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Allele : Cnga3<cpfl5> cyclic nucleotide gated channel alpha 3; cone photoreceptor function loss 5
Primary Identifier  MGI:3608770 Allele Type  Spontaneous
Gene  Cnga3 Strain of Origin  Not Specified
Is Recombinase  false Is Wild Type  false
molecularNote  Sequence analysis of this spontaneous phenotypic mutation identified a single A to G substitution at Chr1: 37,258,096 (GRCm38.p6, sequence ATGCTGGTTCGAGCCCGG(A-to-G)CA) which changes codon ACA to GCA in exon 5, changing amino acid 165 from threonine to alanine (p.T165A).
  • mutations:
  • Single point mutation
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

1 Carried By

0 Driven By

11 Publication categories





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