TALEN-targeted homologous recombination using a synthetic oligodeoxynucleotide created a nucleotide substitution (G to T) that results in the amino acid substitution of valine for glycine at position 19 (G19V) and thereby created an additional SexAI restriction site. An identifying neutral nucleotide replacement in codon 19 (T to A) was used as a unique sequence identifier. Silent exchanges within the TALEN binding region removed an endogenous ApaLI restriction site. The G19V mutation replicated the amino acid substitution observed in Rab38cht. This allele was identified in a line established from founder mouse Rc6-4. (J:205086)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
(FVB/NCrl x C57BL/6NCrl)F1
Endonuclease-mediated
Nucleotide substitutions
--
1
--
1

Phenotypes

Legend:
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes:
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Phenotypes

References Literature

Title
PMID
Journal
Year
IF
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