Incidental Mutation 'R1521:Olfr872'
ID 167001
Institutional Source Beutler Lab
Gene Symbol Olfr872
Ensembl Gene ENSMUSG00000066897
Gene Name olfactory receptor 872
Synonyms GA_x6K02T2PVTD-13999915-14000844, MOR145-3
MMRRC Submission 040870-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.060) question?
Stock # R1521 (G1)
Quality Score 225
Status Not validated
Chromosome 9
Chromosomal Location 20237119-20261643 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to C at 20260432 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Glutamine to Histidine at position 197 (Q197H)
Ref Sequence ENSEMBL: ENSMUSP00000083665 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000086474]
AlphaFold E9PVW2
Predicted Effect possibly damaging
Transcript: ENSMUST00000086474
AA Change: Q197H

PolyPhen 2 Score 0.912 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000083665
Gene: ENSMUSG00000066897
AA Change: Q197H

Pfam:7tm_4 45 321 3.8e-45 PFAM
Pfam:7TM_GPCR_Srsx 49 310 1.4e-9 PFAM
Pfam:7tm_1 55 304 4.2e-21 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000212245
Predicted Effect noncoding transcript
Transcript: ENSMUST00000212574
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.8%
  • 20x: 94.6%
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: 118 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adat1 A G 8: 111,987,235 (GRCm38) L104P possibly damaging Het
Adgrf5 T C 17: 43,430,552 (GRCm38) V360A probably benign Het
Ahnak G A 19: 9,004,728 (GRCm38) M1125I probably benign Het
Akap12 T C 10: 4,354,804 (GRCm38) V538A probably benign Het
Arhgef10l T C 4: 140,515,438 (GRCm38) D1088G possibly damaging Het
Atp7b A T 8: 22,027,673 (GRCm38) L268Q probably damaging Het
Atxn2 A C 5: 121,779,591 (GRCm38) N516T probably damaging Het
Cacna1h T C 17: 25,397,354 (GRCm38) M184V possibly damaging Het
Cacnb2 G T 2: 14,614,352 (GRCm38) R66L probably benign Het
Casp8ap2 A G 4: 32,631,867 (GRCm38) E96G probably damaging Het
Ccdc78 G T 17: 25,788,781 (GRCm38) R264L probably damaging Het
Cdh4 G A 2: 179,797,558 (GRCm38) R166H probably damaging Het
Cog7 C T 7: 121,930,574 (GRCm38) D615N possibly damaging Het
Crtc2 T C 3: 90,257,383 (GRCm38) V115A probably benign Het
Crybg1 A G 10: 43,998,416 (GRCm38) S899P probably damaging Het
Ctdnep1 T A 11: 69,988,635 (GRCm38) V128E probably damaging Het
Ctnna3 A G 10: 64,959,842 (GRCm38) K780E probably benign Het
Cul7 T A 17: 46,663,190 (GRCm38) L1467H probably damaging Het
Dazap2 T A 15: 100,618,065 (GRCm38) Y91* probably null Het
Dcdc5 T C 2: 106,351,669 (GRCm38) noncoding transcript Het
Dppa1 T A 11: 46,610,473 (GRCm38) R74S possibly damaging Het
Elovl1 A T 4: 118,432,000 (GRCm38) T241S probably benign Het
Eya1 G T 1: 14,274,550 (GRCm38) Q86K probably damaging Het
Fam71a T A 1: 191,164,022 (GRCm38) R141S probably benign Het
Fancm A T 12: 65,121,704 (GRCm38) M1614L probably benign Het
Fcgbp C T 7: 28,075,160 (GRCm38) T53I probably benign Het
Fpr3 T A 17: 17,971,015 (GRCm38) W183R probably damaging Het
Galnt13 G A 2: 54,854,645 (GRCm38) V119I probably benign Het
Gcfc2 T C 6: 81,923,812 (GRCm38) S36P probably benign Het
Gdap2 T A 3: 100,194,615 (GRCm38) D412E possibly damaging Het
Gm10184 T A 17: 89,910,306 (GRCm38) N4I possibly damaging Het
Gm12258 T C 11: 58,859,555 (GRCm38) C41R probably damaging Het
Grrp1 T C 4: 134,251,350 (GRCm38) *272W probably null Het
Hipk1 T G 3: 103,777,782 (GRCm38) E172D probably benign Het
Hmgcs1 T G 13: 119,703,591 (GRCm38) L326R probably benign Het
Hs6st1 C A 1: 36,068,886 (GRCm38) R77S probably damaging Het
Ifit3 A T 19: 34,587,173 (GRCm38) N40Y probably damaging Het
Il1a T A 2: 129,304,741 (GRCm38) Q144L possibly damaging Het
Itga7 A G 10: 128,957,811 (GRCm38) E1128G possibly damaging Het
Itih2 T C 2: 10,106,747 (GRCm38) D460G probably damaging Het
Ivns1abp G A 1: 151,351,558 (GRCm38) C39Y probably damaging Het
Kif22 G T 7: 127,027,839 (GRCm38) A646E probably damaging Het
Klhl29 T C 12: 5,091,307 (GRCm38) Y559C probably damaging Het
Klhl7 T A 5: 24,149,110 (GRCm38) probably null Het
Klhl9 A G 4: 88,721,993 (GRCm38) S4P probably benign Het
Klk10 A G 7: 43,782,880 (GRCm38) Q79R probably benign Het
Klk6 T C 7: 43,829,275 (GRCm38) probably null Het
Lamc2 C T 1: 153,166,263 (GRCm38) E42K probably benign Het
Lingo3 T C 10: 80,835,721 (GRCm38) D125G probably benign Het
Map1b T C 13: 99,432,739 (GRCm38) N1158S unknown Het
Masp1 T A 16: 23,494,637 (GRCm38) N183Y probably damaging Het
Mdga2 A G 12: 66,568,926 (GRCm38) Y636H probably benign Het
Micalcl T A 7: 112,381,610 (GRCm38) S264T probably damaging Het
Mif A G 10: 75,859,541 (GRCm38) V95A possibly damaging Het
Mmp17 G A 5: 129,595,088 (GRCm38) probably null Het
Mmp23 T C 4: 155,650,717 (GRCm38) R390G possibly damaging Het
Ncoa6 A C 2: 155,415,222 (GRCm38) S800R possibly damaging Het
Nfix G A 8: 84,726,526 (GRCm38) R300C probably damaging Het
Nr2e3 A T 9: 59,949,205 (GRCm38) S67R probably damaging Het
Odf2l T C 3: 145,149,036 (GRCm38) S545P possibly damaging Het
Olfr1256 G A 2: 89,835,172 (GRCm38) R258* probably null Het
Olfr172 C T 16: 58,760,853 (GRCm38) E108K probably damaging Het
Olfr591 T A 7: 103,173,451 (GRCm38) Y62F probably benign Het
Olfr845 C T 9: 19,338,652 (GRCm38) S64F probably benign Het
Olfr916 T G 9: 38,657,718 (GRCm38) I225L probably damaging Het
Olfr958 A T 9: 39,550,784 (GRCm38) V29E possibly damaging Het
Otog A T 7: 46,259,264 (GRCm38) H562L possibly damaging Het
Pcdh15 T C 10: 74,594,191 (GRCm38) V1250A probably damaging Het
Pde1c A G 6: 56,173,607 (GRCm38) V309A possibly damaging Het
Pfkfb4 A C 9: 109,007,305 (GRCm38) T134P probably damaging Het
Phc3 G T 3: 30,936,575 (GRCm38) Q498K possibly damaging Het
Phlpp1 T C 1: 106,392,319 (GRCm38) V1348A probably damaging Het
Pik3ap1 T C 19: 41,321,558 (GRCm38) D441G probably damaging Het
Pkd1l2 T C 8: 117,065,500 (GRCm38) probably null Het
Pla2g4a T C 1: 149,857,686 (GRCm38) probably null Het
Pola2 A T 19: 5,948,406 (GRCm38) I376N probably damaging Het
Pold2 T A 11: 5,876,833 (GRCm38) N34Y probably damaging Het
Ppp2r5c T C 12: 110,554,886 (GRCm38) L281P probably damaging Het
Prss46 A G 9: 110,849,635 (GRCm38) I29V probably benign Het
Ranbp6 A T 19: 29,811,446 (GRCm38) V502E probably benign Het
Rdh14 T C 12: 10,394,613 (GRCm38) F155L probably damaging Het
Rnaseh2a A T 8: 84,965,858 (GRCm38) probably null Het
Rpp30 A G 19: 36,094,385 (GRCm38) T118A possibly damaging Het
Rragd T C 4: 32,996,005 (GRCm38) F117L probably damaging Het
S100a2 T A 3: 90,591,292 (GRCm38) probably null Het
Sept12 T C 16: 4,996,476 (GRCm38) K43R probably damaging Het
Sh3tc2 A G 18: 62,008,488 (GRCm38) E1080G probably damaging Het
Slc26a9 A G 1: 131,750,677 (GRCm38) K27R probably damaging Het
Spata17 T A 1: 187,193,994 (GRCm38) K46N probably damaging Het
St14 A C 9: 31,108,215 (GRCm38) D103E probably benign Het
St6galnac2 T A 11: 116,684,347 (GRCm38) Q222L possibly damaging Het
Tdrd9 T C 12: 112,036,410 (GRCm38) V831A probably damaging Het
Tert A G 13: 73,642,056 (GRCm38) E843G probably damaging Het
Tex21 A G 12: 76,204,270 (GRCm38) V464A probably benign Het
Tmem232 T A 17: 65,484,501 (GRCm38) H124L probably damaging Het
Tmem5 A G 10: 122,090,479 (GRCm38) W243R probably damaging Het
Tnfrsf19 T G 14: 61,005,106 (GRCm38) S110R probably damaging Het
Tnnt3 A T 7: 142,515,825 (GRCm38) K272* probably null Het
Tnxb T C 17: 34,711,503 (GRCm38) L2054P probably damaging Het
Trcg1 A C 9: 57,242,465 (GRCm38) D440A probably benign Het
Trpm3 A G 19: 22,901,221 (GRCm38) E504G probably damaging Het
Trpm5 C T 7: 143,082,889 (GRCm38) R437H probably benign Het
Ttn T C 2: 76,741,167 (GRCm38) R18134G probably damaging Het
Uchl5 A C 1: 143,798,422 (GRCm38) M64L possibly damaging Het
Urb1 G A 16: 90,753,863 (GRCm38) R2034W probably damaging Het
Usp44 T A 10: 93,847,186 (GRCm38) C452* probably null Het
Uvssa G A 5: 33,413,934 (GRCm38) A641T probably damaging Het
Vmn1r204 T A 13: 22,557,078 (GRCm38) I293N probably benign Het
Vmn2r84 A T 10: 130,389,268 (GRCm38) C458S probably benign Het
Vmn2r85 T G 10: 130,425,919 (GRCm38) H183P probably damaging Het
Vps13d G T 4: 145,105,861 (GRCm38) T2825K probably benign Het
Zc3hc1 T A 6: 30,376,025 (GRCm38) I179F probably benign Het
Zfp112 A G 7: 24,125,785 (GRCm38) N393D probably damaging Het
Zfp558 A G 9: 18,456,563 (GRCm38) S310P possibly damaging Het
Zfp560 A C 9: 20,348,775 (GRCm38) probably null Het
Zfp668 C T 7: 127,867,080 (GRCm38) E311K probably benign Het
Zfp763 T A 17: 33,033,302 (GRCm38) M1L probably benign Het
Zfp947 A T 17: 22,145,832 (GRCm38) M287K probably benign Het
Other mutations in Olfr872
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01904:Olfr872 APN 9 20,260,290 (GRCm38) missense probably damaging 0.99
IGL02048:Olfr872 APN 9 20,260,488 (GRCm38) missense possibly damaging 0.79
IGL02232:Olfr872 APN 9 20,260,215 (GRCm38) missense probably damaging 1.00
IGL02314:Olfr872 APN 9 20,260,478 (GRCm38) missense probably benign 0.03
IGL03290:Olfr872 APN 9 20,260,260 (GRCm38) missense probably damaging 1.00
R0410:Olfr872 UTSW 9 20,260,501 (GRCm38) missense probably benign 0.03
R1482:Olfr872 UTSW 9 20,260,724 (GRCm38) missense possibly damaging 0.89
R4930:Olfr872 UTSW 9 20,260,017 (GRCm38) missense probably damaging 1.00
R5457:Olfr872 UTSW 9 20,260,278 (GRCm38) missense probably damaging 1.00
R5870:Olfr872 UTSW 9 20,260,578 (GRCm38) missense probably benign
R6141:Olfr872 UTSW 9 20,260,458 (GRCm38) missense probably benign 0.00
R7283:Olfr872 UTSW 9 20,260,259 (GRCm38) missense probably damaging 0.98
R8691:Olfr872 UTSW 9 20,260,451 (GRCm38) missense probably benign 0.36
R8882:Olfr872 UTSW 9 20,259,960 (GRCm38) missense probably benign 0.06
R9556:Olfr872 UTSW 9 20,260,355 (GRCm38) missense probably benign 0.00
R9618:Olfr872 UTSW 9 20,260,343 (GRCm38) missense possibly damaging 0.80
R9752:Olfr872 UTSW 9 20,259,908 (GRCm38) missense probably benign 0.10
X0025:Olfr872 UTSW 9 20,260,486 (GRCm38) missense probably benign 0.01
Predicted Primers PCR Primer

Sequencing Primer
Posted On 2014-04-13