protein C19orf12 homolog isoform X2 [Rattus norvegicus]

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Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca²⁺. [Front Genet. 2015]
Mutations of C19orf12, coding for a transmembrane glycine zipper containing mitochondrial protein, cause mis-localization of the protein, inability to respond to oxidative stress and increased mitochondrial Ca²⁺.
Venco P, Bonora M, Giorgi C, Papaleo E, Iuso A, Prokisch H, Pinton P, Tiranti V. Front Genet. 2015; 6:185. Epub 2015 May 19.
Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12. [Hum Mutat. 2013]
Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12.
Landouré G, Zhu PP, Lourenço CM, Johnson JO, Toro C, Bricceno KV, Rinaldi C, Meilleur KG, Sangaré M, Diallo O, et al. Hum Mutat. 2013 Oct; 34(10):1357-60. Epub 2013 Aug 12.

RefSeq mRNA
See reference mRNA sequence for the C1h19orf12 gene (XM_006228917.5).
RefSeq protein isoforms
See 5 reference sequence protein isoforms for the C1h19orf12 gene.

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Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System

protein C19orf12 homolog isoform X2 [Rattus norvegicus]
protein C19orf12 homolog isoform X2 [Rattus norvegicus]
gi|564327747|ref|XP_006228979.1|

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