dynein axonemal heavy chain 7 isoform X9 [Homo sapiens]

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Loss of function mutation in DNAH7 induces male infertility associated with abnormalities of the sperm flagella and mitochondria in human. [Clin Genet. 2022]
Loss of function mutation in DNAH7 induces male infertility associated with abnormalities of the sperm flagella and mitochondria in human.
Gao Y, Liu L, Shen Q, Fu F, Xu C, Geng H, Lv M, Li K, Tang D, Song B, et al. Clin Genet. 2022 Aug; 102(2):130-135. Epub 2022 May 17.
Bi-allelic mutations in DNAH7 cause asthenozoospermia by impairing the integrality of axoneme structure. [Acta Biochim Biophys Sin (Shan...]
Bi-allelic mutations in DNAH7 cause asthenozoospermia by impairing the integrality of axoneme structure.
Wei X, Sha Y, Wei Z, Zhu X, He F, Zhang X, Liu W, Wang Y, Lu Z. Acta Biochim Biophys Sin (Shanghai). 2021 Oct 12; 53(10):1300-1309.
Identification of dynein heavy chain 7 as an inner arm component of human cilia that is synthesized but not assembled in a case of primary ciliary dyskinesia. [J Biol Chem. 2002]
Identification of dynein heavy chain 7 as an inner arm component of human cilia that is synthesized but not assembled in a case of primary ciliary dyskinesia.
Zhang YJ, O'Neal WK, Randell SH, Blackburn K, Moyer MB, Boucher RC, Ostrowski LE. J Biol Chem. 2002 May 17; 277(20):17906-15. Epub 2002 Mar 4.

RefSeq mRNA
See reference mRNA sequence for the DNAH7 gene (XM_011511495.4).
RefSeq protein isoforms
See 19 reference sequence protein isoforms for the DNAH7 gene.

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Protein