Incidental Mutation 'R7328:Or5j3'
ID 569034
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 045421-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.138) question?
Stock # R7328 (G1)
Quality Score 217.468
Status Not validated
Chromosome 2
Chromosomal Location 86128162-86129100 bp(+) (GRCm39)
Type of Mutation frame shift
DNA Base Change (assembly) GTACTTTTT to GT at 86128338 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000149344 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000054746] [ENSMUST00000215090] [ENSMUST00000217166]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000054746
SMART Domains Protein: ENSMUSP00000058454
Gene: ENSMUSG00000047149

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 1.3e-51 PFAM
Pfam:7tm_1 41 290 6.9e-16 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000215090
Predicted Effect probably null
Transcript: ENSMUST00000217166
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency
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: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933427D14Rik C G 11: 72,060,606 (GRCm39) probably null Het
Abca13 T A 11: 9,241,545 (GRCm39) V1136E probably benign Het
Arl4c C A 1: 88,629,239 (GRCm39) E50* probably null Het
Atxn7l1 T C 12: 33,198,502 (GRCm39) probably null Het
Ctdsp1 A T 1: 74,433,199 (GRCm39) I115F probably damaging Het
Cyp2j5 A G 4: 96,551,450 (GRCm39) V91A probably damaging Het
Dscam T A 16: 96,446,235 (GRCm39) K1469* probably null Het
Elf2 A G 3: 51,174,198 (GRCm39) C110R probably damaging Het
Ephb1 A G 9: 102,072,438 (GRCm39) Y114H probably damaging Het
Ephb2 C T 4: 136,386,245 (GRCm39) probably null Het
Fbxw20 C A 9: 109,061,383 (GRCm39) C122F probably damaging Het
Flnb T C 14: 7,883,788 (GRCm38) I338T possibly damaging Het
Flnb T A 14: 7,894,660 (GRCm38) Y819* probably null Het
Foxo3 A T 10: 42,073,258 (GRCm39) S420T probably benign Het
Herpud1 T C 8: 95,113,248 (GRCm39) V10A possibly damaging Het
Hmcn1 A T 1: 150,514,617 (GRCm39) V3585E possibly damaging Het
Hsdl1 T C 8: 120,292,830 (GRCm39) T202A probably benign Het
Htr1d G A 4: 136,170,614 (GRCm39) S281N probably benign Het
Igkv14-111 T A 6: 68,233,709 (GRCm39) I70N probably damaging Het
Igkv8-34 A G 6: 70,021,328 (GRCm39) S45P probably damaging Het
Inha T C 1: 75,486,760 (GRCm39) Y352H probably damaging Het
Lats1 A T 10: 7,581,311 (GRCm39) M699L possibly damaging Het
Marchf9 T C 10: 126,894,165 (GRCm39) E146G probably damaging Het
Mcm8 T C 2: 132,674,777 (GRCm39) V443A probably benign Het
Melk A T 4: 44,332,931 (GRCm39) S296C probably benign Het
Myo18a T C 11: 77,698,737 (GRCm39) S4P Het
Myof T C 19: 37,904,847 (GRCm39) Y1646C probably damaging Het
Noc4l C A 5: 110,796,789 (GRCm39) A498S possibly damaging Het
Nrxn3 T C 12: 88,762,345 (GRCm39) S131P probably benign Het
Or5ae2 T C 7: 84,506,507 (GRCm39) I312T probably benign Het
Or5ak23 A G 2: 85,244,668 (GRCm39) I185T probably benign Het
Or8g23 T C 9: 38,971,857 (GRCm39) Y35C probably damaging Het
Pcp4l1 G A 1: 171,002,034 (GRCm39) A42V possibly damaging Het
Phldb2 T A 16: 45,578,572 (GRCm39) probably null Het
Polr2b C T 5: 77,463,846 (GRCm39) P81L probably damaging Het
Rbfa C A 18: 80,236,454 (GRCm39) G215C probably benign Het
Rdh19 T C 10: 127,692,896 (GRCm39) S188P probably damaging Het
Scn9a T C 2: 66,314,931 (GRCm39) M1596V probably benign Het
Sele A T 1: 163,876,844 (GRCm39) Y40F probably benign Het
Setd1b T A 5: 123,290,442 (GRCm39) V803D unknown Het
Siglecf C T 7: 43,001,691 (GRCm39) T167I possibly damaging Het
Slc39a6 T C 18: 24,733,987 (GRCm39) E234G probably benign Het
Slco1a1 T A 6: 141,882,134 (GRCm39) D145V possibly damaging Het
Son G A 16: 91,455,278 (GRCm39) V1342I probably benign Het
Sybu G A 15: 44,651,190 (GRCm39) P38L not run Het
Taf15 C T 11: 83,375,658 (GRCm39) T41M possibly damaging Het
Tm4sf4 A T 3: 57,333,925 (GRCm39) N71Y probably benign Het
Tm7sf2 C T 19: 6,114,156 (GRCm39) V226I possibly damaging Het
Trim66 C A 7: 109,056,958 (GRCm39) Q1066H probably damaging Het
Tyw1 T C 5: 130,291,685 (GRCm39) V51A probably benign Het
Vav3 A T 3: 109,410,744 (GRCm39) I192L probably benign 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
R1667:Or5j3 UTSW 2 86,129,080 (GRCm39) missense probably null 0.02
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
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'- CCTCCTCAGGTTTGAAAGAAGGG -3'
(R):5'- CTGCCACATAACGGTCATAAGC -3'

Sequencing Primer
(F):5'- GGAATGGCTACTGAGAACTGTAC -3'
(R):5'- GGTCATAAGCCATCACTGACAG -3'
Posted On 2019-09-13