Incidental Mutation 'R3896:Or10v9'
ID 310567
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 040807-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.056) question?
Stock # R3896 (G1)
Quality Score 225
Status Validated
Chromosome 19
Chromosomal Location 11832359-11833315 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 11832951 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 122 (D122G)
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: D122G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000078800
Gene: ENSMUSG00000060556
AA Change: D122G

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: D122G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.5%
Validation Efficiency 100% (48/48)
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: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930503B20Rik A T 3: 146,356,868 (GRCm39) N13K possibly damaging Het
Alas1 G T 9: 106,119,000 (GRCm39) probably null Het
Arhgap20 A T 9: 51,728,137 (GRCm39) I117F probably damaging Het
Asz1 A G 6: 18,075,766 (GRCm39) I269T probably benign Het
Atp8a2 C A 14: 60,263,589 (GRCm39) probably null Het
Atp8b2 A T 3: 89,864,626 (GRCm39) I163K probably damaging Het
Casd1 T A 6: 4,640,980 (GRCm39) F700L probably damaging Het
Ccdc80 A G 16: 44,916,984 (GRCm39) D580G probably benign Het
Cog7 C T 7: 121,540,392 (GRCm39) probably benign Het
Cyp2c66 T C 19: 39,130,722 (GRCm39) V112A possibly damaging Het
D130040H23Rik T A 8: 69,755,610 (GRCm39) C356S probably damaging Het
Emb A G 13: 117,409,598 (GRCm39) *331W probably null Het
Enpp3 A C 10: 24,653,847 (GRCm39) S703R possibly damaging Het
Fam13b T C 18: 34,596,008 (GRCm39) probably benign Het
Foxp1 T A 6: 99,052,897 (GRCm39) Q97L probably benign Het
Gdf10 A T 14: 33,656,438 (GRCm39) N467Y probably damaging Het
Gm29394 C T 15: 57,912,024 (GRCm39) probably benign Het
Gsn T C 2: 35,192,650 (GRCm39) S522P possibly damaging Het
Hydin T A 8: 111,235,711 (GRCm39) F1899I possibly damaging Het
Ints1 C A 5: 139,743,399 (GRCm39) E1658* probably null Het
Jakmip2 A T 18: 43,682,751 (GRCm39) F691Y probably benign Het
Klhl28 A G 12: 65,004,333 (GRCm39) F60S probably damaging Het
Loxhd1 C T 18: 77,469,719 (GRCm39) S992L possibly damaging Het
Lrp1b A T 2: 40,812,440 (GRCm39) probably null Het
Macf1 A T 4: 123,364,987 (GRCm39) I3258N possibly damaging Het
Map4k2 G T 19: 6,391,958 (GRCm39) E91* probably null Het
Matcap1 T A 8: 106,009,920 (GRCm39) H343L probably benign Het
Myo1b A T 1: 51,812,420 (GRCm39) V739E probably damaging Het
Naa35 C T 13: 59,755,109 (GRCm39) T185I probably damaging Het
Or4c15b A G 2: 89,113,441 (GRCm39) F33S possibly damaging Het
Reg4 A T 3: 98,132,082 (GRCm39) probably benign Het
Rnaseh2b A C 14: 62,597,906 (GRCm39) probably benign Het
Rnf123 G A 9: 107,946,302 (GRCm39) probably benign Het
Scn8a A T 15: 100,933,379 (GRCm39) M1528L probably benign Het
Sdr16c5 T A 4: 4,006,609 (GRCm39) T228S probably damaging Het
Sgo2a T C 1: 58,052,805 (GRCm39) C202R probably damaging Het
Slc25a46 A G 18: 31,716,725 (GRCm39) L259P probably damaging Het
Slc4a4 A G 5: 89,345,625 (GRCm39) probably benign Het
Sox14 G T 9: 99,757,636 (GRCm39) H34Q probably damaging Het
Syna T A 5: 134,587,165 (GRCm39) K595* probably null Het
Taf4 A G 2: 179,573,807 (GRCm39) V687A probably benign Het
Tmbim7 C T 5: 3,711,916 (GRCm39) H54Y probably benign Het
Vmn1r212 T C 13: 23,068,067 (GRCm39) M89V probably benign Het
Vmn1r86 T C 7: 12,836,093 (GRCm39) Y261C probably benign Het
Xkr4 A G 1: 3,286,414 (GRCm39) I592T probably damaging Het
Ywhah A G 5: 33,184,349 (GRCm39) Y184C probably damaging Het
Zkscan16 C T 4: 58,946,125 (GRCm39) 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
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
R6197:Or10v9 UTSW 19 11,833,148 (GRCm39) missense probably damaging 0.99
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'- TACAAACAGAGTGGCCTCATG -3'
(R):5'- TGGCTAGCCTGGAGATCTTC -3'

Sequencing Primer
(F):5'- ACATGCCAGTCTCATGACAGGG -3'
(R):5'- GGCTAGCCTGGAGATCTTCTATTC -3'
Posted On 2015-04-17