Incidental Mutation 'R2238:Or10v5'
ID 240270
Institutional Source Beutler Lab
Gene Symbol Or10v5
Ensembl Gene ENSMUSG00000048292
Gene Name olfactory receptor family 10 subfamily V member 5
Synonyms MOR266-2, GA_x6K02T2RE5P-2172809-2171862, Olfr1417
MMRRC Submission 040238-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.073) question?
Stock # R2238 (G1)
Quality Score 225
Status Validated
Chromosome 19
Chromosomal Location 11805441-11806388 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 11805814 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 192 (D192G)
Ref Sequence ENSEMBL: ENSMUSP00000149141 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000061235] [ENSMUST00000214887]
AlphaFold Q8VGJ6
Predicted Effect probably damaging
Transcript: ENSMUST00000061235
AA Change: D192G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000062542
Gene: ENSMUSG00000048292
AA Change: D192G

DomainStartEndE-ValueType
Pfam:7tm_4 31 309 3.3e-53 PFAM
Pfam:7tm_1 41 291 3.1e-22 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000213141
Predicted Effect probably damaging
Transcript: ENSMUST00000214887
AA Change: D192G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Meta Mutation Damage Score 0.2045 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.0%
Validation Efficiency 98% (59/60)
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: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl4fm1 T A 4: 144,246,469 (GRCm39) V5E possibly damaging Het
Acaca T C 11: 84,282,331 (GRCm39) probably benign Het
Adam18 T C 8: 25,136,303 (GRCm39) E406G probably benign Het
Adgrl4 A T 3: 151,205,779 (GRCm39) I164F probably damaging Het
Arhgap36 G T X: 48,582,282 (GRCm39) V60L possibly damaging Het
Bmi1 T C 2: 18,688,225 (GRCm39) probably benign Het
Carf T C 1: 60,187,193 (GRCm39) S599P probably benign Het
Cdc37 G A 9: 21,053,829 (GRCm39) Q176* probably null Het
Clca3a1 T A 3: 144,457,766 (GRCm39) I373F possibly damaging Het
Clnk A G 5: 38,921,694 (GRCm39) probably benign Het
Cnot1 T C 8: 96,496,149 (GRCm39) I342V probably benign Het
Dact2 A T 17: 14,417,312 (GRCm39) L296Q probably damaging Het
Dctn2 C T 10: 127,112,257 (GRCm39) T123I probably damaging Het
Deup1 A C 9: 15,486,597 (GRCm39) I455S probably damaging Het
Dnmbp A G 19: 43,857,303 (GRCm39) V957A possibly damaging Het
Emilin2 T C 17: 71,581,734 (GRCm39) R331G possibly damaging Het
Eomes A G 9: 118,311,359 (GRCm39) D394G probably damaging Het
Epn1 A G 7: 5,100,601 (GRCm39) N518S probably damaging Het
Gbf1 T C 19: 46,152,057 (GRCm39) I30T probably benign Het
Gcc1 A G 6: 28,420,462 (GRCm39) V285A probably benign Het
Gopc T C 10: 52,229,499 (GRCm39) H188R probably damaging Het
Herc6 A G 6: 57,631,386 (GRCm39) N693D probably benign Het
Hipk2 A G 6: 38,706,850 (GRCm39) probably benign Het
Htatsf1 G T X: 56,111,864 (GRCm39) D642Y unknown Het
Ints1 G A 5: 139,750,955 (GRCm39) T814M possibly damaging Het
Kdm6a T C X: 18,065,476 (GRCm39) F104S probably damaging Het
Kdr T A 5: 76,110,179 (GRCm39) Y936F possibly damaging Het
Ly6k T C 15: 74,669,018 (GRCm39) E87G probably benign Het
Lyst A G 13: 13,917,848 (GRCm39) N3303D probably benign Het
Mindy4 T C 6: 55,278,055 (GRCm39) F633S probably damaging Het
Msl2 T A 9: 100,978,569 (GRCm39) N314K probably benign Het
Ncapd3 A G 9: 26,978,320 (GRCm39) T840A probably benign Het
Neil3 T C 8: 54,052,311 (GRCm39) D429G possibly damaging Het
Nt5c1b C A 12: 10,425,558 (GRCm39) T309K probably damaging Het
Nt5c1b A G 12: 10,440,108 (GRCm39) Y550C probably damaging Het
Pabpc4l A C 3: 46,401,137 (GRCm39) V169G probably damaging Het
Pcgf5 A T 19: 36,414,754 (GRCm39) N105I probably damaging Het
Phka2 A G X: 159,324,408 (GRCm39) E254G probably damaging Het
Pik3cb A G 9: 98,923,081 (GRCm39) Y984H probably damaging Het
Ptprz1 A T 6: 22,987,376 (GRCm39) Q387L probably damaging Het
Rassf8 T C 6: 145,762,910 (GRCm39) V419A probably damaging Het
Rnf148 T C 6: 23,654,345 (GRCm39) Y217C probably benign Het
Sec24d T A 3: 123,143,543 (GRCm39) probably null Het
Sesn3 T C 9: 14,219,761 (GRCm39) V50A probably benign Het
Sgcd T C 11: 47,023,509 (GRCm39) N99D possibly damaging Het
Sncaip T C 18: 53,001,619 (GRCm39) S47P probably damaging Het
Sp2 C T 11: 96,846,762 (GRCm39) C527Y probably damaging Het
Spata4 A C 8: 55,055,664 (GRCm39) K185T probably benign Het
Spin2c A G X: 152,616,672 (GRCm39) I162V probably damaging Het
Srcin1 T C 11: 97,425,645 (GRCm39) T471A probably benign Het
Stac G A 9: 111,519,190 (GRCm39) probably benign Het
Tcaf3 A G 6: 42,570,262 (GRCm39) Y497H probably benign Het
Tmem40 C T 6: 115,708,038 (GRCm39) W150* probably null Het
Tmem59l T C 8: 70,937,772 (GRCm39) T203A probably damaging Het
Tnfsf11 A T 14: 78,537,421 (GRCm39) S81T possibly damaging Het
Topaz1 C T 9: 122,600,212 (GRCm39) T984I probably benign Het
Vmn1r204 A G 13: 22,740,993 (GRCm39) H208R probably benign Het
Vmn2r98 T A 17: 19,286,213 (GRCm39) M237K probably damaging Het
Other mutations in Or10v5
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0530:Or10v5 UTSW 19 11,805,556 (GRCm39) missense probably benign 0.26
R1532:Or10v5 UTSW 19 11,805,983 (GRCm39) missense probably benign 0.00
R1730:Or10v5 UTSW 19 11,805,445 (GRCm39) missense probably benign 0.06
R2032:Or10v5 UTSW 19 11,805,664 (GRCm39) missense probably damaging 1.00
R2237:Or10v5 UTSW 19 11,805,814 (GRCm39) missense probably damaging 1.00
R2239:Or10v5 UTSW 19 11,805,814 (GRCm39) missense probably damaging 1.00
R4959:Or10v5 UTSW 19 11,806,300 (GRCm39) missense probably benign
R4973:Or10v5 UTSW 19 11,806,300 (GRCm39) missense probably benign
R5015:Or10v5 UTSW 19 11,805,482 (GRCm39) missense probably benign 0.00
R6799:Or10v5 UTSW 19 11,806,178 (GRCm39) missense possibly damaging 0.91
R6984:Or10v5 UTSW 19 11,805,668 (GRCm39) missense probably damaging 1.00
R7063:Or10v5 UTSW 19 11,805,548 (GRCm39) missense probably damaging 1.00
R7222:Or10v5 UTSW 19 11,806,021 (GRCm39) missense probably damaging 0.99
R8021:Or10v5 UTSW 19 11,806,256 (GRCm39) missense probably benign 0.39
R8748:Or10v5 UTSW 19 11,805,596 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CATACTGCAGGAGGACAACG -3'
(R):5'- TATGACCGGTTTGTGGCCATC -3'

Sequencing Primer
(F):5'- CTGCAGGAGGACAACGGTCAG -3'
(R):5'- GCGCTATACCCTCATCATGAG -3'
Posted On 2014-10-15