Incidental Mutation 'R7943:Olfr168'
ID612605
Institutional Source Beutler Lab
Gene Symbol Olfr168
Ensembl Gene ENSMUSG00000061361
Gene Nameolfactory receptor 168
SynonymsMOR271-1, GA_x54KRFPKG5P-15979009-15978071
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.076) question?
Stock #R7943 (G1)
Quality Score225.009
Status Not validated
Chromosome16
Chromosomal Location19529274-19535555 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 19530417 bp
ZygosityHeterozygous
Amino Acid Change Cysteine to Serine at position 168 (C168S)
Ref Sequence ENSEMBL: ENSMUSP00000149405 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000078554] [ENSMUST00000213480]
Predicted Effect probably damaging
Transcript: ENSMUST00000078554
AA Change: C168S

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000077632
Gene: ENSMUSG00000061361
AA Change: C168S

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 damaging
Transcript: ENSMUST00000213480
AA Change: C168S

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.5%
  • 20x: 98.3%
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: 77 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930590J08Rik A G 6: 91,928,726 T493A probably damaging Het
Aars A G 8: 111,049,861 K650E probably benign Het
Abcb1b C T 5: 8,832,258 S793F probably benign Het
Adamts18 T A 8: 113,775,276 I318F probably damaging Het
Adcy8 A G 15: 64,699,473 I1137T probably damaging Het
Ambra1 T A 2: 91,773,493 F607L probably benign Het
Ankrd46 A T 15: 36,479,420 V175D possibly damaging Het
Arhgap28 C A 17: 67,901,282 E114* probably null Het
Arrdc1 C T 2: 24,926,146 G282S probably damaging Het
Atp1a3 A T 7: 24,981,791 L790Q probably damaging Het
Bend5 T A 4: 111,415,209 V12D probably damaging Het
Bod1l C T 5: 41,819,265 E1569K probably damaging Het
Cdc123 T A 2: 5,803,964 I234L probably benign Het
Cep126 T G 9: 8,120,748 E91D probably damaging Het
Cep89 T A 7: 35,414,145 D199E possibly damaging Het
Ces1d T C 8: 93,171,137 T442A probably benign Het
Chsy3 C T 18: 59,409,227 A479V probably benign Het
Clcn4 C A 7: 7,293,061 G261C probably damaging Het
Clhc1 A T 11: 29,557,651 probably null Het
Cnot3 T A 7: 3,655,566 probably null Het
Col9a1 C A 1: 24,237,180 P723H probably damaging Het
Crybg3 A T 16: 59,555,242 M169K probably benign Het
Cxxc4 A G 3: 134,258,053 R353G probably benign Het
Dennd3 A T 15: 73,540,808 I440F probably damaging Het
Elmo3 G T 8: 105,309,017 S553I probably damaging Het
Elovl2 A G 13: 41,187,467 Y198H probably benign Het
Epm2aip1 A G 9: 111,272,037 Y26C probably damaging Het
Ext1 A C 15: 53,089,939 C510G possibly damaging Het
Extl3 A T 14: 65,077,489 D81E probably benign Het
Fbxl5 T A 5: 43,758,676 T465S probably benign Het
Gabrr2 A T 4: 33,081,470 K169* probably null Het
Gm10436 A T 12: 88,176,352 N360K possibly damaging Het
Haus4 A G 14: 54,542,145 Y341H probably damaging Het
Itgae A T 11: 73,120,273 probably null Het
Jmjd7 C T 2: 120,030,515 H149Y possibly damaging Het
Kcnh2 C T 5: 24,324,563 C725Y probably damaging Het
Mroh1 C T 15: 76,447,332 P1252L probably benign Het
Ms4a14 A G 19: 11,302,944 F750S probably benign Het
Naf1 T A 8: 66,860,513 D49E unknown Het
Notch3 T C 17: 32,122,773 T2002A possibly damaging Het
Olfr1413 G A 1: 92,574,088 D306N probably benign Het
Olfr1495 T A 19: 13,768,352 D3E probably benign Het
Olfr301 A G 7: 86,407,911 probably benign Het
Olfr393 A T 11: 73,847,507 I206N probably benign Het
Olfr709-ps1 A T 7: 106,926,570 D296E probably benign Het
Olfr869 A T 9: 20,137,575 N153I probably benign Het
Pck1 A G 2: 173,155,950 T271A possibly damaging Het
Penk A G 4: 4,133,976 W224R possibly damaging Het
Per2 C A 1: 91,444,759 V198F probably damaging Het
Phf11d A G 14: 59,361,831 M23T probably damaging Het
Pla2g4d A G 2: 120,266,730 V796A probably benign Het
Prdx6 A T 1: 161,241,858 probably null Het
Prep A T 10: 45,091,012 N47I probably damaging Het
Prss38 G T 11: 59,375,170 H96N probably damaging Het
Rab11a C A 9: 64,728,331 E47* probably null Het
Rad18 C T 6: 112,649,837 G369D probably benign Het
Rragc T C 4: 123,929,924 V330A probably damaging Het
Serpina9 A T 12: 104,001,421 H238Q probably benign Het
Serpinb3b T A 1: 107,157,737 K91N probably damaging Het
Slc16a12 T G 19: 34,675,330 S139R probably benign Het
Slc22a27 T A 19: 7,910,107 probably null Het
Slc25a11 A G 11: 70,645,179 V243A probably benign Het
Slc38a9 A T 13: 112,731,614 I545F probably benign Het
Slc39a8 A T 3: 135,884,396 H349L probably damaging Het
Slk C T 19: 47,642,071 T1227I possibly damaging Het
Spdye4b A G 5: 143,194,854 E25G possibly damaging Het
St3gal1 A G 15: 67,111,265 V214A probably benign Het
St7l T A 3: 104,926,577 M550K probably benign Het
Tbk1 A C 10: 121,552,246 F638C possibly damaging Het
Tex101 A T 7: 24,669,765 C114S probably damaging Het
Ttll13 A G 7: 80,255,387 M384V probably benign Het
Ugt2b37 A T 5: 87,254,330 D147E probably damaging Het
Vmn1r10 A T 6: 57,113,701 T93S probably benign Het
Wasl G A 6: 24,619,397 P375S unknown Het
Wdr63 A G 3: 146,066,920 L457P probably damaging Het
Zfp236 C A 18: 82,674,356 E165* probably null Het
Zfp839 A T 12: 110,855,626 R291S 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
R4631:Olfr168 UTSW 16 19530141 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
R7439:Olfr168 UTSW 16 19530900 missense probably benign 0.03
R7723:Olfr168 UTSW 16 19530608 nonsense probably null
R7860:Olfr168 UTSW 16 19530417 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- AGCATGTGGTGAAGGCCTTC -3'
(R):5'- TTGACCATGGCAGGTTCTG -3'

Sequencing Primer
(F):5'- CTTTTGAGCGCATGTGGAAGACAG -3'
(R):5'- CATGGCAGGTTCTGAGGGC -3'
Posted On2019-12-27