Incidental Mutation 'R1667:Or5j3'
ID 187259
Institutional Source Beutler Lab
Gene Symbol Or5j3
Ensembl Gene ENSMUSG00000047149
Gene Name olfactory receptor family 5 subfamily J member 3
Synonyms GA_x6K02T2Q125-47777498-47778436, Olfr1052, MOR172-1
MMRRC Submission 039703-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.131) question?
Stock # R1667 (G1)
Quality Score 225
Status Validated
Chromosome 2
Chromosomal Location 86128162-86129100 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 86129080 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Valine at position 307 (M307V)
Ref Sequence ENSEMBL: ENSMUSP00000058454 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000054746] [ENSMUST00000215090] [ENSMUST00000217166]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000054746
AA Change: M307V

PolyPhen 2 Score 0.020 (Sensitivity: 0.95; Specificity: 0.80)
SMART Domains Protein: ENSMUSP00000058454
Gene: ENSMUSG00000047149
AA Change: M307V

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 1.3e-51 PFAM
Pfam:7tm_1 41 290 6.9e-16 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000215090
AA Change: M307V

PolyPhen 2 Score 0.020 (Sensitivity: 0.95; Specificity: 0.80)
Predicted Effect probably benign
Transcript: ENSMUST00000217166
AA Change: M307V

PolyPhen 2 Score 0.020 (Sensitivity: 0.95; Specificity: 0.80)
Meta Mutation Damage Score 0.2487 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.5%
  • 20x: 93.0%
Validation Efficiency 99% (76/77)
MGI Phenotype FUNCTION: Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 73 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgra1 G A 7: 139,425,564 (GRCm39) A26T possibly damaging Het
Adgrg3 T A 8: 95,760,001 (GRCm39) Y73* probably null Het
Alk A T 17: 72,218,562 (GRCm39) V761E probably damaging Het
Ankrd13a T C 5: 114,924,794 (GRCm39) V93A possibly damaging Het
Anks1b T C 10: 90,347,046 (GRCm39) probably null Het
Arb2a T A 13: 77,907,635 (GRCm39) M1K probably null Het
Ascl1 T C 10: 87,328,655 (GRCm39) N99S probably benign Het
Atm A T 9: 53,412,232 (GRCm39) L972Q probably damaging Het
Atp2c1 A T 9: 105,309,996 (GRCm39) L566Q probably null Het
Bank1 T A 3: 135,799,057 (GRCm39) Y629F probably damaging Het
Bod1l G T 5: 41,974,118 (GRCm39) L2399I probably benign Het
Bub1b G A 2: 118,471,670 (GRCm39) G1010D probably benign Het
Ces1b G A 8: 93,783,532 (GRCm39) H563Y possibly damaging Het
Cfap70 T C 14: 20,454,225 (GRCm39) E853G probably benign Het
Cfh T C 1: 140,033,261 (GRCm39) E779G probably benign Het
Cox7c A G 13: 86,194,003 (GRCm39) S7P probably benign Het
Cyp2c67 A G 19: 39,632,034 (GRCm39) probably null Het
Dhx30 G T 9: 109,914,513 (GRCm39) L995I possibly damaging Het
Dhx30 G C 9: 109,914,514 (GRCm39) N957K possibly damaging Het
Dsc3 T C 18: 20,124,617 (GRCm39) T36A possibly damaging Het
Dstyk A G 1: 132,384,657 (GRCm39) D717G probably damaging Het
Dusp10 A G 1: 183,769,055 (GRCm39) D7G probably damaging Het
E230001N04Rik T G 17: 28,742,935 (GRCm39) noncoding transcript Het
Ece2 T C 16: 20,456,588 (GRCm39) S330P possibly damaging Het
Frmd5 ATAGTGGAATTGTTCAAACTC ATAGTGGAATTGTTCAAACTCTAGTGGAATTGTTCAAACTC 2: 121,379,211 (GRCm39) probably null Het
Gata3 T C 2: 9,882,360 (GRCm39) H14R possibly damaging Het
Ggta1 T A 2: 35,304,295 (GRCm39) I75F possibly damaging Het
Hcn1 A T 13: 117,739,609 (GRCm39) I124F unknown Het
Herpud1 A C 8: 95,115,994 (GRCm39) D53A probably damaging Het
Inhba T A 13: 16,201,209 (GRCm39) L257Q possibly damaging Het
Itga10 C T 3: 96,559,054 (GRCm39) probably benign Het
Jmy T A 13: 93,634,878 (GRCm39) S313C probably damaging Het
Lpo G A 11: 87,698,067 (GRCm39) probably benign Het
Lsg1 T C 16: 30,390,170 (GRCm39) E315G probably damaging Het
Lsm14a T A 7: 34,065,079 (GRCm39) T167S possibly damaging Het
Lsmem1 GTACATACATACATACATACATACATACA GTACATACATACATACATACATACATACATACA 12: 40,235,260 (GRCm39) probably null Het
Map3k2 T C 18: 32,336,845 (GRCm39) probably benign Het
Mapk12 A T 15: 89,024,344 (GRCm39) M81K probably damaging Het
Matn2 T A 15: 34,378,878 (GRCm39) C305S probably damaging Het
Mgam T C 6: 40,653,978 (GRCm39) Y844H possibly damaging Het
Mgat5b A G 11: 116,838,203 (GRCm39) R281G probably benign Het
Mon1b T G 8: 114,368,589 (GRCm39) C497G probably damaging Het
Mybbp1a A T 11: 72,336,043 (GRCm39) H452L probably benign Het
Mybl2 A G 2: 162,917,616 (GRCm39) T41A probably damaging Het
Ncoa5 A G 2: 164,843,623 (GRCm39) V540A probably damaging Het
Nup93 T A 8: 95,019,315 (GRCm39) V47E possibly damaging Het
Or10a4 A T 7: 106,696,977 (GRCm39) M102L probably benign Het
Orc6 T A 8: 86,031,914 (GRCm39) C100S possibly damaging Het
Otogl G T 10: 107,649,826 (GRCm39) Y1176* probably null Het
Patj A T 4: 98,301,264 (GRCm39) D183V probably damaging Het
Pik3r3 A G 4: 116,079,514 (GRCm39) T4A probably damaging Het
Pla2g4d G A 2: 120,100,631 (GRCm39) probably benign Het
Pla2r1 A G 2: 60,250,601 (GRCm39) I1407T probably benign Het
Pramel13 A T 4: 144,119,606 (GRCm39) C320* probably null Het
Prex2 A T 1: 11,256,981 (GRCm39) H1231L probably benign Het
Prkca A G 11: 107,874,772 (GRCm39) V390A probably damaging Het
Psmd13 T A 7: 140,470,522 (GRCm39) W255R probably damaging Het
Rec8 T A 14: 55,856,253 (GRCm39) N37K probably damaging Het
Rnf207 C T 4: 152,397,672 (GRCm39) E361K probably benign Het
Serpina3f T A 12: 104,183,699 (GRCm39) L187Q probably damaging Het
Skint11 A T 4: 114,051,978 (GRCm39) T109S probably damaging Het
Slc7a8 A G 14: 54,962,306 (GRCm39) S443P probably damaging Het
Slc8b1 T A 5: 120,659,147 (GRCm39) F197Y probably benign Het
Sox2 T C 3: 34,704,568 (GRCm39) Y2H probably damaging Het
Speg T A 1: 75,387,193 (GRCm39) probably benign Het
Tlr3 T C 8: 45,853,874 (GRCm39) N149D probably benign Het
Trim60 A C 8: 65,454,116 (GRCm39) D44E probably benign Het
Ugt1a7c A G 1: 88,023,657 (GRCm39) Y272C probably damaging Het
Vmn1r4 T A 6: 56,933,738 (GRCm39) Y81N probably damaging Het
Vmn2r73 A T 7: 85,506,889 (GRCm39) C808S probably benign Het
Ythdf3 T C 3: 16,259,056 (GRCm39) I412T possibly damaging Het
Zfp672 T C 11: 58,206,921 (GRCm39) T467A possibly damaging Het
Zfp985 A T 4: 147,668,407 (GRCm39) Q425L possibly damaging Het
Other mutations in Or5j3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02632:Or5j3 APN 2 86,128,904 (GRCm39) missense probably damaging 0.99
IGL02988:Or5j3 UTSW 2 86,128,823 (GRCm39) missense probably damaging 0.99
R0382:Or5j3 UTSW 2 86,128,937 (GRCm39) missense probably damaging 1.00
R0569:Or5j3 UTSW 2 86,128,941 (GRCm39) missense probably damaging 1.00
R1476:Or5j3 UTSW 2 86,128,823 (GRCm39) missense probably damaging 0.99
R1510:Or5j3 UTSW 2 86,128,715 (GRCm39) missense probably damaging 1.00
R2912:Or5j3 UTSW 2 86,128,733 (GRCm39) missense probably damaging 0.96
R2913:Or5j3 UTSW 2 86,128,733 (GRCm39) missense probably damaging 0.96
R3937:Or5j3 UTSW 2 86,128,360 (GRCm39) missense probably damaging 1.00
R4299:Or5j3 UTSW 2 86,128,585 (GRCm39) missense possibly damaging 0.46
R4774:Or5j3 UTSW 2 86,129,042 (GRCm39) missense possibly damaging 0.91
R5027:Or5j3 UTSW 2 86,128,540 (GRCm39) missense possibly damaging 0.84
R5080:Or5j3 UTSW 2 86,128,258 (GRCm39) missense probably benign 0.22
R5254:Or5j3 UTSW 2 86,128,265 (GRCm39) missense probably damaging 1.00
R5389:Or5j3 UTSW 2 86,128,561 (GRCm39) missense possibly damaging 0.90
R6110:Or5j3 UTSW 2 86,129,019 (GRCm39) missense probably damaging 0.99
R6492:Or5j3 UTSW 2 86,128,990 (GRCm39) missense probably benign 0.05
R6810:Or5j3 UTSW 2 86,128,267 (GRCm39) missense probably benign 0.01
R7095:Or5j3 UTSW 2 86,129,021 (GRCm39) missense probably benign 0.08
R7104:Or5j3 UTSW 2 86,128,564 (GRCm39) missense probably benign
R7320:Or5j3 UTSW 2 86,128,338 (GRCm39) frame shift probably null
R7328:Or5j3 UTSW 2 86,128,338 (GRCm39) frame shift probably null
R7363:Or5j3 UTSW 2 86,128,338 (GRCm39) frame shift probably null
R8048:Or5j3 UTSW 2 86,128,672 (GRCm39) missense probably benign 0.04
R8202:Or5j3 UTSW 2 86,128,968 (GRCm39) missense probably benign 0.06
R8968:Or5j3 UTSW 2 86,128,526 (GRCm39) missense probably benign 0.00
R9160:Or5j3 UTSW 2 86,128,330 (GRCm39) missense probably benign 0.40
R9321:Or5j3 UTSW 2 86,128,297 (GRCm39) missense probably benign 0.01
R9694:Or5j3 UTSW 2 86,128,718 (GRCm39) missense probably benign 0.03
Z1176:Or5j3 UTSW 2 86,128,570 (GRCm39) missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- GCTTTAATTACATTCAGCCAAGCTCCCA -3'
(R):5'- TGACTGTAACTACACTGTCAGAGGAAGG -3'

Sequencing Primer
(F):5'- AGCCAAGCTCCCAGTATTCTG -3'
(R):5'- TCTCCAAAAGACATAATGTTCTCTTG -3'
Posted On 2014-05-09