Slc6a4^rs29413009-A
Spontaneous Allele Detail

Summary

• Symbol: Slc6a4^rs29413009-A
• Name: solute carrier family 6 (neurotransmitter transporter, serotonin), member 4; rs29413009 SNP allele with the A variant
• MGI ID: MGI:8385494
• Gene: Slc6a4 Location: Chr11:76889429-76923166 bp, + strand Genetic Position: Chr11, 46.18 cM
• Alliance: Slc6a4^rs29413009-A page

Mutation origin

• Strain of Origin: C57BL/6J

Mutation description

• Allele Type: Spontaneous (Not Applicable)
• Mutation: Single point mutation
• Mutation details:

  This A variant of the SNP is the minor variant found in the C57BL/6NJ and C57BL/6J strains. It encodes lysine 152 (AAG, p.K152) and co-occurs with the p.G39 encoding rs13481111-G minor variant (Slc6a4^rs13481111-G) in C57BL/6NJ and C57BL/6J. (J:144958)

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 Slc6a4 Mutation: 59 strains or lines available

References

• Original: J:144958 Carneiro AM, et al., Functional coding variation in recombinant inbred mouse lines reveals multiple serotonin transporter-associated phenotypes. Proc Natl Acad Sci U S A. 2009 Feb 10;106(6):2047-52
• All: 1 reference(s)