Incidental Mutation 'R0940:Or5p66'
ID 81408
Institutional Source Beutler Lab
Gene Symbol Or5p66
Ensembl Gene ENSMUSG00000109884
Gene Name olfactory receptor family 5 subfamily P member 66
Synonyms Olfr490, GA_x6K02T2PBJ9-10617173-10616229, MOR204-17
MMRRC Submission 039079-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.160) question?
Stock # R0940 (G1)
Quality Score 225
Status Validated
Chromosome 7
Chromosomal Location 107885387-107886331 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 107886264 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 23 (D23G)
Ref Sequence ENSEMBL: ENSMUSP00000147922 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000210114] [ENSMUST00000211345]
AlphaFold Q8VFD2
Predicted Effect probably benign
Transcript: ENSMUST00000074550
AA Change: D23G

PolyPhen 2 Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000074137
Gene: ENSMUSG00000093808
AA Change: D23G

DomainStartEndE-ValueType
Pfam:7tm_4 34 311 4e-53 PFAM
Pfam:7tm_1 44 293 5e-23 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000210114
AA Change: D23G

PolyPhen 2 Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)
Predicted Effect probably benign
Transcript: ENSMUST00000211345
AA Change: D23G

PolyPhen 2 Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)
Meta Mutation Damage Score 0.4804 question?
Coding Region Coverage
  • 1x: 99.5%
  • 3x: 99.1%
  • 10x: 98.0%
  • 20x: 96.7%
Validation Efficiency 100% (68/68)
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: 63 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1810064F22Rik C T 9: 22,119,367 (GRCm39) noncoding transcript Het
2610021A01Rik T G 7: 41,275,858 (GRCm39) I520M probably damaging Het
Ackr4 A G 9: 103,976,831 (GRCm39) F39L probably damaging Het
Adgre5 C T 8: 84,460,126 (GRCm39) S92N probably damaging Het
Adrb2 T C 18: 62,312,762 (GRCm39) D21G probably benign Het
Akr1c6 G A 13: 4,486,372 (GRCm39) E60K probably benign Het
Bcl7c T A 7: 127,306,503 (GRCm39) N96I possibly damaging Het
Brca1 A T 11: 101,422,969 (GRCm39) S106R possibly damaging Het
C6 A T 15: 4,764,717 (GRCm39) T138S probably benign Het
Cul3 T C 1: 80,300,564 (GRCm39) probably benign Het
Dnah8 T A 17: 31,022,217 (GRCm39) M3939K probably damaging Het
Dock4 T A 12: 40,681,626 (GRCm39) probably benign Het
Dsc2 T G 18: 20,183,116 (GRCm39) T101P probably damaging Het
Dynlt1b T C 17: 6,697,649 (GRCm39) probably benign Het
E330013P04Rik A G 19: 60,150,354 (GRCm39) noncoding transcript Het
Fggy A G 4: 95,585,238 (GRCm39) E39G probably benign Het
Fhip1a A G 3: 85,572,797 (GRCm39) V952A possibly damaging Het
Fmo6 A T 1: 162,753,795 (GRCm39) C116S probably benign Het
Gadd45a A G 6: 67,013,813 (GRCm39) I44T possibly damaging Het
Gmps A G 3: 63,883,743 (GRCm39) probably benign Het
Gnmt A G 17: 47,037,271 (GRCm39) L171P probably damaging Het
Hnrnpm G A 17: 33,868,976 (GRCm39) R523C probably damaging Het
Inpp5a T C 7: 139,105,654 (GRCm39) Y202H probably damaging Het
Kank3 C T 17: 34,036,450 (GRCm39) S106F probably damaging Het
Lmcd1 A G 6: 112,305,658 (GRCm39) D253G probably benign Het
Lrrk2 A T 15: 91,613,284 (GRCm39) I803F possibly damaging Het
Mybpc2 T C 7: 44,156,311 (GRCm39) K834R probably benign Het
Mycbp2 A T 14: 103,500,129 (GRCm39) probably benign Het
Myh4 A T 11: 67,133,689 (GRCm39) N243Y probably damaging Het
Myorg A G 4: 41,497,996 (GRCm39) Y545H probably damaging Het
Nfatc1 C T 18: 80,679,110 (GRCm39) M759I probably benign Het
Nipal4 A G 11: 46,041,139 (GRCm39) I352T possibly damaging Het
Nomo1 A G 7: 45,683,329 (GRCm39) E25G possibly damaging Het
Or10j27 A G 1: 172,958,020 (GRCm39) S255P probably benign Het
Or13a19 T C 7: 139,903,065 (GRCm39) I151T probably benign Het
Or14j7 A G 17: 38,234,591 (GRCm39) I45V probably damaging Het
Or1e32 T C 11: 73,705,050 (GRCm39) N286S probably damaging Het
Or4c116 T A 2: 88,942,419 (GRCm39) I146L probably benign Het
Pabpn1l A G 8: 123,349,183 (GRCm39) V78A probably benign Het
Pde6b T A 5: 108,568,203 (GRCm39) I327N possibly damaging Het
Phrf1 T C 7: 140,834,768 (GRCm39) probably benign Het
Pkm C T 9: 59,575,818 (GRCm39) probably benign Het
Plxna2 G A 1: 194,482,863 (GRCm39) V1519I probably benign Het
Ppp2cb T C 8: 34,105,689 (GRCm39) probably null Het
Prickle2 A G 6: 92,387,984 (GRCm39) Y473H probably benign Het
Prpf3 A G 3: 95,751,535 (GRCm39) W389R probably damaging Het
Psme4 G A 11: 30,765,264 (GRCm39) E544K possibly damaging Het
Relb A T 7: 19,345,767 (GRCm39) D395E probably damaging Het
Rif1 GCCACCA GCCA 2: 52,000,336 (GRCm39) probably benign Het
Rnf213 A G 11: 119,307,389 (GRCm39) N683S probably benign Het
Rtel1 T C 2: 180,964,596 (GRCm39) C102R probably benign Het
Sel1l3 C T 5: 53,301,379 (GRCm39) probably benign Het
Slc8a2 A G 7: 15,878,887 (GRCm39) T458A probably benign Het
Smc3 T A 19: 53,629,340 (GRCm39) M931K probably benign Het
Sorbs2 T C 8: 46,249,539 (GRCm39) V795A probably benign Het
Tgm3 A G 2: 129,854,326 (GRCm39) S2G probably benign Het
Tpbpa T C 13: 61,087,867 (GRCm39) T75A probably damaging Het
Trub1 A G 19: 57,473,495 (GRCm39) probably benign Het
Uggt2 A G 14: 119,328,604 (GRCm39) probably null Het
Ugt2a3 A G 5: 87,475,065 (GRCm39) V393A possibly damaging Het
Vav3 T A 3: 109,470,151 (GRCm39) M532K possibly damaging Het
Zfp616 A T 11: 73,975,850 (GRCm39) K706N probably damaging Het
Zkscan1 T C 5: 138,091,432 (GRCm39) F55S probably damaging Het
Other mutations in Or5p66
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0395:Or5p66 UTSW 7 107,885,478 (GRCm39) missense probably benign 0.00
R0634:Or5p66 UTSW 7 107,885,503 (GRCm39) missense probably benign 0.00
R1990:Or5p66 UTSW 7 107,885,566 (GRCm39) nonsense probably null
R1991:Or5p66 UTSW 7 107,885,566 (GRCm39) nonsense probably null
R2860:Or5p66 UTSW 7 107,886,169 (GRCm39) missense probably damaging 0.98
R2861:Or5p66 UTSW 7 107,886,169 (GRCm39) missense probably damaging 0.98
R3712:Or5p66 UTSW 7 107,885,663 (GRCm39) nonsense probably null
R4735:Or5p66 UTSW 7 107,885,520 (GRCm39) missense probably benign
R4895:Or5p66 UTSW 7 107,885,802 (GRCm39) missense probably damaging 0.97
R4976:Or5p66 UTSW 7 107,885,818 (GRCm39) missense probably damaging 1.00
R5686:Or5p66 UTSW 7 107,885,949 (GRCm39) missense probably damaging 1.00
R5719:Or5p66 UTSW 7 107,885,599 (GRCm39) missense probably damaging 0.97
R5883:Or5p66 UTSW 7 107,885,451 (GRCm39) missense probably damaging 1.00
R5911:Or5p66 UTSW 7 107,885,605 (GRCm39) missense probably damaging 1.00
R6452:Or5p66 UTSW 7 107,886,100 (GRCm39) missense probably damaging 1.00
R7018:Or5p66 UTSW 7 107,885,551 (GRCm39) missense probably benign 0.34
R7233:Or5p66 UTSW 7 107,885,923 (GRCm39) missense probably benign 0.36
R8085:Or5p66 UTSW 7 107,885,620 (GRCm39) missense probably benign 0.01
R8166:Or5p66 UTSW 7 107,885,904 (GRCm39) missense probably benign 0.06
R8919:Or5p66 UTSW 7 107,886,289 (GRCm39) missense probably damaging 1.00
R9209:Or5p66 UTSW 7 107,885,526 (GRCm39) missense probably benign 0.06
R9612:Or5p66 UTSW 7 107,885,487 (GRCm39) missense probably benign
R9789:Or5p66 UTSW 7 107,885,898 (GRCm39) missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- GTCCACagaagagaagagaaaagaaggaaa -3'
(R):5'- ATCCAATCTAGCACCCCAATTACATGTTT -3'

Sequencing Primer
(F):5'- agaaaagaaggaaagtaaaaaggagg -3'
(R):5'- GCACCCCAATTACATGTTTTAAATG -3'
Posted On 2013-11-07