2022 Jun 8.

RefSeq mRNA
See reference mRNA sequence for the ZNF142 gene (XM_047445781.1).
RefSeq protein isoforms
See 34 reference sequence protein isoforms for the ZNF142 gene.

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Protein