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night blindness
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NYX
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness
GRM6
The whole nucleotide sequence and chromosomal localization of the gene for human metabotropic glutamate receptor subtype 6
TRPM1
Chromosomal localization and genomic characterization of the mouse melastatin gene (Mlsn1)
GPR179
Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness.
LRIT3
Whole-exome sequencing identifies LRIT3 mutations as a cause of autosomal-recessive complete congenital stationary night blindness
CACNA1F
Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F
A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants
RHO
Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa
A six-generation family with autosomal dominant retinitis pigmentosa and a rhodopsin gene mutation (arginine-135-leucine)
Recombination between rhodopsin and locus D3S47 (C17) in rhodopsin retinitis pigmentosa families
Ocular findings associated with a rhodopsin gene codon 106 mutation. Glycine-to-arginine change in autosomal dominant retinitis pigmentosa
PDE6B
Restoration of vision in the pde6����-deficient dog, a large animal model of rod-cone dystrophy
Transcriptional and post-transcriptional regulation of the rod cGMP-phosphodiesterase beta-subunit gene. Recent advances and current concepts
Chromosome mapping of the rod photoreceptor cGMP phosphodiesterase beta-subunit gene in mouse and human: tight linkage to the Huntington disease region (4p16.3)
GNAT1
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
The DNA sequence, annotation and analysis of human chromosome 3.
Cancer Gene Census
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Phototransduction
Homo sapiens (human)
4 genes
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