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Article

Identification of a new mutant allele, Grm6(nob7), for complete congenital stationary night blindness.

Visual neuroscience - 1 Jan 2015

Qian Haohua, Ji Rui, Gregg Ronald G, Peachey Neal S

Abstract excerpt

Electroretinogram (ERG) studies identified a new mouse line with a normal a-wave but lacking the b-wave component. The ERG phenotype of this new allele, nob7, matched closely that of mouse mutants for Grm6, Lrit3, Trpm1, and Nyx, which encode for proteins expressed in depolarizing bipolar cells (DBCs). To identify the underlying mutation, we first crossed nob7 mice with Grm6 nob3 mutants and measured the ERGs in...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Open in PubMed Open full text

Identifiers

PMID: 26241901
DOI: 10.1017/S0952523815000012
PMCID: PMC4648616

Genes

ERG
GRM6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Identification of a new mutant allele, Grm6(nob7), for complete congenital stationary night blindness.PMID 26241901Read ↗

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