RecName: Full=Lipoxygenase homology domain-containing protein 1

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Loxhd1 Mutations Cause Mechanotransduction Defects in Cochlear Hair Cells. [J Neurosci. 2021]
Loxhd1 Mutations Cause Mechanotransduction Defects in Cochlear Hair Cells.
Trouillet A, Miller KK, George SS, Wang P, Ali NE, Ricci A, Grillet N. J Neurosci. 2021 Apr 14; 41(15):3331-3343. Epub 2021 Mar 11.
Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans. [Am J Hum Genet. 2009]
Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans.
Grillet N, Schwander M, Hildebrand MS, Sczaniecka A, Kolatkar A, Velasco J, Webster JA, Kahrizi K, Najmabadi H, Kimberling WJ, et al. Am J Hum Genet. 2009 Sep; 85(3):328-37.
TMHS is an integral component of the mechanotransduction machinery of cochlear hair cells. [Cell. 2012]
TMHS is an integral component of the mechanotransduction machinery of cochlear hair cells.
Xiong W, Grillet N, Elledge HM, Wagner TF, Zhao B, Johnson KR, Kazmierczak P, Müller U. Cell. 2012 Dec 7; 151(6):1283-95.

RefSeq protein isoforms
See 2 reference sequence protein isoforms for the Loxhd1 gene.

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Mouse Genome Informatics (MGI) [Mouse Genome Informatics (MGI)]
Mouse Genome Informatics (MGI)
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reagents [ExactAntigen/Labome]
reagents
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Protein