n-TRtct5^rs46447118-C
Allele Detail

Summary

• Symbol: n-TRtct5^rs46447118-C
• Name: nuclear encoded tRNA arginine 5 (anticodon TCT); rs46447118 SNP allele with the C variant
• MGI ID: MGI:5779297
• Gene: n-TRtct5 Location: Chr1:173217895-173217968 bp, + strand Genetic Position: Chr1, Syntenic
• Alliance: n-TRtct5^rs46447118-C page

Mutation origin

• Strain of Origin: various

Mutation description

• Allele Type: Not Applicable
• Mutation: Undefined
• Mutation details: The C variant of SNP rs46447118 is detected in, amongst others, 129P2/OlaHsd, 129S1/SvImJ, 129S5SvEvBrd, A/J, BALB/cJ ,C57BL/6NJ, LG/J and SM/J. (J:211326)

Expression

In Mice Carrying this Mutation:

1 RNA-Seq or microarray experiment(s)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 0 strains available Cell Lines: 0 lines available
• Carrying any n-TRtct5 Mutation: 3 strains or lines available

References

• Original: J:211326 Ishimura R, et al., RNA function. Ribosome stalling induced by mutation of a CNS-specific tRNA causes neurodegeneration. Science. 2014 Jul 25;345(6195):455-9
• All: 4 reference(s)