Incidental Mutation 'R8165:Or1j11'
ID 633698
Institutional Source Beutler Lab
Gene Symbol Or1j11
Ensembl Gene ENSMUSG00000094464
Gene Name olfactory receptor family 1 subfamily E member 1
Synonyms GA_x6K02T2NLDC-33116096-33117025, MOR136-3, Olfr339
MMRRC Submission 067591-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.102) question?
Stock # R8165 (G1)
Quality Score 225.009
Status Validated
Chromosome 2
Chromosomal Location 36311412-36312341 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 36311715 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Asparagine at position 102 (Y102N)
Ref Sequence ENSEMBL: ENSMUSP00000071383 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071437]
AlphaFold Q8VGK8
Predicted Effect probably damaging
Transcript: ENSMUST00000071437
AA Change: Y102N

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000071383
Gene: ENSMUSG00000094464
AA Change: Y102N

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 3.9e-55 PFAM
Pfam:7tm_1 41 290 5e-24 PFAM
Meta Mutation Damage Score 0.3605 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.7%
Validation Efficiency 100% (65/65)
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: 62 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
0610040J01Rik C A 5: 64,055,289 (GRCm39) probably null Het
Amph A G 13: 19,279,007 (GRCm39) K161E probably benign Het
Aox1 A T 1: 58,348,088 (GRCm39) H602L probably benign Het
Areg A G 5: 91,291,492 (GRCm39) N145S probably damaging Het
Arhgap29 C T 3: 121,782,222 (GRCm39) T142I probably damaging Het
Bcar3 C T 3: 122,304,805 (GRCm39) probably benign Het
Brpf3 C T 17: 29,025,248 (GRCm39) A107V probably benign Het
Btnl2 T A 17: 34,587,682 (GRCm39) S509T possibly damaging Het
Cacna2d2 A G 9: 107,402,653 (GRCm39) probably null Het
Casz1 C T 4: 149,028,888 (GRCm39) P1111L probably damaging Het
Ccdc91 C T 6: 147,533,086 (GRCm39) T411I unknown Het
Chd9 A C 8: 91,767,769 (GRCm39) E2422A probably damaging Het
Clrn3 T C 7: 135,130,133 (GRCm39) I34V probably benign Het
Cnksr3 C T 10: 7,104,467 (GRCm39) D79N probably damaging Het
Cops8 A G 1: 90,539,729 (GRCm39) probably null Het
Cpa2 A G 6: 30,564,345 (GRCm39) K392R probably benign Het
Dnajc28 G A 16: 91,413,795 (GRCm39) R150* probably null Het
Dnase1l3 T C 14: 7,994,299 (GRCm38) probably benign Het
Gdpd5 A T 7: 99,105,689 (GRCm39) T502S probably benign Het
Gp2 A T 7: 119,049,375 (GRCm39) D387E probably damaging Het
Gpr179 A G 11: 97,242,364 (GRCm39) L160P probably benign Het
Hmcn1 G A 1: 150,522,409 (GRCm39) T3497M probably benign Het
Idh3b T A 2: 130,122,420 (GRCm39) T322S possibly damaging Het
Kit A T 5: 75,781,540 (GRCm39) N323I possibly damaging Het
Kng2 T C 16: 22,806,246 (GRCm39) S445G unknown Het
Lin54 A G 5: 100,602,358 (GRCm39) V393A probably benign Het
Lyst T A 13: 13,872,945 (GRCm39) W2715R probably damaging Het
Mad1l1 T C 5: 140,300,813 (GRCm39) T28A probably benign Het
Med7 T A 11: 46,332,073 (GRCm39) C223S probably benign Het
Megf8 T A 7: 25,053,298 (GRCm39) L1823Q probably damaging Het
Mga C A 2: 119,777,719 (GRCm39) Q1755K probably benign Het
Mgat4b A T 11: 50,101,801 (GRCm39) N22I probably benign Het
Ndufb6 C T 4: 40,270,665 (GRCm39) probably null Het
Neil3 A G 8: 54,042,129 (GRCm39) L490P probably benign Het
Nek9 C T 12: 85,350,417 (GRCm39) V886I probably benign Het
Nol4l A T 2: 153,262,473 (GRCm39) Y366* probably null Het
Nt5dc2 A G 14: 30,860,886 (GRCm39) T354A probably damaging Het
Pde2a G A 7: 101,149,655 (GRCm39) probably null Het
Phf1 T C 17: 27,156,044 (GRCm39) F444L possibly damaging Het
Plin4 G A 17: 56,414,019 (GRCm39) T202I possibly damaging Het
Plk4 G C 3: 40,768,009 (GRCm39) V851L probably damaging Het
Pp2d1 A G 17: 53,822,257 (GRCm39) S270P probably damaging Het
Ripor1 C A 8: 106,347,520 (GRCm39) L1028M unknown Het
Scn9a A G 2: 66,370,874 (GRCm39) F569L probably damaging Het
Sel1l2 T A 2: 140,104,626 (GRCm39) L306F probably damaging Het
Spic A T 10: 88,513,428 (GRCm39) S86T probably damaging Het
Spmip10 T A 18: 56,722,547 (GRCm39) probably benign Het
Stkld1 A G 2: 26,836,668 (GRCm39) N278S probably benign Het
Taar7d T A 10: 23,903,495 (GRCm39) F126I probably benign Het
Tbc1d31 A G 15: 57,824,345 (GRCm39) E869G possibly damaging Het
Tbcd C T 11: 121,384,711 (GRCm39) T315M probably benign Het
Terf2 T C 8: 107,809,656 (GRCm39) K221E possibly damaging Het
Thsd7a T A 6: 12,468,962 (GRCm39) T539S Het
Tll2 A G 19: 41,077,313 (GRCm39) F818L possibly damaging Het
Tmem87a T C 2: 120,200,959 (GRCm39) T427A possibly damaging Het
Ush2a C A 1: 188,183,952 (GRCm39) Q1419K possibly damaging Het
Vill T A 9: 118,895,821 (GRCm39) F511Y probably damaging Het
Virma T A 4: 11,542,128 (GRCm39) D1521E probably benign Het
Vps13c A G 9: 67,766,072 (GRCm39) D63G probably benign Het
Vrk2 A G 11: 26,485,575 (GRCm39) F138L probably benign Het
Zfp710 T C 7: 79,735,775 (GRCm39) I514T probably damaging Het
Zgrf1 T A 3: 127,357,032 (GRCm39) F753I possibly damaging Het
Other mutations in Or1j11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01296:Or1j11 APN 2 36,311,716 (GRCm39) missense probably benign 0.44
IGL01447:Or1j11 APN 2 36,311,466 (GRCm39) missense probably damaging 0.97
IGL01845:Or1j11 APN 2 36,312,105 (GRCm39) missense probably benign 0.27
IGL02728:Or1j11 APN 2 36,312,156 (GRCm39) missense possibly damaging 0.95
IGL02941:Or1j11 APN 2 36,312,132 (GRCm39) missense probably damaging 1.00
R0128:Or1j11 UTSW 2 36,312,299 (GRCm39) missense probably benign 0.16
R0130:Or1j11 UTSW 2 36,312,299 (GRCm39) missense probably benign 0.16
R1432:Or1j11 UTSW 2 36,311,655 (GRCm39) missense probably damaging 1.00
R1451:Or1j11 UTSW 2 36,311,877 (GRCm39) missense probably benign 0.01
R1656:Or1j11 UTSW 2 36,311,658 (GRCm39) missense probably benign 0.00
R1854:Or1j11 UTSW 2 36,311,886 (GRCm39) missense probably damaging 0.97
R2012:Or1j11 UTSW 2 36,311,931 (GRCm39) missense probably benign 0.00
R2093:Or1j11 UTSW 2 36,311,941 (GRCm39) missense probably benign 0.00
R2136:Or1j11 UTSW 2 36,311,950 (GRCm39) missense probably damaging 1.00
R2282:Or1j11 UTSW 2 36,312,012 (GRCm39) missense probably benign 0.00
R4363:Or1j11 UTSW 2 36,311,544 (GRCm39) missense probably damaging 1.00
R4466:Or1j11 UTSW 2 36,312,308 (GRCm39) missense probably benign 0.00
R4628:Or1j11 UTSW 2 36,311,869 (GRCm39) nonsense probably null
R4839:Or1j11 UTSW 2 36,312,012 (GRCm39) missense probably benign 0.00
R6023:Or1j11 UTSW 2 36,311,523 (GRCm39) missense probably damaging 0.98
R6305:Or1j11 UTSW 2 36,311,634 (GRCm39) missense probably damaging 1.00
R6486:Or1j11 UTSW 2 36,311,556 (GRCm39) missense probably damaging 1.00
R6851:Or1j11 UTSW 2 36,311,832 (GRCm39) missense probably damaging 0.97
R6864:Or1j11 UTSW 2 36,311,832 (GRCm39) missense probably damaging 0.97
R7771:Or1j11 UTSW 2 36,312,156 (GRCm39) missense possibly damaging 0.95
R8307:Or1j11 UTSW 2 36,312,333 (GRCm39) missense probably benign 0.03
R8961:Or1j11 UTSW 2 36,312,177 (GRCm39) missense probably damaging 1.00
R9152:Or1j11 UTSW 2 36,311,439 (GRCm39) missense possibly damaging 0.90
R9179:Or1j11 UTSW 2 36,312,126 (GRCm39) missense probably damaging 1.00
R9544:Or1j11 UTSW 2 36,311,784 (GRCm39) missense probably damaging 1.00
R9588:Or1j11 UTSW 2 36,311,784 (GRCm39) missense probably damaging 1.00
R9690:Or1j11 UTSW 2 36,311,530 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TACCTGACAACTGTGCTGGG -3'
(R):5'- TTCTAAAGTGAGATAGGCGAGCC -3'

Sequencing Primer
(F):5'- GGAACCTGCTCATCATCCTAC -3'
(R):5'- CCAAGAGAAGGGTGTGCGC -3'
Posted On 2020-07-13