Incidental Mutation 'IGL03073:Olfr1466'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Olfr1466
Ensembl Gene ENSMUSG00000096485
Gene Nameolfactory receptor 1466
SynonymsMOR202-12, GA_x6K02T2RE5P-3672907-3673839
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.086) question?
Stock #IGL03073
Quality Score
Chromosomal Location13338862-13343572 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to G at 13342022 bp
Amino Acid Change Isoleucine to Arginine at position 88 (I88R)
Ref Sequence ENSEMBL: ENSMUSP00000147188 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000075868] [ENSMUST00000207124]
Predicted Effect probably benign
Transcript: ENSMUST00000075868
AA Change: I88R

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000075265
Gene: ENSMUSG00000096485
AA Change: I88R

Pfam:7tm_4 32 310 4.1e-49 PFAM
Pfam:7TM_GPCR_Srsx 36 306 1.9e-6 PFAM
Pfam:7tm_1 42 291 7e-19 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000207124
AA Change: I88R

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
Coding Region Coverage
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: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930504O13Rik A T 11: 58,447,451 D38E probably damaging Het
4933440M02Rik T C 7: 125,331,563 noncoding transcript Het
Actr6 A G 10: 89,726,694 S108P probably damaging Het
Adam34 A T 8: 43,650,903 N568K probably damaging Het
Anpep A G 7: 79,838,955 L408P probably damaging Het
Atp13a1 T C 8: 69,798,502 V459A probably damaging Het
Atp2b1 C T 10: 98,999,851 T486M probably damaging Het
Cdc42bpa T A 1: 180,094,376 probably benign Het
Espnl T C 1: 91,344,556 I502T probably damaging Het
Fancm T C 12: 65,101,632 Y674H probably damaging Het
Gnaq T A 19: 16,316,106 N137K probably benign Het
Igf1r T A 7: 68,215,043 D1196E probably damaging Het
Insrr A G 3: 87,809,938 probably benign Het
Mcf2l C A 8: 13,000,004 H313N probably damaging Het
Mdh1b C T 1: 63,721,487 probably null Het
Mrc1 G A 2: 14,305,342 V805I probably damaging Het
Ncam2 T G 16: 81,621,347 D763E possibly damaging Het
Ncapg2 T G 12: 116,452,274 H1091Q probably benign Het
Olfr1098 A G 2: 86,923,353 Y60H probably damaging Het
Pcdh18 T A 3: 49,753,367 D886V possibly damaging Het
Pdlim4 A G 11: 54,063,641 V21A probably damaging Het
Safb2 A G 17: 56,571,289 S24P probably benign Het
Sec16a A G 2: 26,439,183 M940T probably benign Het
Snx14 A G 9: 88,422,896 probably null Het
Sox1 T C 8: 12,396,625 W89R probably damaging Het
Stx12 T C 4: 132,858,449 M207V probably benign Het
Tex14 A G 11: 87,535,609 T1154A probably damaging Het
Tmcc3 T G 10: 94,578,951 S172A probably benign Het
Tnc T A 4: 63,971,224 I1773F possibly damaging Het
Tshz3 A T 7: 36,770,745 N720Y probably damaging Het
Usp19 G A 9: 108,495,803 probably benign Het
Vmn1r170 A C 7: 23,606,848 Q225P probably damaging Het
Vmn2r89 A G 14: 51,456,071 I293V possibly damaging Het
Other mutations in Olfr1466
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02442:Olfr1466 APN 19 13342120 missense probably benign 0.13
IGL02568:Olfr1466 APN 19 13342219 missense probably benign 0.08
R0943:Olfr1466 UTSW 19 13341793 missense probably benign 0.00
R1301:Olfr1466 UTSW 19 13341847 missense probably benign 0.05
R1355:Olfr1466 UTSW 19 13342518 nonsense probably null
R1524:Olfr1466 UTSW 19 13342122 nonsense probably null
R1568:Olfr1466 UTSW 19 13342175 missense probably benign 0.14
R1993:Olfr1466 UTSW 19 13341814 missense possibly damaging 0.65
R2031:Olfr1466 UTSW 19 13342406 missense probably benign 0.18
R3693:Olfr1466 UTSW 19 13342529 missense possibly damaging 0.73
R3694:Olfr1466 UTSW 19 13342529 missense possibly damaging 0.73
R3853:Olfr1466 UTSW 19 13342498 missense possibly damaging 0.55
R5313:Olfr1466 UTSW 19 13342065 missense probably benign 0.07
R5467:Olfr1466 UTSW 19 13342157 missense probably damaging 1.00
R6060:Olfr1466 UTSW 19 13342133 missense probably benign 0.08
R7125:Olfr1466 UTSW 19 13341739 critical splice acceptor site probably null
R7591:Olfr1466 UTSW 19 13342255 missense probably benign 0.28
Z1177:Olfr1466 UTSW 19 13342255 missense probably benign 0.28
Posted On2016-08-02