calcium-binding protein 4 isoform X2 [Rattus norvegicus]

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Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness. [Am J Hum Genet. 2006]
Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness.
Zeitz C, Kloeckener-Gruissem B, Forster U, Kohl S, Magyar I, Wissinger B, Mátyás G, Borruat FX, Schorderet DF, Zrenner E, et al. Am J Hum Genet. 2006 Oct; 79(4):657-67. Epub 2006 Aug 23.
Characterization of C-terminal Splice Variants of Cav1.4 Ca2+ Channels in Human Retina. [J Biol Chem. 2016]
Characterization of C-terminal Splice Variants of Cav1.4 Ca2+ Channels in Human Retina.
Haeseleer F, Williams B, Lee A. J Biol Chem. 2016 Jul 22; 291(30):15663-73. Epub 2016 May 17.
A critical role of CaBP4 in the cone synapse. [Invest Ophthalmol Vis Sci. 2005]
A critical role of CaBP4 in the cone synapse.
Maeda T, Lem J, Palczewski K, Haeseleer F. Invest Ophthalmol Vis Sci. 2005 Nov; 46(11):4320-7.

RefSeq mRNA
See reference mRNA sequence for the Cabp4 gene (XM_039085454.2).
RefSeq protein isoforms
See 4 reference sequence protein isoforms for the Cabp4 gene.

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Protein