A splice acceptor sequence, a 3XSTOP transcriptional/translational termination sequence and a frt site-flanked neomycin resistance cassette (neor), the entire sequence flanked by loxP sites, was inserted into the 5' untranslated region (5'-UTR) 1,046 base pairs downstream of the transcription start site. A single point mutation was introduced into exon 2 that replaces a nucleotide triplet encoding glutamine at amino acid position 61 with an arginine codon (Q61R); this represents the predominant NRAS mutation observed in human melanomas. (J:220627)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
129P2/OlaHsd
Targeted
Insertion, Single point
--
1
21
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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