Incidental Mutation 'R7061:Or8b9'
ID 548272
Institutional Source Beutler Lab
Gene Symbol Or8b9
Ensembl Gene ENSMUSG00000066749
Gene Name olfactory receptor family 8 subfamily B member 9
Synonyms Olfr877, MOR161-5, GA_x6K02T2PVTD-31540342-31541277
MMRRC Submission 045384-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.076) question?
Stock # R7061 (G1)
Quality Score 225.009
Status Validated
Chromosome 9
Chromosomal Location 37766116-37767051 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 37766942 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Aspartic acid at position 276 (V276D)
Ref Sequence ENSEMBL: ENSMUSP00000150698 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000086063] [ENSMUST00000213956]
AlphaFold Q8VF62
Predicted Effect possibly damaging
Transcript: ENSMUST00000086063
AA Change: V276D

PolyPhen 2 Score 0.878 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000083230
Gene: ENSMUSG00000066749
AA Change: V276D

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 1.4e-49 PFAM
Pfam:7tm_1 41 291 6.5e-20 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000213956
AA Change: V276D

PolyPhen 2 Score 0.878 (Sensitivity: 0.82; Specificity: 0.94)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 99% (68/69)
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: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aard G A 15: 51,903,617 (GRCm39) M13I probably benign Het
Abcb5 A C 12: 118,841,509 (GRCm39) Y979D probably damaging Het
Adgrb1 G C 15: 74,441,730 (GRCm39) V4L probably benign Het
Ap3b2 C T 7: 81,110,757 (GRCm39) R1006Q unknown Het
Bpifa6 A T 2: 153,834,236 (GRCm39) T343S probably benign Het
Celsr3 T A 9: 108,724,793 (GRCm39) C2957* probably null Het
Chd6 G A 2: 160,867,885 (GRCm39) Q428* probably null Het
Col5a1 C A 2: 27,915,690 (GRCm39) C191* probably null Het
Cpox A G 16: 58,491,223 (GRCm39) I145V possibly damaging Het
Csnk2a1 C T 2: 152,116,091 (GRCm39) R268C probably benign Het
Dclk2 A G 3: 86,739,038 (GRCm39) probably null Het
Dennd5a T C 7: 109,504,386 (GRCm39) E909G probably benign Het
Depdc1a T A 3: 159,228,489 (GRCm39) S414T possibly damaging Het
Dock5 A G 14: 68,007,703 (GRCm39) F1502S probably damaging Het
Dop1b G T 16: 93,558,951 (GRCm39) A448S probably benign Het
Dsg1c C A 18: 20,410,066 (GRCm39) N511K probably benign Het
Epc2 G T 2: 49,425,334 (GRCm39) R108L probably damaging Het
Erp44 T A 4: 48,219,375 (GRCm39) I147F probably benign Het
Evc T C 5: 37,476,446 (GRCm39) T368A possibly damaging Het
Fbxo41 G T 6: 85,452,448 (GRCm39) R738S probably benign Het
Fli1 T C 9: 32,335,518 (GRCm39) T305A probably damaging Het
Grk5 A G 19: 61,034,530 (GRCm39) T93A probably benign Het
Grm2 A T 9: 106,528,424 (GRCm39) N153K probably damaging Het
Helz A G 11: 107,540,003 (GRCm39) T1007A possibly damaging Het
Helz2 A G 2: 180,882,307 (GRCm39) L162P probably damaging Het
Hmgcr T A 13: 96,802,656 (GRCm39) Q81L possibly damaging Het
Hnrnpu T C 1: 178,163,691 (GRCm39) K218E unknown Het
Hydin A T 8: 111,329,920 (GRCm39) I4885F possibly damaging Het
Ibsp A G 5: 104,457,768 (GRCm39) probably null Het
Igfals T C 17: 25,099,281 (GRCm39) L124P probably damaging Het
Il24 T A 1: 130,811,108 (GRCm39) H142L possibly damaging Het
Iqca1l A G 5: 24,750,063 (GRCm39) M660T probably benign Het
Kcnh2 A T 5: 24,536,920 (GRCm39) H221Q probably benign Het
Man1a A G 10: 53,796,331 (GRCm39) S454P probably damaging Het
Meiosin A T 7: 18,834,053 (GRCm39) probably benign Het
Mfsd4b1 C T 10: 39,879,382 (GRCm39) V172M possibly damaging Het
Mical2 T A 7: 111,946,008 (GRCm39) I763K probably benign Het
Mybpc3 A G 2: 90,955,749 (GRCm39) I594M possibly damaging Het
Neo1 T A 9: 58,897,724 (GRCm39) R77S possibly damaging Het
Nlrp6 A G 7: 140,502,780 (GRCm39) I265M probably benign Het
Or52n5 T C 7: 104,587,883 (GRCm39) L50P probably damaging Het
Or5bw2 A G 7: 6,573,782 (GRCm39) Y264C probably damaging Het
Pcdhgb5 C A 18: 37,864,976 (GRCm39) P257Q probably benign Het
Phactr1 A G 13: 43,286,457 (GRCm39) D586G probably damaging Het
Pkn3 T A 2: 29,973,548 (GRCm39) probably null Het
Prob1 A T 18: 35,787,553 (GRCm39) S234T probably benign Het
Rab14 A T 2: 35,073,429 (GRCm39) L131* probably null Het
Rab5c G A 11: 100,610,789 (GRCm39) R40C probably damaging Het
Rhebl1 A G 15: 98,777,164 (GRCm39) L103P probably damaging Het
Rnf10 G T 5: 115,395,149 (GRCm39) F146L probably damaging Het
Rrbp1 T C 2: 143,831,087 (GRCm39) K360R possibly damaging Het
Slc6a9 C T 4: 117,725,261 (GRCm39) T575I probably benign Het
Smo A G 6: 29,760,229 (GRCm39) H776R probably damaging Het
Speer1f T C 5: 11,469,071 (GRCm39) V74A possibly damaging Het
Tns2 A G 15: 102,012,914 (GRCm39) M1V probably null Het
Ttn C A 2: 76,725,036 (GRCm39) probably benign Het
Ugt3a1 A T 15: 9,306,240 (GRCm39) M130L probably benign Het
Urb2 C T 8: 124,755,036 (GRCm39) H248Y probably benign Het
Vit A T 17: 78,932,585 (GRCm39) N564I probably damaging Het
Vmn1r60 A T 7: 5,547,310 (GRCm39) Y263* probably null Het
Vmn2r16 A T 5: 109,511,620 (GRCm39) Y609F probably damaging Het
Xpo7 T C 14: 70,908,512 (GRCm39) I876V probably benign Het
Zfp442 A G 2: 150,249,937 (GRCm39) I655T probably benign Het
Zfp574 T A 7: 24,779,622 (GRCm39) C215S possibly damaging Het
Zfp608 T C 18: 55,121,069 (GRCm39) T173A probably benign Het
Zfp69 A T 4: 120,788,598 (GRCm39) V239D possibly damaging Het
Other mutations in Or8b9
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01862:Or8b9 APN 9 37,766,477 (GRCm39) missense probably damaging 1.00
IGL02108:Or8b9 APN 9 37,766,234 (GRCm39) missense possibly damaging 0.88
IGL02474:Or8b9 APN 9 37,766,656 (GRCm39) missense probably benign 0.08
R0006:Or8b9 UTSW 9 37,766,516 (GRCm39) missense possibly damaging 0.95
R0893:Or8b9 UTSW 9 37,766,492 (GRCm39) missense probably damaging 1.00
R1051:Or8b9 UTSW 9 37,766,657 (GRCm39) missense probably damaging 0.99
R1432:Or8b9 UTSW 9 37,766,548 (GRCm39) missense possibly damaging 0.79
R1718:Or8b9 UTSW 9 37,766,749 (GRCm39) missense probably benign 0.03
R1864:Or8b9 UTSW 9 37,766,560 (GRCm39) missense probably damaging 1.00
R4120:Or8b9 UTSW 9 37,766,705 (GRCm39) missense possibly damaging 0.66
R4507:Or8b9 UTSW 9 37,766,201 (GRCm39) missense possibly damaging 0.90
R4900:Or8b9 UTSW 9 37,766,608 (GRCm39) missense probably benign
R5406:Or8b9 UTSW 9 37,766,515 (GRCm39) missense probably benign 0.02
R6813:Or8b9 UTSW 9 37,766,810 (GRCm39) missense possibly damaging 0.83
R7315:Or8b9 UTSW 9 37,766,543 (GRCm39) missense probably benign
R7500:Or8b9 UTSW 9 37,766,314 (GRCm39) missense probably damaging 1.00
R8021:Or8b9 UTSW 9 37,766,592 (GRCm39) missense probably damaging 1.00
R8188:Or8b9 UTSW 9 37,766,407 (GRCm39) missense probably benign 0.01
R9093:Or8b9 UTSW 9 37,766,294 (GRCm39) missense probably damaging 1.00
R9331:Or8b9 UTSW 9 37,766,710 (GRCm39) missense probably benign 0.03
R9373:Or8b9 UTSW 9 37,766,750 (GRCm39) missense probably damaging 0.97
R9696:Or8b9 UTSW 9 37,766,671 (GRCm39) missense probably benign 0.35
Z1088:Or8b9 UTSW 9 37,766,614 (GRCm39) missense probably benign 0.31
Z1177:Or8b9 UTSW 9 37,766,794 (GRCm39) missense possibly damaging 0.72
Predicted Primers PCR Primer
(F):5'- CATTGGAGTGCCCATTGTTAC -3'
(R):5'- GGTTTTCCTGCTGTTATAACACTGC -3'

Sequencing Primer
(F):5'- GTGCCCATTGTTACCATTTTTATATC -3'
(R):5'- GCTGTTATAACACTGCCTTTTATTTC -3'
Posted On 2019-05-13