Incidental Mutation 'R5876:Olfr8'
ID 455543
Institutional Source Beutler Lab
Gene Symbol Olfr8
Ensembl Gene ENSMUSG00000094080
Gene Name olfactory receptor 8
Synonyms MOR139-5P, GA_x6K02T2QGN0-2857086-2856154
Accession Numbers
Essential gene? Probably non essential (E-score: 0.136) question?
Stock # R5876 (G1)
Quality Score 225
Status Not validated
Chromosome 10
Chromosomal Location 78950636-78958378 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to T at 78955357 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 51 (I51F)
Ref Sequence ENSEMBL: ENSMUSP00000148856 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000081571] [ENSMUST00000203851] [ENSMUST00000214952]
AlphaFold Q60892
Predicted Effect probably benign
Transcript: ENSMUST00000081571
AA Change: I51F

PolyPhen 2 Score 0.147 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000080282
Gene: ENSMUSG00000094080
AA Change: I51F

DomainStartEndE-ValueType
Pfam:7tm_4 32 309 1.3e-47 PFAM
Pfam:7tm_1 42 291 3e-20 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000203851
AA Change: I51F

PolyPhen 2 Score 0.147 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000144916
Gene: ENSMUSG00000094080
AA Change: I51F

DomainStartEndE-ValueType
Pfam:7tm_4 32 309 1.3e-47 PFAM
Pfam:7tm_1 42 291 3e-20 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000214952
AA Change: I51F

PolyPhen 2 Score 0.147 (Sensitivity: 0.92; Specificity: 0.87)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000216819
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 97.9%
  • 20x: 93.6%
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: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700034E13Rik A G 18: 52,663,582 (GRCm38) D64G possibly damaging Het
Ano2 T A 6: 126,039,279 (GRCm38) M925K possibly damaging Het
Arnt2 T C 7: 84,347,512 (GRCm38) T69A probably damaging Het
Asap2 T A 12: 21,212,809 (GRCm38) N229K possibly damaging Het
Atp13a3 T A 16: 30,362,734 (GRCm38) N23Y probably benign Het
Cbr4 G A 8: 61,490,593 (GRCm38) G91R possibly damaging Het
Cdc27 A T 11: 104,515,418 (GRCm38) C624S probably benign Het
Cdc42bpg T A 19: 6,310,815 (GRCm38) I201N probably damaging Het
Cdh5 A G 8: 104,142,577 (GRCm38) Y645C probably damaging Het
Celsr2 C T 3: 108,413,943 (GRCm38) V518I probably damaging Het
Clca4b T C 3: 144,912,060 (GRCm38) T761A possibly damaging Het
Cpne4 C A 9: 104,925,770 (GRCm38) S204R probably damaging Het
Dcaf1 T C 9: 106,863,650 (GRCm38) W1279R probably damaging Het
Dennd4a C T 9: 64,911,755 (GRCm38) P1731S probably damaging Het
Dmxl1 T A 18: 49,870,984 (GRCm38) V892D possibly damaging Het
Fam131b A G 6: 42,321,248 (GRCm38) probably null Het
Fam83b T A 9: 76,491,850 (GRCm38) D657V possibly damaging Het
Fam83e T A 7: 45,722,363 (GRCm38) probably null Het
Fbxo4 A T 15: 3,977,819 (GRCm38) I121N probably damaging Het
Gabrg2 A G 11: 41,968,820 (GRCm38) S202P probably damaging Het
Gm10471 T C 5: 26,084,718 (GRCm38) E237G probably damaging Het
Grid2 T A 6: 64,663,162 (GRCm38) I788N probably damaging Het
Grik4 T A 9: 42,688,023 (GRCm38) N53Y probably damaging Het
Hipk2 A C 6: 38,730,867 (GRCm38) probably null Het
Hps5 T C 7: 46,789,196 (GRCm38) T38A probably damaging Het
Hs1bp3 A G 12: 8,341,843 (GRCm38) D315G possibly damaging Het
Kdm4a C T 4: 118,138,876 (GRCm38) M985I probably damaging Het
Kdm5d A G Y: 900,525 (GRCm38) Y190C probably damaging Het
Krt86 T C 15: 101,476,610 (GRCm38) S295P probably damaging Het
Matr3 T A 18: 35,587,738 (GRCm38) D413E probably benign Het
Mbd5 T A 2: 49,274,645 (GRCm38) F319L probably damaging Het
Mcoln1 T A 8: 3,510,910 (GRCm38) Y411N probably damaging Het
Mpdz C A 4: 81,285,474 (GRCm38) E1863* probably null Het
Mrps9 A G 1: 42,895,378 (GRCm38) E173G probably damaging Het
Osmr T C 15: 6,821,047 (GRCm38) T692A probably benign Het
Pkhd1l1 A T 15: 44,578,588 (GRCm38) H3641L possibly damaging Het
Pml T C 9: 58,233,182 (GRCm38) T421A possibly damaging Het
Podxl A G 6: 31,528,456 (GRCm38) probably null Het
Ppargc1b C G 18: 61,309,093 (GRCm38) D591H probably damaging Het
Prkag3 A G 1: 74,748,816 (GRCm38) probably benign Het
Proz A G 8: 13,073,448 (GRCm38) R240G probably benign Het
Ptpn13 C A 5: 103,476,960 (GRCm38) D43E probably damaging Het
Rbm5 T G 9: 107,760,326 (GRCm38) K135N probably damaging Het
Ska1 G A 18: 74,197,528 (GRCm38) T201M probably damaging Het
Slc35f5 A C 1: 125,587,363 (GRCm38) probably null Het
Slc9a3 T C 13: 74,161,723 (GRCm38) L510P probably damaging Het
Svil A G 18: 5,082,828 (GRCm38) K1231E probably damaging Het
Tanc2 T C 11: 105,922,613 (GRCm38) S1628P possibly damaging Het
Tm9sf3 T A 19: 41,240,584 (GRCm38) D260V probably damaging Het
Ttc9 G T 12: 81,631,622 (GRCm38) R73L probably damaging Het
Vps13b A G 15: 35,917,061 (GRCm38) I3684V probably damaging Het
Vps8 T C 16: 21,461,439 (GRCm38) probably null Het
Vwa3b T A 1: 37,076,439 (GRCm38) I328N probably damaging Het
Wdr1 C T 5: 38,530,023 (GRCm38) V222M probably benign Het
Xpnpep1 T A 19: 52,997,008 (GRCm38) T530S probably damaging Het
Zc3h6 C T 2: 128,993,277 (GRCm38) S111F probably benign Het
Zfp768 G A 7: 127,344,546 (GRCm38) P137S probably benign Het
Other mutations in Olfr8
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01022:Olfr8 APN 10 78,955,354 (GRCm38) missense possibly damaging 0.48
IGL01480:Olfr8 APN 10 78,956,144 (GRCm38) utr 3 prime probably benign
IGL02505:Olfr8 APN 10 78,955,933 (GRCm38) missense probably benign 0.02
IGL02543:Olfr8 APN 10 78,955,939 (GRCm38) missense probably damaging 1.00
IGL03323:Olfr8 APN 10 78,955,600 (GRCm38) missense probably benign
PIT4466001:Olfr8 UTSW 10 78,955,842 (GRCm38) missense probably benign 0.00
R1496:Olfr8 UTSW 10 78,955,848 (GRCm38) missense probably benign 0.41
R1754:Olfr8 UTSW 10 78,955,697 (GRCm38) missense probably damaging 0.99
R1878:Olfr8 UTSW 10 78,955,805 (GRCm38) missense possibly damaging 0.62
R2760:Olfr8 UTSW 10 78,956,042 (GRCm38) missense probably damaging 0.99
R4202:Olfr8 UTSW 10 78,955,295 (GRCm38) missense probably benign
R4206:Olfr8 UTSW 10 78,955,283 (GRCm38) missense probably benign 0.00
R4517:Olfr8 UTSW 10 78,956,043 (GRCm38) nonsense probably null
R4613:Olfr8 UTSW 10 78,956,065 (GRCm38) missense probably damaging 1.00
R4799:Olfr8 UTSW 10 78,956,097 (GRCm38) missense probably null 0.92
R4979:Olfr8 UTSW 10 78,955,932 (GRCm38) nonsense probably null
R5008:Olfr8 UTSW 10 78,956,071 (GRCm38) missense probably damaging 1.00
R5700:Olfr8 UTSW 10 78,955,484 (GRCm38) missense probably damaging 1.00
R6439:Olfr8 UTSW 10 78,955,984 (GRCm38) missense probably damaging 1.00
R6930:Olfr8 UTSW 10 78,955,781 (GRCm38) missense possibly damaging 0.84
R7110:Olfr8 UTSW 10 78,955,450 (GRCm38) missense possibly damaging 0.83
R7405:Olfr8 UTSW 10 78,955,697 (GRCm38) missense probably benign 0.14
R7524:Olfr8 UTSW 10 78,955,491 (GRCm38) nonsense probably null
R8198:Olfr8 UTSW 10 78,955,724 (GRCm38) missense probably damaging 0.97
R9227:Olfr8 UTSW 10 78,956,095 (GRCm38) missense possibly damaging 0.92
R9230:Olfr8 UTSW 10 78,956,095 (GRCm38) missense possibly damaging 0.92
Z1176:Olfr8 UTSW 10 78,955,219 (GRCm38) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TCTCATAGACACATGTGACTGATG -3'
(R):5'- TAGCCACATATCGGTCATAGGCC -3'

Sequencing Primer
(F):5'- CATAGACACATGTGACTGATGGAATC -3'
(R):5'- CCAGGAGAAAGTTGTCCAATTCTGC -3'
Posted On 2017-02-10