RecName: Full=Metabotropic glutamate receptor 6; Short=mGluR6; Flags: - Protein

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Pseudodominant inheritance of autosomal recessive congenital stationary night blindness in one family with three co-segregating deleterious GRM6 variants identified by next-generation sequencing. [Mol Genet Genomic Med. 2019]
Pseudodominant inheritance of autosomal recessive congenital stationary night blindness in one family with three co-segregating deleterious GRM6 variants identified by next-generation sequencing.
Liu HY, Huang J, Xiao H, Zhang MJ, Shi FF, Jiang YH, Du H, He Q, Wang ZY. Mol Genet Genomic Med. 2019 Dec; 7(12):e952. Epub 2019 Nov 2.
Identification of a novel GRM6 mutation in a previously described consanguineous family with complete congenital stationary night blindness. [Ophthalmic Genet. 2019]
Identification of a novel GRM6 mutation in a previously described consanguineous family with complete congenital stationary night blindness.
Tourville A, Michiels C, Condroyer C, Meunier A, Cordonnier M, Sahel JA, Audo I, Abramowicz M, Zeitz C. Ophthalmic Genet. 2019 Apr; 40(2):182-184.
Meclofenamic acid improves the signal to noise ratio for visual responses produced by ectopic expression of human rod opsin. [Mol Vis. 2017]
Meclofenamic acid improves the signal to noise ratio for visual responses produced by ectopic expression of human rod opsin.
Eleftheriou CG, Cehajic-Kapetanovic J, Martial FP, Milosavljevic N, Bedford RA, Lucas RJ. Mol Vis. 2017; 23:334-345. Epub 2017 Jun 16.

RefSeq genomic sequence
See the genomic reference sequence for the GRM6 gene (NG_008105.1).
RefSeq protein
See the reference protein sequence for metabotropic glutamate receptor 6 precursor (NP_000834.2).

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O15303 [Domain Mapping of Disease Mut...]
O15303
Domain Mapping of Disease Mutations
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Protein