Incidental Mutation 'R8932:Or9r7'
ID 690241
Institutional Source Beutler Lab
Gene Symbol Or9r7
Ensembl Gene ENSMUSG00000095804
Gene Name olfactory receptor family 9 subfamily R member 7
Synonyms Olfr824, GA_x6K02T2PULF-11797746-11796799, MOR210-3
MMRRC Submission 068776-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.075) question?
Stock # R8932 (G1)
Quality Score 225.009
Status Validated
Chromosome 10
Chromosomal Location 129961977-129962924 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 129962631 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Lysine at position 98 (N98K)
Ref Sequence ENSEMBL: ENSMUSP00000150606 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000074161] [ENSMUST00000214192] [ENSMUST00000215217]
AlphaFold Q8VFU4
Predicted Effect probably benign
Transcript: ENSMUST00000074161
AA Change: N98K

PolyPhen 2 Score 0.290 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000073794
Gene: ENSMUSG00000095804
AA Change: N98K

DomainStartEndE-ValueType
Pfam:7tm_4 34 311 4.6e-54 PFAM
Pfam:7tm_1 44 293 3e-20 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000214192
AA Change: N98K

PolyPhen 2 Score 0.290 (Sensitivity: 0.91; Specificity: 0.88)
Predicted Effect probably benign
Transcript: ENSMUST00000215217
AA Change: N98K

PolyPhen 2 Score 0.290 (Sensitivity: 0.91; Specificity: 0.88)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency 100% (67/67)
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: 72 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam34 G T 8: 44,105,192 (GRCm39) T151K probably benign Het
Adnp2 C T 18: 80,185,893 (GRCm39) G27S probably damaging Het
Ank3 A G 10: 69,660,292 (GRCm39) M265V probably benign Het
Aoc1l1 G A 6: 48,952,428 (GRCm39) E118K probably damaging Het
Apoe T C 7: 19,430,597 (GRCm39) D215G possibly damaging Het
Atp5f1b A G 10: 127,924,850 (GRCm39) I438V probably benign Het
Bckdha A G 7: 25,330,436 (GRCm39) S387P probably damaging Het
Camkk1 T C 11: 72,924,734 (GRCm39) F316L probably damaging Het
Carmil1 A G 13: 24,197,179 (GRCm39) Y158H Het
Ccdc148 T C 2: 58,894,054 (GRCm39) R29G probably benign Het
Ccdc39 A G 3: 33,884,274 (GRCm39) V356A probably benign Het
Cdan1 G A 2: 120,561,568 (GRCm39) Q66* probably null Het
Ckap4 A T 10: 84,364,290 (GRCm39) S258T probably benign Het
Col5a2 T C 1: 45,419,306 (GRCm39) D1258G probably benign Het
Col6a1 G A 10: 76,552,593 (GRCm39) P431L unknown Het
Cplane1 A G 15: 8,223,859 (GRCm39) Y874C probably damaging Het
Csn1s2a A G 5: 87,933,164 (GRCm39) I138V probably benign Het
Cyp19a1 C T 9: 54,083,861 (GRCm39) G176D probably benign Het
Dnah10 A G 5: 124,878,015 (GRCm39) E2700G possibly damaging Het
Eif3l T A 15: 78,960,006 (GRCm39) Y23* probably null Het
Fam72a A G 1: 131,456,502 (GRCm39) K22E probably benign Het
Golim4 A G 3: 75,805,351 (GRCm39) V258A probably benign Het
Gtf2ird2 C T 5: 134,237,739 (GRCm39) A272V probably benign Het
Hpse T C 5: 100,846,872 (GRCm39) T186A possibly damaging Het
Ift140 A T 17: 25,305,862 (GRCm39) Q816H probably benign Het
Iqca1 A T 1: 90,067,750 (GRCm39) I167N probably damaging Het
Iqgap1 A T 7: 80,401,141 (GRCm39) F515L probably benign Het
Itgb4 G A 11: 115,879,295 (GRCm39) R558H probably benign Het
Kcna10 G A 3: 107,101,419 (GRCm39) D17N probably damaging Het
Kcnj16 A G 11: 110,915,829 (GRCm39) I164V probably damaging Het
Lrrc55 G T 2: 85,026,615 (GRCm39) N136K probably damaging Het
Mdm4 A T 1: 132,940,382 (GRCm39) M50K probably benign Het
Mfge8 A G 7: 78,786,530 (GRCm39) S290P probably damaging Het
Mindy4 G A 6: 55,201,115 (GRCm39) D267N probably benign Het
Mllt10 T A 2: 18,128,617 (GRCm39) S199R probably benign Het
Mms22l T C 4: 24,533,029 (GRCm39) S436P probably damaging Het
Mpped2 A G 2: 106,697,395 (GRCm39) N290S possibly damaging Het
Mrgpra2a A G 7: 47,076,445 (GRCm39) L271P probably benign Het
Myrf T A 19: 10,200,931 (GRCm39) E247D probably benign Het
Ndrg3 A G 2: 156,782,299 (GRCm39) I189T possibly damaging Het
Nenf C T 1: 191,050,148 (GRCm39) E48K probably benign Het
Nlgn2 T A 11: 69,718,994 (GRCm39) N232Y probably damaging Het
Oog2 G T 4: 143,920,685 (GRCm39) M39I probably benign Het
Osbpl3 A T 6: 50,304,371 (GRCm39) N461K probably benign Het
P4ha1 A G 10: 59,175,130 (GRCm39) D30G possibly damaging Het
Pappa2 A T 1: 158,590,762 (GRCm39) C1631S probably damaging Het
Pigk A G 3: 152,445,871 (GRCm39) M161V possibly damaging Het
Prdm1 G T 10: 44,317,335 (GRCm39) S496Y probably damaging Het
Prkg2 T C 5: 99,095,299 (GRCm39) N624S possibly damaging Het
Rgs6 A G 12: 83,112,733 (GRCm39) D181G probably damaging Het
Sbf2 A G 7: 110,040,155 (GRCm39) probably null Het
Sbno2 A C 10: 79,898,042 (GRCm39) L728W probably damaging Het
Selenbp2 A T 3: 94,609,793 (GRCm39) I310F probably damaging Het
Shank3 T A 15: 89,432,986 (GRCm39) W1244R possibly damaging Het
Slc34a1 A C 13: 24,004,184 (GRCm39) I395L probably benign Het
Slf1 A T 13: 77,194,693 (GRCm39) D877E probably damaging Het
Smtn T C 11: 3,472,908 (GRCm39) S255G probably benign Het
Tbx2 T A 11: 85,725,533 (GRCm39) D161E probably damaging Het
Tex14 C A 11: 87,324,675 (GRCm39) L26M possibly damaging Het
Traf7 A G 17: 24,731,286 (GRCm39) F249S probably damaging Het
Trpm6 A G 19: 18,815,366 (GRCm39) K1151E possibly damaging Het
Ttc7b A G 12: 100,268,022 (GRCm39) V773A probably benign Het
Ttn G A 2: 76,747,912 (GRCm39) T4379I probably benign Het
Ttn G A 2: 76,602,854 (GRCm39) T18456I probably damaging Het
Ttn G C 2: 76,709,171 (GRCm39) L8703V unknown Het
Ubb T A 11: 62,442,979 (GRCm39) I3N probably damaging Het
Vmn1r209 A T 13: 22,990,343 (GRCm39) W116R probably damaging Het
Vmn1r75 A G 7: 11,614,838 (GRCm39) D190G probably damaging Het
Wdr12 T A 1: 60,130,202 (GRCm39) M70L probably benign Het
Wdr48 C A 9: 119,740,142 (GRCm39) T317K probably damaging Het
Zbtb5 A G 4: 44,993,962 (GRCm39) V474A probably benign Het
Zfp128 C T 7: 12,625,113 (GRCm39) R494C possibly damaging Het
Other mutations in Or9r7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01655:Or9r7 APN 10 129,962,860 (GRCm39) missense probably benign 0.45
IGL02391:Or9r7 APN 10 129,962,773 (GRCm39) missense possibly damaging 0.75
IGL03247:Or9r7 APN 10 129,962,584 (GRCm39) missense probably damaging 1.00
R0781:Or9r7 UTSW 10 129,962,522 (GRCm39) missense probably damaging 1.00
R1110:Or9r7 UTSW 10 129,962,522 (GRCm39) missense probably damaging 1.00
R1694:Or9r7 UTSW 10 129,962,123 (GRCm39) missense possibly damaging 0.93
R2069:Or9r7 UTSW 10 129,962,074 (GRCm39) missense possibly damaging 0.94
R2173:Or9r7 UTSW 10 129,962,372 (GRCm39) missense probably benign 0.10
R4078:Or9r7 UTSW 10 129,962,587 (GRCm39) missense probably damaging 1.00
R4864:Or9r7 UTSW 10 129,962,756 (GRCm39) nonsense probably null
R5556:Or9r7 UTSW 10 129,962,728 (GRCm39) missense probably damaging 1.00
R6704:Or9r7 UTSW 10 129,962,024 (GRCm39) nonsense probably null
R7624:Or9r7 UTSW 10 129,962,455 (GRCm39) missense probably damaging 0.98
R8013:Or9r7 UTSW 10 129,962,647 (GRCm39) missense probably damaging 1.00
R8049:Or9r7 UTSW 10 129,962,469 (GRCm39) nonsense probably null
R9256:Or9r7 UTSW 10 129,962,335 (GRCm39) missense possibly damaging 0.65
Predicted Primers PCR Primer
(F):5'- TCCACAGATATAGGAGCCAGC -3'
(R):5'- GTCTCCAGAAGCACAGGTTC -3'

Sequencing Primer
(F):5'- TATAGGAGCCAGCCACCAAACG -3'
(R):5'- AGAAGCACAGGTTCCCTTATTC -3'
Posted On 2021-11-19