leucine-rich repeat, immunoglobulin-like domain and transmembrane doma - Protein

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Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness. [Am J Hum Genet. 2013]
Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness.
Zeitz C, Jacobson SG, Hamel CP, Bujakowska K, Neuillé M, Orhan E, Zanlonghi X, Lancelot ME, Michiels C, Schwartz SB, et al. Am J Hum Genet. 2013 Jan 10; 92(1):67-75. Epub 2012 Dec 13.
LRIT3 Differentially Affects Connectivity and Synaptic Transmission of Cones to ON- and OFF-Bipolar Cells. [Invest Ophthalmol Vis Sci. 2017]
LRIT3 Differentially Affects Connectivity and Synaptic Transmission of Cones to ON- and OFF-Bipolar Cells.
Neuillé M, Cao Y, Caplette R, Guerrero-Given D, Thomas C, Kamasawa N, Sahel JA, Hamel CP, Audo I, Picaud S, et al. Invest Ophthalmol Vis Sci. 2017 Mar 1; 58(3):1768-1778.
Lrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB). [PLoS One. 2014]
Lrit3 deficient mouse (nob6): a novel model of complete congenital stationary night blindness (cCSNB).
Neuillé M, El Shamieh S, Orhan E, Michiels C, Antonio A, Lancelot ME, Condroyer C, Bujakowska K, Poch O, Sahel JA, et al. PLoS One. 2014; 9(3):e90342. Epub 2014 Mar 5.

RefSeq genomic sequence
See the genomic reference sequence for the LRIT3 gene (NG_033249.1).
RefSeq mRNA
See reference mRNA sequence for the LRIT3 gene (NM_198506.5).
RefSeq protein isoforms
See 5 reference sequence protein isoforms for the LRIT3 gene.

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GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
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OncoMX cancer biomarker resource
Transcript/Protein Information [PANTHER Classification System]
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reagents [ExactAntigen/Labome]
reagents
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Protein