RecName: Full=Coiled-coil domain-containing protein 39

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Biallelic Variants in CCDC39 Gene Lead to Primary Ciliary Dyskinesia and Kartagener Syndrome. [Biomed Res Int. 2022]
Biallelic Variants in CCDC39 Gene Lead to Primary Ciliary Dyskinesia and Kartagener Syndrome.
Shi X, Geng H, Yu H, Hu X, Wang G, Yang J, Zhao H. Biomed Res Int. 2022; 2022:7130555. Epub 2022 Jun 26.
A novel CCDC39 mutation causes multiple morphological abnormalities of the flagella in a primary ciliary dyskinesia patient. [Reprod Biomed Online. 2021]
A novel CCDC39 mutation causes multiple morphological abnormalities of the flagella in a primary ciliary dyskinesia patient.
Chen D, Liang Y, Li J, Zhang X, Zheng R, Wang X, Zhang H, Shen Y. Reprod Biomed Online. 2021 Nov; 43(5):920-930. Epub 2021 Jul 22.
Clinical and genetic spectrum in 33 Egyptian families with suspected primary ciliary dyskinesia. [Clin Genet. 2020]
Clinical and genetic spectrum in 33 Egyptian families with suspected primary ciliary dyskinesia.
Fassad MR, Shoman WI, Morsy H, Patel MP, Radwan N, Jenkins L, Cullup T, Fouda E, Mitchison HM, Fasseeh N. Clin Genet. 2020 Mar; 97(3):509-515. Epub 2019 Dec 5.

RefSeq genomic sequence
See the genomic reference sequence for the CCDC39 gene (NG_029581.1).
RefSeq protein
See the reference protein sequence for coiled-coil domain-containing protein 39 (NP_852091.1).

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Q9UFE4 [Domain Mapping of Disease Mut...]
Q9UFE4
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagent reviews [ExactAntigen/Labome]
reagent reviews
ExactAntigen/Labome
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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