PREDICTED: Homo sapiens chromosome 10 open reading frame 71 (C10orf71) - Nucleotide

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Autosomal recessive congenital cataract is associated with a novel 4-bp splicing deletion mutation in a novel C10orf71 human gene. [Hum Genomics. 2023]
Autosomal recessive congenital cataract is associated with a novel 4-bp splicing deletion mutation in a novel C10orf71 human gene.
Chograni M, Alahdal HM, Rejili M. Hum Genomics. 2023 May 13; 17(1):41. Epub 2023 May 13.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome. [Cell. 2021]
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Huttlin EL, Bruckner RJ, Navarrete-Perea J, Cannon JR, Baltier K, Gebreab F, Gygi MP, Thornock A, Zarraga G, Tam S, et al. Cell. 2021 May 27; 184(11):3022-3040.e28. Epub 2021 May 6.
Systematic bromodomain protein screens identify homologous recombination and R-loop suppression pathways involved in genome integrity. [Genes Dev. 2019]
Systematic bromodomain protein screens identify homologous recombination and R-loop suppression pathways involved in genome integrity.
Kim JJ, Lee SY, Gong F, Battenhouse AM, Boutz DR, Bashyal A, Refvik ST, Chiang CM, Xhemalce B, Paull TT, et al. Genes Dev. 2019 Dec 1; 33(23-24):1751-1774. Epub 2019 Nov 21.

RefSeq alternative splicing
See 11 reference mRNA sequence splice variants for the C10orf71 gene.
RefSeq protein product
See the reference protein sequence for cardiac-enriched FHL2-interacting protein isoform X2 (XP_047280505.1).

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Nucleotide