Homo sapiens KIAA0567 mRNA for KIAA0567 protein

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Characteristics of autosomal dominant WFS1-associated optic neuropathy and its comparability to OPA1-associated autosomal dominant optic atrophy. [Sci Rep. 2024]
Characteristics of autosomal dominant WFS1-associated optic neuropathy and its comparability to OPA1-associated autosomal dominant optic atrophy.
de Muijnck C, Haer-Wigman L, van Everdingen JAM, Lushchyk T, Heutinck PAT, van Dooren MF, Kievit AJA, Verhoeven VJM, Simon MEH, Wasmann RA, et al. Sci Rep. 2024 Oct 3; 14(1):22956. Epub 2024 Oct 3.
BioID-based intact cell interactome of the Kv1.3 potassium channel identifies a Kv1.3-STAT3-p53 cellular signaling pathway. [Sci Adv. 2024]
BioID-based intact cell interactome of the Kv1.3 potassium channel identifies a Kv1.3-STAT3-p53 cellular signaling pathway.
Prosdocimi E, Carpanese V, Todesca LM, Varanita T, Bachmann M, Festa M, Bonesso D, Perez-Verdaguer M, Carrer A, Velle A, et al. Sci Adv. 2024 Sep 6; 10(36):eadn9361. Epub 2024 Sep 4.
Drosophila model to clarify the pathological significance of OPA1 in autosomal dominant optic atrophy. [Elife. 2024]
Drosophila model to clarify the pathological significance of OPA1 in autosomal dominant optic atrophy.
Nitta Y, Osaka J, Maki R, Hakeda-Suzuki S, Suzuki E, Ueki S, Suzuki T, Sugie A. Elife. 2024 Aug 23; 12. Epub 2024 Aug 23.

RefSeq alternative splicing
See 34 reference mRNA sequence splice variants for the OPA1 gene.

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Nucleotide