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Prmt3rs32892158-C
Allele Detail
Summary
Symbol: Prmt3rs32892158-C
Name: protein arginine N-methyltransferase 3; rs32892158 SNP allele with the C variant
MGI ID: MGI:7529472
Gene: Prmt3  Location: Chr7:49428094-49508013 bp, + strand  Genetic Position: Chr7, 31.44 cM
Alliance: Prmt3rs32892158-C page
Mutation
origin
Strain of Origin:  129T1/Sv
Mutation
description
Allele Type:    Not Applicable (Not Applicable)
Mutation:    Not Applicable
 
Mutation detailsThe SNP variant at this location produces a non-synonymous amino acid substitution of valine with alanine at position 273 (V273A) between LTXBJ/Sv to 129T1/Sv. (J:340388)
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 Prmt3 Mutation:  46 strains or lines available
References
Original:  J:340388 Miyazaki T, et al., Identification of Two Additional Genomic Loci Responsible for experimentally induced testicular teratoma 2 and 3 (ett2 and ett3). Zoolog Sci. 2018;35(2):172-178
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
01/28/2026
MGI 6.24
The Jackson Laboratory