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Allele : Nras<tm1.1Nesh> neuroblastoma ras oncogene; targeted mutation 1.1, Norman E Sharpless

Primary Identifier  MGI:5645358 Allele Type  Targeted
Attribute String  Conditional ready Gene  Nras
Transmission  Germline Strain of Origin  129P2/OlaHsd
Is Recombinase  false Is Wild Type  false
molecularNote  The 5' untranslated region (5'-UTR) of the gene is interrupted 1,046 base pairs downstream of the transcription start site by a splice acceptor followed by a 3XSTOP transcriptional/translational termination sequence and a single frt site (remaining after excision of a selection cassette from Nrastm1Nesh by FLP recombinase). A single point mutation in exon 2 has replaced 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.
  • mutations:
  • Single point mutation,
  • Insertion
  • synonyms:
  • LSL-N-Ras<Q61R>,
  • LSL-Nras<Q61R>,
  • LSL-N-Ras<Q61R>,
  • LSL-Nras<Q61R>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

4 Carried By

Trail: Allele

0 Driven By

14 Publication categories

Trail: Allele