Incidental Mutation 'R7439:Olfr168'
ID 576856
Institutional Source Beutler Lab
Gene Symbol Olfr168
Ensembl Gene ENSMUSG00000061361
Gene Name olfactory receptor 168
Synonyms MOR271-1, GA_x54KRFPKG5P-15979009-15978071
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.085) question?
Stock # R7439 (G1)
Quality Score 225.009
Status Not validated
Chromosome 16
Chromosomal Location 19529274-19535555 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to G at 19530900 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Serine to Arginine at position 7 (S7R)
Ref Sequence ENSEMBL: ENSMUSP00000149405 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000078554] [ENSMUST00000213480]
AlphaFold Q8VF05
Predicted Effect probably benign
Transcript: ENSMUST00000078554
AA Change: S7R

PolyPhen 2 Score 0.028 (Sensitivity: 0.95; Specificity: 0.81)
SMART Domains Protein: ENSMUSP00000077632
Gene: ENSMUSG00000061361
AA Change: S7R

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 benign
Transcript: ENSMUST00000213480
AA Change: S7R

PolyPhen 2 Score 0.028 (Sensitivity: 0.95; Specificity: 0.81)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.4%
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: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9530003J23Rik G A 10: 117,238,697 probably benign Het
Acacb T C 5: 114,195,642 V542A possibly damaging Het
Adprhl1 C T 8: 13,223,069 V1230I probably benign Het
Agpat1 T A 17: 34,610,909 Y77N probably damaging Het
Apc T A 18: 34,312,073 I674K probably damaging Het
Arpc5 T C 1: 152,771,436 S97P probably damaging Het
Arrdc5 A G 17: 56,297,931 F119L probably benign Het
Asap1 A G 15: 64,130,256 V402A probably damaging Het
Aspg T C 12: 112,124,821 V479A possibly damaging Het
B3galnt2 G A 13: 13,994,485 V368M probably benign Het
Bcl3 T C 7: 19,822,611 T23A probably benign Het
Bpifb5 A G 2: 154,228,933 K215E possibly damaging Het
Coa4 T A 7: 100,539,271 C64S probably damaging Het
Dcun1d4 T C 5: 73,491,536 probably null Het
Dnaaf5 T G 5: 139,166,113 C506W probably damaging Het
Dock3 A G 9: 107,023,732 Y345H probably damaging Het
Dscaml1 A G 9: 45,710,326 N1024S possibly damaging Het
Dsp T C 13: 38,176,502 probably null Het
Dsp A G 13: 38,195,449 T2057A probably benign Het
Dync1h1 T G 12: 110,636,453 L2176R probably damaging Het
Eif5b A C 1: 38,051,637 D1192A probably benign Het
Epn2 A T 11: 61,546,848 probably benign Het
Exoc1 T A 5: 76,545,348 N360K probably benign Het
Fam135b A T 15: 71,463,680 V555E probably damaging Het
Fam208a T A 14: 27,471,645 V934E probably damaging Het
Fmn1 A T 2: 113,441,611 Q108L unknown Het
Gcc2 A G 10: 58,256,901 T48A probably benign Het
Gm438 T C 4: 144,777,762 D273G probably damaging Het
Gm6619 T G 6: 131,490,391 I73S possibly damaging Het
Gm8267 T A 14: 44,722,940 D116V probably damaging Het
Hapln3 T A 7: 79,117,269 T341S probably benign Het
Lamb3 C A 1: 193,332,166 D544E possibly damaging Het
Lhx5 T A 5: 120,440,284 S390T probably benign Het
Lrrc63 A G 14: 75,126,257 S145P possibly damaging Het
Lrriq1 T C 10: 103,214,519 M791V probably benign Het
Lyg2 A G 1: 37,911,137 Y37H possibly damaging Het
Nrbp1 T A 5: 31,244,956 M172K probably damaging Het
Olfr1044 T A 2: 86,171,010 D269V probably damaging Het
Olfr1261 A G 2: 89,993,839 I149V probably benign Het
Pcyt2 A T 11: 120,611,383 Y308N possibly damaging Het
Peg10 C CTCA 6: 4,756,453 probably benign Het
Phf21b A G 15: 84,804,903 S141P probably damaging Het
Pigh G A 12: 79,089,550 P24S probably benign Het
Plekhg3 A G 12: 76,576,485 D834G probably damaging Het
Plekhg5 T A 4: 152,113,935 V860D probably benign Het
Pon1 A G 6: 5,177,399 I170T probably damaging Het
Ptpn9 T A 9: 57,027,433 Y160* probably null Het
Ptprj T C 2: 90,449,819 K1045R possibly damaging Het
Rilpl2 T A 5: 124,463,788 H196L probably benign Het
Rnf112 C T 11: 61,451,028 V317I possibly damaging Het
Rundc3a G T 11: 102,400,046 probably null Het
Sgsm1 T C 5: 113,274,321 Y489C probably damaging Het
Sis G A 3: 72,909,041 H1531Y possibly damaging Het
Slc26a9 A G 1: 131,762,818 Y520C probably damaging Het
Smc5 A G 19: 23,242,700 V467A probably damaging Het
Spata20 G A 11: 94,484,041 A245V probably benign Het
Steap3 A C 1: 120,241,518 F350V probably benign Het
Sucnr1 A G 3: 60,086,696 Q215R probably benign Het
Supv3l1 G A 10: 62,430,615 A594V probably damaging Het
Swt1 A T 1: 151,411,064 F226I probably benign Het
Taar7f A G 10: 24,049,987 T160A possibly damaging Het
Tada2a A T 11: 84,126,986 probably null Het
Taok3 C A 5: 117,250,909 Q460K probably damaging Het
Twf2 A G 9: 106,214,398 E268G probably damaging Het
Upf2 A T 2: 6,018,932 I698F unknown Het
Vmn2r35 T A 7: 7,817,014 N86Y probably damaging Het
Vmn2r84 T C 10: 130,392,113 T85A possibly damaging Het
Vps13d A G 4: 145,105,856 S2833P Het
Xrn1 T C 9: 96,051,629 S1584P probably benign Het
Zfp354b T C 11: 50,922,397 Y567C probably damaging Het
Zfp52 A T 17: 21,560,870 R327* probably null 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
R7723:Olfr168 UTSW 16 19530608 nonsense probably null
R7860:Olfr168 UTSW 16 19530417 missense probably damaging 1.00
R8871:Olfr168 UTSW 16 19530786 missense
R9515:Olfr168 UTSW 16 19530276 missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TGTACATCAGGTCCATGAGAGAG -3'
(R):5'- GAATTGTGATCATGGCCAGGG -3'

Sequencing Primer
(F):5'- TCCATGAGAGAGAGCTGACTG -3'
(R):5'- CCAGGGAAGAAACATTCAGTTC -3'
Posted On 2019-10-07