Incidental Mutation 'R6197:Or10v9'
ID 503009
Institutional Source Beutler Lab
Gene Symbol Or10v9
Ensembl Gene ENSMUSG00000060556
Gene Name olfactory receptor family 10 subfamily V member 9
Synonyms GA_x6K02T2RE5P-2207258-2206302, Olfr1418, MOR266-5
MMRRC Submission 044337-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.056) question?
Stock # R6197 (G1)
Quality Score 225.009
Status Not validated
Chromosome 19
Chromosomal Location 11832359-11833315 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 11833148 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Glutamine at position 56 (H56Q)
Ref Sequence ENSEMBL: ENSMUSP00000150146 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000079875] [ENSMUST00000214796]
AlphaFold Q7TQS3
Predicted Effect probably damaging
Transcript: ENSMUST00000079875
AA Change: H56Q

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000078800
Gene: ENSMUSG00000060556
AA Change: H56Q

DomainStartEndE-ValueType
Pfam:7tm_4 31 309 4.2e-53 PFAM
Pfam:7tm_1 41 291 5.4e-22 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000214796
AA Change: H56Q

PolyPhen 2 Score 0.990 (Sensitivity: 0.72; Specificity: 0.97)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.7%
Validation Efficiency 92% (49/53)
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: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700109H08Rik T A 5: 3,630,442 (GRCm39) Y119* probably null Het
Abcb9 C A 5: 124,209,812 (GRCm39) E664* probably null Het
Adgrl2 T C 3: 148,564,578 (GRCm39) D334G probably damaging Het
Ak9 T G 10: 41,193,826 (GRCm39) C57G probably damaging Het
Als2cl A G 9: 110,724,952 (GRCm39) K809E probably damaging Het
Arsi G A 18: 61,049,723 (GRCm39) G202E probably benign Het
Atp11a A G 8: 12,896,099 (GRCm39) I223V probably benign Het
Cacna2d3 A T 14: 28,630,278 (GRCm39) V1022E probably benign Het
Cc2d1b C T 4: 108,490,422 (GRCm39) R825W probably damaging Het
Cd37 A G 7: 44,886,598 (GRCm39) C85R probably damaging Het
Ces1g T C 8: 94,063,764 (GRCm39) S7G probably benign Het
Cltc T C 11: 86,611,188 (GRCm39) N561S probably benign Het
Cnbd2 A G 2: 156,217,494 (GRCm39) E661G possibly damaging Het
Col6a3 A T 1: 90,750,063 (GRCm39) F257Y probably damaging Het
Cpt1b T C 15: 89,309,037 (GRCm39) Y55C possibly damaging Het
Csmd1 A G 8: 15,976,611 (GRCm39) V2869A probably benign Het
Dnah11 T C 12: 118,143,482 (GRCm39) E387G probably benign Het
Eny2 T A 15: 44,292,949 (GRCm39) probably null Het
Fbxo10 G T 4: 45,043,857 (GRCm39) H655Q probably benign Het
Gm14403 AAACCCTA AA 2: 177,201,448 (GRCm39) probably benign Het
Gpx2 C T 12: 76,842,068 (GRCm39) G28S probably damaging Het
H2-Q5 G T 17: 35,613,918 (GRCm39) A156S probably benign Het
Hoxd4 A G 2: 74,558,807 (GRCm39) D210G possibly damaging Het
Hoxd9 A G 2: 74,529,166 (GRCm39) Q256R probably damaging Het
Macf1 A G 4: 123,346,085 (GRCm39) V2571A probably damaging Het
Mtus1 A G 8: 41,537,074 (GRCm39) V214A possibly damaging Het
Myh1 C T 11: 67,111,793 (GRCm39) A1716V probably benign Het
Nbeal1 A G 1: 60,261,287 (GRCm39) D249G probably damaging Het
Nup54 TCTGCTGCTGCTGCTGCTGCTGCTG TCTGCTGCTGCTGCTGCTGCTG 5: 92,578,663 (GRCm39) probably benign Het
Or4c124 A T 2: 89,155,677 (GRCm39) N282K probably damaging Het
Or5w17 C T 2: 87,583,696 (GRCm39) V214I probably benign Het
Or7a37 T G 10: 78,805,974 (GRCm39) L164V probably damaging Het
Peg10 GC GCTCC 6: 4,756,452 (GRCm39) probably benign Het
Pramel23 T C 4: 143,423,886 (GRCm39) Y301C possibly damaging Het
Prss59 A G 6: 40,897,939 (GRCm39) I248T probably benign Het
Pwwp2a A G 11: 43,595,423 (GRCm39) D196G probably benign Het
Rarg A T 15: 102,150,327 (GRCm39) C93S possibly damaging Het
Rcc1 T C 4: 132,065,073 (GRCm39) D150G possibly damaging Het
Ripk2 A G 4: 16,163,330 (GRCm39) Y23H probably damaging Het
Rragc A G 4: 123,811,340 (GRCm39) Y5C possibly damaging Het
Rubcnl G A 14: 75,269,369 (GRCm39) G9D probably damaging Het
Sephs2 A T 7: 126,872,073 (GRCm39) V340E probably damaging Het
Slc22a3 C T 17: 12,677,438 (GRCm39) M243I probably benign Het
Slco6c1 A G 1: 97,000,518 (GRCm39) probably null Het
Sncaip T G 18: 53,039,966 (GRCm39) I308R probably damaging Het
Supt16 G A 14: 52,408,338 (GRCm39) T869M probably damaging Het
Tanc1 G A 2: 59,674,366 (GRCm39) E1817K possibly damaging Het
Usp4 C A 9: 108,248,154 (GRCm39) Q395K probably damaging Het
Usp49 T A 17: 47,984,272 (GRCm39) S210T possibly damaging Het
Virma A G 4: 11,505,498 (GRCm39) I124M probably damaging Het
Vmn1r234 G A 17: 21,449,589 (GRCm39) V168I probably benign Het
Vnn3 T A 10: 23,732,187 (GRCm39) C146S probably damaging Het
Ylpm1 A G 12: 85,088,953 (GRCm39) D1234G probably damaging Het
Zfp617 T A 8: 72,687,098 (GRCm39) V476E probably benign Het
Other mutations in Or10v9
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0638:Or10v9 UTSW 19 11,832,732 (GRCm39) missense probably damaging 0.97
R0638:Or10v9 UTSW 19 11,832,487 (GRCm39) missense probably damaging 1.00
R1882:Or10v9 UTSW 19 11,832,835 (GRCm39) missense probably damaging 1.00
R1981:Or10v9 UTSW 19 11,832,371 (GRCm39) missense possibly damaging 0.65
R3896:Or10v9 UTSW 19 11,832,951 (GRCm39) missense probably damaging 1.00
R4853:Or10v9 UTSW 19 11,832,645 (GRCm39) missense probably benign
R4904:Or10v9 UTSW 19 11,833,231 (GRCm39) missense possibly damaging 0.92
R5385:Or10v9 UTSW 19 11,832,541 (GRCm39) missense probably damaging 1.00
R7138:Or10v9 UTSW 19 11,832,652 (GRCm39) missense probably damaging 1.00
R8114:Or10v9 UTSW 19 11,832,466 (GRCm39) missense probably damaging 1.00
R8524:Or10v9 UTSW 19 11,832,445 (GRCm39) missense probably damaging 1.00
R9139:Or10v9 UTSW 19 11,832,666 (GRCm39) missense probably damaging 0.97
R9627:Or10v9 UTSW 19 11,832,910 (GRCm39) missense possibly damaging 0.83
Z1177:Or10v9 UTSW 19 11,832,536 (GRCm39) nonsense probably null
Predicted Primers PCR Primer
(F):5'- GTGACAGATGGCCACAAACC -3'
(R):5'- CCAACGCATTAAGTTCATGGAGG -3'

Sequencing Primer
(F):5'- TGGCCACAAACCGGTCATAGG -3'
(R):5'- CATTAAGTTCATGGAGGAAGGAAATC -3'
Posted On 2018-02-27