zinc finger protein 142 isoform X2 [Homo sapiens]

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View conserved domains detected in this protein sequence using CD-search.
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Opens the Genome Data Viewer, NCBI's genome browser, at the genomic location at which this sequence is annotated. View this sequence in the context of other features annotated at the same location and browse to other genome regions.

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 genomic sequence
See the genomic reference sequence for the ZNF142 gene (NG_033099.2).
RefSeq mRNA
See reference mRNA sequence for the ZNF142 gene (XM_054343806.1).
RefSeq protein isoforms
See 34 reference sequence protein isoforms for the ZNF142 gene.