Homo sapiens chromosome 7 open reading frame 63, mRNA (cDNA clone IMAG - Nucleotide

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A novel variant in CFAP69 causes asthenoteratozoospermia with treatable ART outcomes and a literature review. [J Assist Reprod Genet. 2023]
A novel variant in CFAP69 causes asthenoteratozoospermia with treatable ART outcomes and a literature review.
Tang X, Ma J, Wang X, Long S, Wan L, Yu H, Yang J, Huang G, Lin T. J Assist Reprod Genet. 2023 Sep; 40(9):2175-2184. Epub 2023 Jul 1.
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.
Novel homozygous CFAP69 mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagella. [J Med Genet. 2019]
Novel homozygous CFAP69 mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagella.
He X, Li W, Wu H, Lv M, Liu W, Liu C, Zhu F, Li C, Fang Y, Yang C, et al. J Med Genet. 2019 Feb; 56(2):96-103. Epub 2018 Nov 10.

RefSeq alternative splicing
See 53 reference mRNA sequence splice variants for the CFAP69 gene.

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Nucleotide