Incidental Mutation 'R1148:Or5g9'
ID 102511
Institutional Source Beutler Lab
Gene Symbol Or5g9
Ensembl Gene ENSMUSG00000043226
Gene Name olfactory receptor family 5 subfamily G member 9
Synonyms Olfr1009, MOR175-3, GA_x6K02T2Q125-47195323-47196267
MMRRC Submission 039221-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.071) question?
Stock # R1148 (G1)
Quality Score 225
Status Validated
Chromosome 2
Chromosomal Location 85551751-85552695 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to A at 85552620 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 290 (Y290*)
Ref Sequence ENSEMBL: ENSMUSP00000150450 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055517] [ENSMUST00000216443]
AlphaFold Q8VFK1
Predicted Effect probably null
Transcript: ENSMUST00000055517
AA Change: Y290*
SMART Domains Protein: ENSMUSP00000061475
Gene: ENSMUSG00000043226
AA Change: Y290*

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 3.4e-55 PFAM
Pfam:7tm_1 41 290 4.3e-18 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000213600
Predicted Effect probably null
Transcript: ENSMUST00000216443
AA Change: Y290*
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 97.8%
  • 10x: 90.3%
  • 20x: 69.2%
Validation Efficiency 100% (35/35)
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: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2810021J22Rik T C 11: 58,767,544 (GRCm39) S14P probably damaging Het
Ablim2 T C 5: 35,966,605 (GRCm39) F178S probably damaging Het
Alg10b T C 15: 90,112,068 (GRCm39) F304S possibly damaging Het
Ank3 C T 10: 69,718,369 (GRCm39) S540F probably damaging Het
Arhgef16 T C 4: 154,365,346 (GRCm39) N590D probably benign Het
Arsi G A 18: 61,049,723 (GRCm39) G202E probably benign Het
Cfap58 C T 19: 47,976,943 (GRCm39) H731Y probably damaging Het
Cilp T A 9: 65,187,598 (GRCm39) L1231Q possibly damaging Het
Cyp4x1 A G 4: 114,983,752 (GRCm39) probably benign Het
Disp2 G A 2: 118,636,899 (GRCm39) probably null Het
Dnah5 T C 15: 28,421,836 (GRCm39) L3896P probably damaging Het
Dpp8 T C 9: 64,961,114 (GRCm39) probably null Het
Esp4 A C 17: 40,913,262 (GRCm39) N43T probably benign Het
Fat3 T C 9: 15,908,070 (GRCm39) D2644G probably damaging Het
Fgd5 A G 6: 91,964,612 (GRCm39) K124E probably benign Het
Folh1 T C 7: 86,410,938 (GRCm39) D268G probably damaging Het
Gm10608 CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA CAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA 9: 118,989,784 (GRCm39) probably null Het
Hexd A G 11: 121,112,093 (GRCm39) I438V probably benign Het
Lonp2 A G 8: 87,363,168 (GRCm39) E262G probably benign Het
Ly6h G T 15: 75,437,021 (GRCm39) S118R unknown Het
Mapk12 T C 15: 89,018,826 (GRCm39) Y203C probably damaging Het
Mapk15 A G 15: 75,870,004 (GRCm39) T375A probably benign Het
Morc2a A G 11: 3,628,557 (GRCm39) N337D probably benign Het
Nsd3 A G 8: 26,203,407 (GRCm39) D1307G probably benign Het
Osbpl11 T C 16: 33,047,582 (GRCm39) F515S probably damaging Het
Pcdh15 T C 10: 74,006,392 (GRCm39) V90A probably damaging Het
Ptpn4 T C 1: 119,612,270 (GRCm39) D41G probably damaging Het
Ric1 T C 19: 29,557,249 (GRCm39) Y445H probably benign Het
Sez6l2 C A 7: 126,560,984 (GRCm39) P483Q probably damaging Het
Sfi1 TCGC TC 11: 3,096,254 (GRCm39) probably null Het
Sfi1 CCTCTC CCTCTCTC 11: 3,127,419 (GRCm39) probably benign Het
Sgo2b A G 8: 64,379,889 (GRCm39) L981P probably damaging Het
Sh3d19 A G 3: 86,014,634 (GRCm39) D475G possibly damaging Het
Shprh T C 10: 11,089,226 (GRCm39) S1655P possibly damaging Het
Slc25a12 G A 2: 71,142,912 (GRCm39) probably benign Het
Strc A G 2: 121,202,558 (GRCm39) probably benign Het
Ttc22 G A 4: 106,480,228 (GRCm39) V161M probably damaging Het
Unc79 T C 12: 103,078,926 (GRCm39) L1504P probably damaging Het
Vldlr A G 19: 27,218,691 (GRCm39) N514S probably benign Het
Other mutations in Or5g9
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00920:Or5g9 APN 2 85,552,583 (GRCm39) missense probably damaging 1.00
IGL01862:Or5g9 APN 2 85,552,472 (GRCm39) missense probably damaging 0.99
IGL02868:Or5g9 APN 2 85,551,919 (GRCm39) missense probably benign 0.19
IGL02904:Or5g9 APN 2 85,552,099 (GRCm39) missense probably damaging 0.99
IGL03240:Or5g9 APN 2 85,552,675 (GRCm39) nonsense probably null
IGL03347:Or5g9 APN 2 85,552,151 (GRCm39) missense probably benign 0.01
R1148:Or5g9 UTSW 2 85,552,620 (GRCm39) nonsense probably null
R1446:Or5g9 UTSW 2 85,551,917 (GRCm39) missense probably damaging 0.99
R3782:Or5g9 UTSW 2 85,552,040 (GRCm39) missense probably damaging 1.00
R4343:Or5g9 UTSW 2 85,552,592 (GRCm39) missense probably damaging 1.00
R4836:Or5g9 UTSW 2 85,551,793 (GRCm39) missense probably benign
R4845:Or5g9 UTSW 2 85,551,836 (GRCm39) nonsense probably null
R5490:Or5g9 UTSW 2 85,552,666 (GRCm39) missense probably benign 0.01
R5534:Or5g9 UTSW 2 85,552,331 (GRCm39) missense probably benign 0.35
R5679:Or5g9 UTSW 2 85,552,390 (GRCm39) missense probably damaging 1.00
R6476:Or5g9 UTSW 2 85,551,928 (GRCm39) missense probably damaging 1.00
R6701:Or5g9 UTSW 2 85,552,675 (GRCm39) missense probably benign 0.28
R7024:Or5g9 UTSW 2 85,551,952 (GRCm39) missense probably damaging 1.00
R7140:Or5g9 UTSW 2 85,551,818 (GRCm39) missense probably damaging 0.97
R7174:Or5g9 UTSW 2 85,552,297 (GRCm39) missense possibly damaging 0.81
R8079:Or5g9 UTSW 2 85,552,387 (GRCm39) missense probably benign 0.07
R8082:Or5g9 UTSW 2 85,551,824 (GRCm39) missense probably benign 0.01
R8213:Or5g9 UTSW 2 85,551,845 (GRCm39) missense probably null 1.00
R9103:Or5g9 UTSW 2 85,552,527 (GRCm39) nonsense probably null
R9387:Or5g9 UTSW 2 85,551,806 (GRCm39) missense probably benign 0.00
R9508:Or5g9 UTSW 2 85,552,165 (GRCm39) missense possibly damaging 0.82
R9679:Or5g9 UTSW 2 85,552,482 (GRCm39) missense probably damaging 0.99
R9776:Or5g9 UTSW 2 85,552,145 (GRCm39) missense probably damaging 1.00
X0020:Or5g9 UTSW 2 85,552,322 (GRCm39) missense probably damaging 1.00
Predicted Primers
Posted On 2014-01-15