Homo sapiens chromosome 21 open reading frame 56, mRNA (cDNA clone MGC - Nucleotide

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Balanced chromosomal rearrangements implicate YIPF5 and SPATC1L in non-obstructive oligoasthenozoospermia and oligozoospermia and of a derivative chromosome 22 in recurrent miscarriage. [Gene. 2023]
Balanced chromosomal rearrangements implicate YIPF5 and SPATC1L in non-obstructive oligoasthenozoospermia and oligozoospermia and of a derivative chromosome 22 in recurrent miscarriage.
David D, Fino J, Oliveira R, Dória S, Morton CC. Gene. 2023 Dec 15; 887:147737. Epub 2023 Aug 23.
Chr21 protein-protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer's disease. [Life Sci Alliance. 2022]
Chr21 protein-protein interactions: enrichment in proteins involved in intellectual disability, autism, and late-onset Alzheimer's disease.
Viard J, Loe-Mie Y, Daudin R, Khelfaoui M, Plancon C, Boland A, Tejedor F, Huganir RL, Kim E, Kinoshita M, et al. Life Sci Alliance. 2022 Aug 1; 5(12). Epub 2022 Aug 1.
Biallelic mutations in spermatogenesis and centriole-associated 1 like (SPATC1L) cause acephalic spermatozoa syndrome and male infertility. [Asian J Androl. 2022]
Biallelic mutations in spermatogenesis and centriole-associated 1 like (SPATC1L) cause acephalic spermatozoa syndrome and male infertility.
Li YZ, Li N, Liu WS, Sha YW, Wu RF, Tang YL, Zhu XS, Wei XL, Zhang XY, Wang YF, et al. Asian J Androl. 2022 Jan-Feb; 24(1):67-72.

RefSeq alternative splicing
See 8 reference mRNA sequence splice variants for the SPATC1L gene.

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Nucleotide