Incidental Mutation 'R9187:Olfr855'
ID 697451
Institutional Source Beutler Lab
Gene Symbol Olfr855
Ensembl Gene ENSMUSG00000043087
Gene Name olfactory receptor 855
Synonyms MOR148-1, GA_x6K02T2PVTD-13330461-13331399
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.147) question?
Stock # R9187 (G1)
Quality Score 225.009
Status Validated
Chromosome 9
Chromosomal Location 19582617-19586030 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to C at 19584654 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Threonine at position 39 (I39T)
Ref Sequence ENSEMBL: ENSMUSP00000150218 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000061693] [ENSMUST00000215587]
AlphaFold Q7TRF8
Predicted Effect probably benign
Transcript: ENSMUST00000061693
AA Change: I39T

PolyPhen 2 Score 0.033 (Sensitivity: 0.95; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000054790
Gene: ENSMUSG00000043087
AA Change: I39T

DomainStartEndE-ValueType
Pfam:7tm_4 33 310 1.7e-54 PFAM
Pfam:7TM_GPCR_Srsx 37 182 5.2e-8 PFAM
Pfam:7tm_1 43 292 2.5e-24 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000215587
AA Change: I39T

PolyPhen 2 Score 0.033 (Sensitivity: 0.95; Specificity: 0.82)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.5%
Validation Efficiency 97% (70/72)
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: 75 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca5 A G 11: 110,310,135 (GRCm38) probably null Het
Abcb1a T A 5: 8,715,016 (GRCm38) C669S probably benign Het
Abcc3 A G 11: 94,365,087 (GRCm38) L524P probably damaging Het
Akap5 A T 12: 76,329,971 (GRCm38) K726* probably null Het
Aldh16a1 T C 7: 45,142,017 (GRCm38) E778G probably damaging Het
Ankle2 G A 5: 110,252,744 (GRCm38) V649M possibly damaging Het
Apon A G 10: 128,254,963 (GRCm38) N170S probably benign Het
Baiap2l1 T C 5: 144,280,954 (GRCm38) Y274C probably benign Het
Bub1 A T 2: 127,814,936 (GRCm38) N425K possibly damaging Het
Camsap1 A G 2: 25,930,016 (GRCm38) C1487R probably damaging Het
Cd4 A C 6: 124,867,688 (GRCm38) V378G probably damaging Het
Cenpa C A 5: 30,667,036 (GRCm38) P3Q unknown Het
Cfap44 T C 16: 44,404,781 (GRCm38) probably benign Het
Cfap65 T A 1: 74,917,358 (GRCm38) M1021L probably benign Het
Ddx39 G T 8: 83,722,484 (GRCm38) M300I probably benign Het
Dgkh T C 14: 78,595,161 (GRCm38) R819G probably damaging Het
Dlc1 A T 8: 36,938,632 (GRCm38) M1K probably null Het
Dnah9 A G 11: 66,005,146 (GRCm38) W2468R probably benign Het
Ebag9 A T 15: 44,640,310 (GRCm38) K177I probably damaging Het
Ehbp1 T C 11: 22,151,184 (GRCm38) I249V probably damaging Het
Fam171b T C 2: 83,880,021 (GRCm38) V679A probably damaging Het
Gabbr2 G A 4: 46,674,533 (GRCm38) T818I probably damaging Het
Gcn1l1 T C 5: 115,614,118 (GRCm38) S2098P probably damaging Het
Glb1 T C 9: 114,473,923 (GRCm38) I609T probably damaging Het
Gm12355 A G 11: 98,625,361 (GRCm38) V62A possibly damaging Het
Gm5916 T G 9: 36,120,724 (GRCm38) H88P probably benign Het
Gm6205 T C 5: 94,683,896 (GRCm38) V254A probably benign Het
Gon4l T C 3: 88,879,311 (GRCm38) S586P probably benign Het
Gzmg T A 14: 56,157,257 (GRCm38) T185S probably benign Het
Hipk3 T A 2: 104,446,591 (GRCm38) D381V probably damaging Het
Hnrnpul2 C A 19: 8,830,955 (GRCm38) N681K probably benign Het
Hpdl C A 4: 116,821,175 (GRCm38) G30C probably damaging Het
Iws1 G A 18: 32,080,160 (GRCm38) E214K possibly damaging Het
Krt82 C A 15: 101,541,825 (GRCm38) V479L probably benign Het
Lama4 G A 10: 39,048,128 (GRCm38) probably null Het
Lamc1 C A 1: 153,221,688 (GRCm38) E1537* probably null Het
Mab21l3 G A 3: 101,823,278 (GRCm38) T215M probably benign Het
Magi3 C A 3: 104,015,757 (GRCm38) V1215F possibly damaging Het
Mical2 T A 7: 112,303,590 (GRCm38) C89* probably null Het
Mitf T A 6: 98,017,874 (GRCm38) V427D probably benign Het
Muc4 T C 16: 32,768,728 (GRCm38) V753A Het
Myo16 G A 8: 10,442,233 (GRCm38) R725H unknown Het
Ncapg2 T A 12: 116,438,667 (GRCm38) D706E probably damaging Het
Ndst1 T C 18: 60,691,196 (GRCm38) D803G probably benign Het
Neb A T 2: 52,206,103 (GRCm38) V5065D probably damaging Het
Npm3 G A 19: 45,749,502 (GRCm38) R19* probably null Het
Ntrk3 A C 7: 78,247,218 (GRCm38) N690K possibly damaging Het
Olfr850 T C 9: 19,477,870 (GRCm38) I127V probably benign Het
Olfr985 C A 9: 40,127,590 (GRCm38) V124L possibly damaging Het
P3h2 G A 16: 26,105,436 (GRCm38) A83V probably benign Het
Pdia2 A G 17: 26,196,936 (GRCm38) S362P probably damaging Het
Pmp22 T C 11: 63,134,491 (GRCm38) V50A probably benign Het
Pmp22 C T 11: 63,134,442 (GRCm38) H34Y probably benign Het
Ppfia4 T C 1: 134,327,268 (GRCm38) D283G probably damaging Het
Prss55 T A 14: 64,077,082 (GRCm38) Q213L probably null Het
Rgsl1 C T 1: 153,793,867 (GRCm38) E258K possibly damaging Het
Ripor2 T C 13: 24,713,649 (GRCm38) F777L probably benign Het
Rsf1 GGC GGCGGCGGCCGC 7: 97,579,933 (GRCm38) probably benign Het
Sgce G A 6: 4,711,362 (GRCm38) R173C probably benign Het
Sncaip T G 18: 52,906,939 (GRCm38) M735R probably benign Het
Snrpd2 T A 7: 19,152,580 (GRCm38) I96N probably damaging Het
Spryd3 T G 15: 102,130,675 (GRCm38) D121A probably damaging Het
Sspo T C 6: 48,495,289 (GRCm38) C149R probably damaging Het
Tbc1d10b A T 7: 127,207,933 (GRCm38) M144K probably benign Het
Tbc1d31 T A 15: 57,916,089 (GRCm38) I66N probably damaging Het
Tssk1 A G 16: 17,894,593 (GRCm38) T81A possibly damaging Het
Ttc28 A G 5: 111,102,036 (GRCm38) Y284C probably damaging Het
Ttn T C 2: 76,743,411 (GRCm38) T25713A probably benign Het
Vmn2r125 T C 4: 156,351,259 (GRCm38) W311R probably damaging Het
Vmn2r80 A T 10: 79,194,604 (GRCm38) T755S probably benign Het
Vmn2r98 T C 17: 19,081,219 (GRCm38) C828R probably damaging Het
Wwox T C 8: 114,712,238 (GRCm38) F348S probably damaging Het
Zeb2 T A 2: 45,110,028 (GRCm38) R65W possibly damaging Het
Zfp712 T A 13: 67,040,573 (GRCm38) H630L probably damaging Het
Zfp764 G T 7: 127,405,436 (GRCm38) H174Q probably damaging Het
Other mutations in Olfr855
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01020:Olfr855 APN 9 19,585,320 (GRCm38) missense possibly damaging 0.74
IGL01405:Olfr855 APN 9 19,585,205 (GRCm38) missense probably benign 0.23
IGL01775:Olfr855 APN 9 19,584,705 (GRCm38) missense probably benign 0.04
IGL01920:Olfr855 APN 9 19,585,022 (GRCm38) missense probably benign 0.01
R0501:Olfr855 UTSW 9 19,584,618 (GRCm38) missense probably damaging 1.00
R0600:Olfr855 UTSW 9 19,585,304 (GRCm38) missense possibly damaging 0.47
R0667:Olfr855 UTSW 9 19,585,447 (GRCm38) missense probably benign
R1769:Olfr855 UTSW 9 19,585,386 (GRCm38) missense probably damaging 0.98
R3117:Olfr855 UTSW 9 19,584,941 (GRCm38) missense probably damaging 0.99
R4002:Olfr855 UTSW 9 19,584,714 (GRCm38) missense probably damaging 1.00
R4003:Olfr855 UTSW 9 19,584,714 (GRCm38) missense probably damaging 1.00
R4043:Olfr855 UTSW 9 19,584,995 (GRCm38) missense probably benign 0.16
R4243:Olfr855 UTSW 9 19,584,558 (GRCm38) missense probably damaging 1.00
R4672:Olfr855 UTSW 9 19,585,430 (GRCm38) missense possibly damaging 0.74
R4673:Olfr855 UTSW 9 19,585,430 (GRCm38) missense possibly damaging 0.74
R4959:Olfr855 UTSW 9 19,585,208 (GRCm38) missense probably benign
R4973:Olfr855 UTSW 9 19,585,208 (GRCm38) missense probably benign
R5223:Olfr855 UTSW 9 19,585,026 (GRCm38) missense probably benign 0.16
R5681:Olfr855 UTSW 9 19,584,899 (GRCm38) missense probably damaging 1.00
R6005:Olfr855 UTSW 9 19,584,885 (GRCm38) missense probably benign 0.45
R6017:Olfr855 UTSW 9 19,585,434 (GRCm38) missense probably benign 0.00
R6145:Olfr855 UTSW 9 19,584,888 (GRCm38) missense probably benign 0.02
R6615:Olfr855 UTSW 9 19,584,989 (GRCm38) missense probably benign 0.05
R6771:Olfr855 UTSW 9 19,585,379 (GRCm38) missense probably benign 0.16
R6969:Olfr855 UTSW 9 19,584,590 (GRCm38) missense possibly damaging 0.77
R7239:Olfr855 UTSW 9 19,585,191 (GRCm38) missense probably damaging 1.00
R7313:Olfr855 UTSW 9 19,584,642 (GRCm38) missense probably damaging 1.00
R7361:Olfr855 UTSW 9 19,584,560 (GRCm38) missense probably benign 0.00
R8112:Olfr855 UTSW 9 19,584,724 (GRCm38) missense probably benign 0.44
R8470:Olfr855 UTSW 9 19,584,969 (GRCm38) missense probably damaging 0.99
R9155:Olfr855 UTSW 9 19,585,083 (GRCm38) missense probably benign 0.00
R9422:Olfr855 UTSW 9 19,584,672 (GRCm38) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- ACTTGAGCATGGCATGGAAG -3'
(R):5'- GCAGTCTGTGTAAGTGATGCTC -3'

Sequencing Primer
(F):5'- CTTGAGCATGGCATGGAAGTAGTTAG -3'
(R):5'- AAGTGATGCTCTGGTCATTTGC -3'
Posted On 2022-02-07