thioredoxin-like protein 4A [Macaca mulatta]

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Expanding the genotypic spectrum of TXNL4A variants in Burn-McKeown syndrome. [Clin Genet. 2022]
Expanding the genotypic spectrum of TXNL4A variants in Burn-McKeown syndrome.
Wood KA, Ellingford JM, Thomas HB, Genomics UK Research Consortium, Douzgou S, Beaman GM, Hobson E, Prescott K, O'Keefe RT, Newman WG. Clin Genet. 2022 Feb; 101(2):255-259. Epub 2021 Nov 5.
Burn-McKeown syndrome with biallelic promoter type 2 deletion in TXNL4A in two siblings. [Am J Med Genet A. 2020]
Burn-McKeown syndrome with biallelic promoter type 2 deletion in TXNL4A in two siblings.
Narayanan DL, Purushothama G, Bhavani GS, Shukla A. Am J Med Genet A. 2020 Jun; 182(6):1313-1315. Epub 2020 Mar 18.
TXNL4A-Related Craniofacial Disorders. [GeneReviews(®). 1993]
TXNL4A-Related Craniofacial Disorders.
Lüdecke HJ, Wieczorek D. GeneReviews(®). 1993-2024. 2016 Jul 14 [updated 2022 May 12]

RefSeq mRNA
See reference mRNA sequence for the TXNL4A gene (NM_001260866.1).
RefSeq protein isoforms
See the other reference sequence protein isoform for the TXNL4A gene (XP_014977710.1).

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