Homo sapiens formin homology 2 domain containing 3, mRNA (cDNA clone I - Nucleotide

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A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort study. [PLoS One. 2023]
A novel splice-site FHOD3 founder variant is a common cause of hypertrophic cardiomyopathy in the population of the Balkans-A cohort study.
Vodnjov N, Toplišek J, Maver A, Čuturilo G, Jaklič H, Teran N, Višnjar T, Škrjanec Pušenjak M, Hodžić A, Miljanović O, et al. PLoS One. 2023; 18(12):e0294969. Epub 2023 Dec 5.
OpenCell: Endogenous tagging for the cartography of human cellular organization. [Science. 2022]
OpenCell: Endogenous tagging for the cartography of human cellular organization.
Cho NH, Cheveralls KC, Brunner AD, Kim K, Michaelis AC, Raghavan P, Kobayashi H, Savy L, Li JY, Canaj H, et al. Science. 2022 Mar 11; 375(6585):eabi6983. Epub 2022 Mar 11.
Linking nuclear matrix-localized PIAS1 to chromatin SUMOylation via direct binding of histones H3 and H2A.Z. [J Biol Chem. 2021]
Linking nuclear matrix-localized PIAS1 to chromatin SUMOylation via direct binding of histones H3 and H2A.Z.
Chen Z, Zhang Y, Guan Q, Zhang H, Luo J, Li J, Wei W, Xu X, Liao L, Wong J, et al. J Biol Chem. 2021 Oct; 297(4):101200. Epub 2021 Sep 17.

RefSeq alternative splicing
See 87 reference mRNA sequence splice variants for the FHOD3 gene.

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Nucleotide