dynein cytoplasmic 1 heavy chain 1, isoform CRA_b [Mus musculus]

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Effect of conditional deletion of cytoplasmic dynein heavy chain DYNC1H1 on postnatal photoreceptors. [PLoS One. 2021]
Effect of conditional deletion of cytoplasmic dynein heavy chain DYNC1H1 on postnatal photoreceptors.
Dahl TM, Reed M, Gerstner CD, Ying G, Baehr W. PLoS One. 2021; 16(3):e0248354. Epub 2021 Mar 11.
Mice with an autosomal dominant Charcot-Marie-Tooth type 2O disease mutation in both dynein alleles display severe moto-sensory phenotypes. [Sci Rep. 2019]
Mice with an autosomal dominant Charcot-Marie-Tooth type 2O disease mutation in both dynein alleles display severe moto-sensory phenotypes.
Nandini S, Conley Calderon JL, Sabblah TT, Love R, King LE, King SJ. Sci Rep. 2019 Aug 19; 9(1):11979. Epub 2019 Aug 19.
A novel mouse model carrying a human cytoplasmic dynein mutation shows motor behavior deficits consistent with Charcot-Marie-Tooth type 2O disease. [Sci Rep. 2018]
A novel mouse model carrying a human cytoplasmic dynein mutation shows motor behavior deficits consistent with Charcot-Marie-Tooth type 2O disease.
Sabblah TT, Nandini S, Ledray AP, Pasos J, Calderon JLC, Love R, King LE, King SJ. Sci Rep. 2018 Jan 29; 8(1):1739. Epub 2018 Jan 29.

RefSeq protein
See the reference protein sequence for cytoplasmic dynein 1 heavy chain 1 (NP_084514.2).

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