Incidental Mutation 'R6864:Or1j11'
ID 535787
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 044964-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.102) question?
Stock # R6864 (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 36311832 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Serine at position 141 (C141S)
Ref Sequence ENSEMBL: ENSMUSP00000149068 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071437] [ENSMUST00000216645]
AlphaFold Q8VGK8
Predicted Effect probably damaging
Transcript: ENSMUST00000071437
AA Change: C141S

PolyPhen 2 Score 0.970 (Sensitivity: 0.77; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000071383
Gene: ENSMUSG00000094464
AA Change: C141S

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 3.9e-55 PFAM
Pfam:7tm_1 41 290 5e-24 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000216645
AA Change: C141S

PolyPhen 2 Score 0.970 (Sensitivity: 0.77; Specificity: 0.96)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.2%
  • 20x: 97.2%
Validation Efficiency 100% (60/60)
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: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgre1 C T 17: 57,785,879 (GRCm39) T875I probably damaging Het
Anln A T 9: 22,293,545 (GRCm39) S33T probably benign Het
Anxa6 T C 11: 54,877,011 (GRCm39) T541A probably benign Het
Atxn2 C T 5: 121,917,557 (GRCm39) R334W probably damaging Het
AU040320 T A 4: 126,741,612 (GRCm39) V940D probably damaging Het
Bcl2 A T 1: 106,471,011 (GRCm39) Y232N probably damaging Het
Bmp7 A G 2: 172,781,855 (GRCm39) V3A probably benign Het
Calr A T 8: 85,571,557 (GRCm39) H145Q probably damaging Het
Camta2 T A 11: 70,562,792 (GRCm39) T976S probably benign Het
Ccnk G A 12: 108,168,473 (GRCm39) probably benign Het
Cntln T C 4: 85,015,029 (GRCm39) S1107P probably damaging Het
Cradd T C 10: 95,011,789 (GRCm39) D117G probably damaging Het
Dcaf7 C T 11: 105,937,647 (GRCm39) T90I probably damaging Het
Defb30 T A 14: 63,273,552 (GRCm39) probably null Het
Dock4 T A 12: 40,795,745 (GRCm39) I854N probably damaging Het
Dym T A 18: 75,189,809 (GRCm39) Y132* probably null Het
Eef1a2 T C 2: 180,791,477 (GRCm39) T341A probably benign Het
Eml2 T C 7: 18,930,206 (GRCm39) V309A probably damaging Het
Flnb C T 14: 7,905,640 (GRCm38) P1130L possibly damaging Het
Hivep3 C A 4: 119,952,085 (GRCm39) Q134K possibly damaging Het
Kbtbd2 T A 6: 56,757,011 (GRCm39) K242* probably null Het
Kel A G 6: 41,680,694 (GRCm39) probably null Het
Lcorl T A 5: 45,904,546 (GRCm39) K177N probably damaging Het
Mbd3l2 A G 9: 18,354,795 (GRCm39) probably benign Het
Mcm3ap A G 10: 76,343,313 (GRCm39) D1735G probably damaging Het
Ms4a1 C A 19: 11,230,542 (GRCm39) probably null Het
Muc5ac C T 7: 141,363,481 (GRCm39) probably benign Het
Mylk C A 16: 34,694,520 (GRCm39) P193Q probably benign Het
Or2y16 G T 11: 49,334,767 (GRCm39) A30S probably benign Het
Or2y17 A T 11: 49,231,580 (GRCm39) T74S probably damaging Het
Or4d10b A T 19: 12,036,777 (GRCm39) F113Y probably damaging Het
Or4f52 C T 2: 111,061,542 (GRCm39) V199I probably benign Het
Otogl C T 10: 107,663,667 (GRCm39) S968N probably damaging Het
Oxr1 T G 15: 41,686,783 (GRCm39) V555G probably damaging Het
Parp12 T C 6: 39,088,670 (GRCm39) I189V probably benign Het
Peg3 T C 7: 6,715,761 (GRCm39) Y103C probably damaging Het
Plekhh2 T C 17: 84,925,427 (GRCm39) V1408A probably benign Het
Prkacb T C 3: 146,451,133 (GRCm39) Y204C probably damaging Het
Prkch A G 12: 73,806,391 (GRCm39) E546G probably damaging Het
Prss12 C A 3: 123,241,033 (GRCm39) H76N probably benign Het
Rai14 G T 15: 10,633,254 (GRCm39) S45R possibly damaging Het
Samd9l T A 6: 3,374,750 (GRCm39) D837V probably benign Het
Slc22a6 G T 19: 8,595,805 (GRCm39) C49F probably damaging Het
Slc2a2 T A 3: 28,775,874 (GRCm39) I328N probably damaging Het
Slc35f4 T C 14: 49,556,310 (GRCm39) I148V possibly damaging Het
Stk32b A T 5: 37,606,149 (GRCm39) probably null Het
Tasor T A 14: 27,183,115 (GRCm39) F525I probably damaging Het
Tktl2 T C 8: 66,964,991 (GRCm39) I183T probably damaging Het
Tmem175 A C 5: 108,793,845 (GRCm39) H325P probably damaging Het
Tns3 A G 11: 8,443,196 (GRCm39) V389A probably damaging Het
Trappc9 A T 15: 72,809,011 (GRCm39) probably null Het
Trim28 T A 7: 12,763,385 (GRCm39) F509I possibly damaging Het
Vmn1r210 T A 13: 23,011,713 (GRCm39) Q191L probably benign Het
Vmn2r24 A T 6: 123,756,117 (GRCm39) D63V possibly damaging Het
Zfp536 A G 7: 37,267,940 (GRCm39) L492P probably damaging Het
Zfp831 C A 2: 174,488,533 (GRCm39) N1069K possibly damaging Het
Zfp943 T A 17: 22,211,593 (GRCm39) H226Q probably 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
R7771:Or1j11 UTSW 2 36,312,156 (GRCm39) missense possibly damaging 0.95
R8165:Or1j11 UTSW 2 36,311,715 (GRCm39) missense probably damaging 1.00
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'- CACTTGGCCTTCACAGACATC -3'
(R):5'- CCAGCTCATTGATGGTGGTG -3'

Sequencing Primer
(F):5'- GCTCCTAAGATGCTCGTGAATATGC -3'
(R):5'- CTCATTGATGGTGGTGTCTGAGC -3'
Posted On 2018-10-18