Incidental Mutation 'R4631:Olfr168'
ID349228
Institutional Source Beutler Lab
Gene Symbol Olfr168
Ensembl Gene ENSMUSG00000061361
Gene Nameolfactory receptor 168
SynonymsMOR271-1, GA_x54KRFPKG5P-15979009-15978071
MMRRC Submission 041896-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.065) question?
Stock #R4631 (G1)
Quality Score225
Status Validated
Chromosome16
Chromosomal Location19529274-19535555 bp(-) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) G to A at 19530141 bp
ZygosityHeterozygous
Amino Acid Change Arginine to Stop codon at position 260 (R260*)
Ref Sequence ENSEMBL: ENSMUSP00000149405 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000078554] [ENSMUST00000213480]
Predicted Effect probably null
Transcript: ENSMUST00000078554
AA Change: R260*
SMART Domains Protein: ENSMUSP00000077632
Gene: ENSMUSG00000061361
AA Change: R260*

DomainStartEndE-ValueType
Pfam:7tm_4 30 306 5e-50 PFAM
Pfam:7TM_GPCR_Srsx 34 295 3.7e-8 PFAM
Pfam:7tm_1 40 289 3.6e-27 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000213480
AA Change: R260*
Meta Mutation Damage Score 0.6356 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 95.0%
Validation Efficiency 100% (84/84)
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: 77 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700017B05Rik A T 9: 57,257,987 L368Q probably damaging Het
Abcc2 C T 19: 43,814,707 P661S possibly damaging Het
Adgre4 T G 17: 55,814,305 M457R probably null Het
Ank C A 15: 27,467,090 F29L probably benign Het
Arhgap20 T C 9: 51,840,353 probably benign Het
Atf6 T C 1: 170,747,197 probably null Het
Bod1l A G 5: 41,817,735 F2079L probably damaging Het
Cd163 T C 6: 124,329,086 *1122Q probably null Het
Ces2g T C 8: 104,967,462 probably null Het
Cntnap3 A G 13: 64,778,883 Y558H probably benign Het
Ctsm T A 13: 61,537,696 S301C probably null Het
Dlc1 A C 8: 36,937,558 probably null Het
Dlg2 A T 7: 92,088,614 I435F probably damaging Het
Dnah5 T C 15: 28,401,953 V3420A probably damaging Het
Dnah5 T A 15: 28,419,994 Y3813N probably damaging Het
Dnajc13 A G 9: 104,190,417 M1181T probably damaging Het
Drc3 C A 11: 60,364,908 T107N probably benign Het
Dydc2 T C 14: 41,049,329 E131G probably benign Het
Eif5b T C 1: 38,041,747 V723A probably damaging Het
Fndc9 C A 11: 46,237,848 H65N possibly damaging Het
Fzd1 A T 5: 4,755,865 Y572* probably null Het
Gm1966 A G 7: 106,599,523 noncoding transcript Het
Gm38394 A T 1: 133,658,744 V285E probably damaging Het
Gm5096 G A 18: 87,756,401 R16H probably damaging Het
Gps1 T A 11: 120,788,239 probably null Het
Kazn G A 4: 142,118,160 probably benign Het
Kcnd3 C T 3: 105,658,766 A421V probably damaging Het
Kcnip1 T A 11: 33,992,821 noncoding transcript Het
Kif19a A G 11: 114,784,847 I382V possibly damaging Het
Krt1 C T 15: 101,846,187 G543S unknown Het
Malsu1 A T 6: 49,084,533 E177V probably damaging Het
Man2a2 A G 7: 80,362,463 F649L probably benign Het
Map3k11 A G 19: 5,690,913 I223V probably benign Het
Mroh2a A G 1: 88,258,664 S64G probably benign Het
Myh9 T G 15: 77,797,028 D164A probably damaging Het
Myo16 T C 8: 10,506,984 I1040T probably damaging Het
Myo18b C T 5: 112,846,400 A896T probably damaging Het
Myocd G T 11: 65,178,859 N798K probably benign Het
Olfr1206 C T 2: 88,864,830 T75I probably benign Het
Olfr1288 T A 2: 111,479,563 W260R probably damaging Het
Olfr1458 T A 19: 13,103,272 I11F probably benign Het
Olfr156 T C 4: 43,820,563 D266G probably benign Het
Olfr353 T G 2: 36,890,618 T77P probably benign Het
Olfr68 A T 7: 103,777,475 L290Q probably damaging Het
Pcdh18 T A 3: 49,756,441 I142F probably damaging Het
Pcyox1 T C 6: 86,389,143 D363G probably benign Het
Pcyox1 T C 6: 86,389,230 E334G possibly damaging Het
Pgm1 A G 5: 64,105,947 probably null Het
Plagl1 T G 10: 13,127,999 probably benign Het
Ppp1r9a A G 6: 4,906,537 D364G possibly damaging Het
Rab2b T A 14: 52,266,242 H141L possibly damaging Het
Rev3l A G 10: 39,828,416 K279E probably benign Het
Rnf111 G T 9: 70,450,396 T607N probably benign Het
Scn8a C A 15: 101,016,503 S1130* probably null Het
Selenbp1 A G 3: 94,944,568 *473W probably null Het
Sh3bp4 A C 1: 89,144,273 D281A probably damaging Het
Skint5 T A 4: 113,629,117 probably null Het
Slc1a4 A G 11: 20,308,452 L249P probably damaging Het
Slc45a2 T A 15: 11,012,576 S222T probably benign Het
Slc7a4 A G 16: 17,574,391 F393S probably damaging Het
Slc9a2 A T 1: 40,761,918 D536V possibly damaging Het
Stra6 T A 9: 58,140,832 probably benign Het
Tmem145 A G 7: 25,307,825 D156G probably benign Het
Tns3 A C 11: 8,451,119 F1060V probably benign Het
Trak1 G A 9: 121,454,425 R419Q probably benign Het
Trappc8 A G 18: 20,867,808 S273P probably benign Het
Trmt11 A G 10: 30,559,204 S320P probably benign Het
Ugt1a6a A T 1: 88,139,258 Y262F probably benign Het
Vmn1r73 G A 7: 11,756,831 C192Y probably benign Het
Vmn2r103 T C 17: 19,793,696 I250T probably benign Het
Vmn2r25 T A 6: 123,853,003 D63V possibly damaging Het
Vps13b C T 15: 35,646,132 H1461Y possibly damaging Het
Ythdc2 A T 18: 44,887,631 E1427D probably benign Het
Zbtb26 A G 2: 37,436,956 F23L probably benign Het
Zfp62 T A 11: 49,217,805 *908R probably null Het
Zfp975 A T 7: 42,662,945 N81K probably benign Het
Zkscan16 G A 4: 58,951,918 V198M probably damaging Het
Other mutations in Olfr168
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01635:Olfr168 APN 16 19530095 missense probably benign 0.13
IGL02139:Olfr168 APN 16 19530890 missense probably benign 0.05
IGL02347:Olfr168 APN 16 19530779 missense probably damaging 1.00
IGL03402:Olfr168 APN 16 19530917 start codon destroyed probably null 0.99
R0542:Olfr168 UTSW 16 19529982 makesense probably null
R1496:Olfr168 UTSW 16 19530383 missense possibly damaging 0.94
R1707:Olfr168 UTSW 16 19530177 missense probably benign 0.18
R2006:Olfr168 UTSW 16 19530705 missense probably benign 0.02
R2220:Olfr168 UTSW 16 19530145 nonsense probably null
R3734:Olfr168 UTSW 16 19530648 missense probably damaging 0.99
R4134:Olfr168 UTSW 16 19530702 missense possibly damaging 0.90
R4135:Olfr168 UTSW 16 19530702 missense possibly damaging 0.90
R4538:Olfr168 UTSW 16 19530631 nonsense probably null
R4633:Olfr168 UTSW 16 19530284 missense possibly damaging 0.94
R4872:Olfr168 UTSW 16 19530633 missense probably damaging 0.99
R4910:Olfr168 UTSW 16 19530018 missense probably benign 0.03
R4945:Olfr168 UTSW 16 19530557 missense probably benign 0.03
R5345:Olfr168 UTSW 16 19530777 missense probably damaging 1.00
R5847:Olfr168 UTSW 16 19530326 missense probably damaging 0.99
R5899:Olfr168 UTSW 16 19530801 missense probably damaging 1.00
R7074:Olfr168 UTSW 16 19530105 missense possibly damaging 0.90
Predicted Primers PCR Primer
(F):5'- GGCACACATTGTATTTCCAACAGAC -3'
(R):5'- AGCACAAGCCTGTTTCTCC -3'

Sequencing Primer
(F):5'- TTCCAACAGACAACACAAGTTTATG -3'
(R):5'- AGCACAAGCCTGTTTCTCCTACTG -3'
Posted On2015-10-08