Incidental Mutation 'R7508:Olfr11'
ID581913
Institutional Source Beutler Lab
Gene Symbol Olfr11
Ensembl Gene ENSMUSG00000036658
Gene Nameolfactory receptor 11
SynonymsGA_x6K02T2QHY8-11597382-11598323, MOR256-11
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.178) question?
Stock #R7508 (G1)
Quality Score225.009
Status Validated
Chromosome13
Chromosomal Location21636623-21642518 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 21638609 bp
ZygosityHeterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 305 (I305F)
Ref Sequence ENSEMBL: ENSMUSP00000146091 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000043081] [ENSMUST00000205631]
Predicted Effect probably benign
Transcript: ENSMUST00000043081
AA Change: I305F

PolyPhen 2 Score 0.194 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000043099
Gene: ENSMUSG00000036658
AA Change: I305F

DomainStartEndE-ValueType
Pfam:7tm_4 31 311 4.9e-51 PFAM
Pfam:7tm_1 41 290 7.3e-27 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000205631
AA Change: I305F

PolyPhen 2 Score 0.194 (Sensitivity: 0.92; Specificity: 0.87)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency 100% (56/56)
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: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgra3 C T 5: 50,016,867 A110T probably benign Het
Adra1a A C 14: 66,637,935 I120L probably damaging Het
Ahnak2 C T 12: 112,774,405 V1078I possibly damaging Het
Ccser1 A G 6: 61,570,723 H590R probably benign Het
Cdh12 T G 15: 21,583,765 L564V probably benign Het
Celsr3 T A 9: 108,836,622 H1900Q probably benign Het
Clasp1 T A 1: 118,545,434 M918K probably benign Het
Cmtm6 A G 9: 114,731,240 E2G probably damaging Het
Ctsg A G 14: 56,100,541 probably null Het
Cylc2 T A 4: 51,229,256 probably null Het
Dna2 A G 10: 62,971,993 probably null Het
Dnaic1 G A 4: 41,614,323 R333H probably benign Het
Egln3 T C 12: 54,180,628 D239G probably benign Het
Fam13a A T 6: 58,987,284 D54E probably damaging Het
Fn1 A G 1: 71,597,516 V2159A probably benign Het
Gcnt2 T A 13: 40,887,681 F105L probably benign Het
Gm5788 T C 12: 87,494,842 M41T possibly damaging Het
Gpd1 G A 15: 99,722,086 S255N probably damaging Het
Hacd4 A G 4: 88,437,478 F57L probably benign Het
Helb T C 10: 120,105,283 D500G probably benign Het
Ighv1-26 G A 12: 114,788,442 S94F probably damaging Het
Kirrel T C 3: 87,083,439 D692G possibly damaging Het
Klra7 A T 6: 130,230,091 probably null Het
Lyl1 T C 8: 84,704,300 V277A probably benign Het
Mon2 A C 10: 123,023,939 W811G probably damaging Het
Myo9b T C 8: 71,354,801 L1627P probably benign Het
Neurl1b C G 17: 26,438,746 H219Q probably benign Het
Odf4 A T 11: 68,922,423 C218S possibly damaging Het
Olfr1038-ps A G 2: 86,121,938 N5S possibly damaging Het
Pde5a A G 3: 122,818,030 D571G probably damaging Het
Pgc A G 17: 47,734,186 E343G probably benign Het
Pik3cd A G 4: 149,654,583 F667L possibly damaging Het
Prf1 G A 10: 61,300,155 R70H possibly damaging Het
Ptprb C T 10: 116,353,991 Q1565* probably null Het
Rapgef4 T A 2: 72,205,733 N523K probably benign Het
Rbm25 T C 12: 83,672,877 L557P probably damaging Het
Rhobtb3 C T 13: 75,878,857 V466I probably benign Het
Rnpep A G 1: 135,278,858 V166A probably benign Het
Sgo2a A G 1: 58,017,795 K1046R probably benign Het
Slc12a2 T C 18: 57,904,393 V525A probably benign Het
Slc1a4 A T 11: 20,306,487 I448N probably damaging Het
Slc29a4 C T 5: 142,718,506 P305L probably benign Het
Slc9a5 T A 8: 105,363,253 probably null Het
Spag16 A T 1: 69,887,520 N258I possibly damaging Het
Sspo T A 6: 48,466,699 L2076Q probably damaging Het
Taok1 T A 11: 77,545,326 H704L probably damaging Het
Tbc1d9b T C 11: 50,145,120 F148L probably damaging Het
Tm4sf1 A G 3: 57,294,755 Y12H probably benign Het
Traj6 C T 14: 54,212,714 T9M Het
Ttll4 A G 1: 74,687,259 N672S possibly damaging Het
Ube3a T A 7: 59,303,689 H790Q possibly damaging Het
Usp49 G A 17: 47,672,280 R70Q probably benign Het
Vmn2r32 C T 7: 7,467,374 V515M possibly damaging Het
Wars A G 12: 108,882,875 S49P probably benign Het
Zbp1 T A 2: 173,207,811 Q386L possibly damaging Het
Zfp369 T C 13: 65,279,273 F10S unknown Het
Zfp512 C G 5: 31,473,539 I408M possibly damaging Het
Zfp952 A G 17: 33,003,782 I412V probably benign Het
Other mutations in Olfr11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02513:Olfr11 APN 13 21639340 missense probably damaging 1.00
R0513:Olfr11 UTSW 13 21638949 missense probably benign 0.26
R0928:Olfr11 UTSW 13 21638956 missense probably damaging 1.00
R1440:Olfr11 UTSW 13 21639390 missense probably benign 0.11
R1673:Olfr11 UTSW 13 21639044 missense probably damaging 1.00
R1705:Olfr11 UTSW 13 21639161 missense probably damaging 1.00
R2080:Olfr11 UTSW 13 21639436 missense probably damaging 0.99
R2187:Olfr11 UTSW 13 21639385 missense probably damaging 0.99
R2283:Olfr11 UTSW 13 21639020 missense probably damaging 1.00
R2340:Olfr11 UTSW 13 21638587 missense probably benign 0.03
R3690:Olfr11 UTSW 13 21639338 missense probably damaging 1.00
R4108:Olfr11 UTSW 13 21638782 missense probably damaging 1.00
R4739:Olfr11 UTSW 13 21639170 missense possibly damaging 0.90
R4740:Olfr11 UTSW 13 21639170 missense possibly damaging 0.90
R5335:Olfr11 UTSW 13 21638779 missense probably damaging 1.00
R5790:Olfr11 UTSW 13 21638876 missense probably benign
R6320:Olfr11 UTSW 13 21639248 missense probably damaging 1.00
R7406:Olfr11 UTSW 13 21639146 missense probably benign 0.16
R8054:Olfr11 UTSW 13 21638949 missense probably benign 0.26
Predicted Primers PCR Primer
(F):5'- AGGCTAGTTCAGTGTTTTCAACAAC -3'
(R):5'- CAAAAGGCGTTTGGGACCTG -3'

Sequencing Primer
(F):5'- TGTTTTCAACAACACTCTAAACTCC -3'
(R):5'- GGGACCTGTAGCTCTCATCTAATAG -3'
Posted On2019-10-17