Incidental Mutation 'R7751:Or9g3'
ID 628723
Institutional Source Beutler Lab
Gene Symbol Or9g3
Ensembl Gene ENSMUSG00000075210
Gene Name olfactory receptor family 9 subfamily G member 3
Synonyms MOR213-6, Olfr1012, GA_x6K02T2Q125-47239120-47238185
MMRRC Submission 045807-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.076) question?
Stock # R7751 (G1)
Quality Score 225.009
Status Validated
Chromosome 2
Chromosomal Location 85589783-85590718 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 85583836 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 44 (T44A)
Ref Sequence ENSEMBL: ENSMUSP00000151209 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000214255] [ENSMUST00000214958] [ENSMUST00000216831]
AlphaFold Q8VFJ7
Predicted Effect probably benign
Transcript: ENSMUST00000214255
Predicted Effect probably benign
Transcript: ENSMUST00000214958
Predicted Effect probably benign
Transcript: ENSMUST00000216831
AA Change: T44A

PolyPhen 2 Score 0.247 (Sensitivity: 0.91; Specificity: 0.88)
Meta Mutation Damage Score 0.0846 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency 98% (82/84)
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: 87 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca15 A T 7: 119,965,044 (GRCm39) I769F possibly damaging Het
Ackr1 A C 1: 173,159,779 (GRCm39) W247G probably damaging Het
Adgrl4 G A 3: 151,197,946 (GRCm39) G69S probably damaging Het
Agrn C T 4: 156,260,886 (GRCm39) S710N probably damaging Het
Aox3 A G 1: 58,218,494 (GRCm39) M1103V probably benign Het
Asb18 G A 1: 89,896,206 (GRCm39) A278V probably benign Het
B3gat2 A G 1: 23,801,945 (GRCm39) E77G probably benign Het
Camta1 T C 4: 151,232,863 (GRCm39) probably null Het
Cbll1 A T 12: 31,537,579 (GRCm39) I392N probably damaging Het
Ccdc113 A G 8: 96,264,829 (GRCm39) D113G possibly damaging Het
Cd79a T C 7: 24,599,092 (GRCm39) F148L probably benign Het
Chad T A 11: 94,455,999 (GRCm39) C26S probably damaging Het
Cog4 T C 8: 111,607,600 (GRCm39) F696L probably damaging Het
Csf2rb T G 15: 78,225,839 (GRCm39) S303R probably damaging Het
Cstpp1 A T 2: 91,214,118 (GRCm39) L79H probably damaging Het
Cubn C T 2: 13,365,176 (GRCm39) G1621R probably damaging Het
Dennd4c T A 4: 86,747,179 (GRCm39) N1454K probably benign Het
Dennd5b T C 6: 148,918,604 (GRCm39) I853V probably benign Het
Dnaaf11 T C 15: 66,321,412 (GRCm39) E243G probably benign Het
Dop1a A T 9: 86,389,783 (GRCm39) D561V probably benign Het
Dpysl4 A G 7: 138,669,456 (GRCm39) I45V probably benign Het
Ect2l A C 10: 18,045,153 (GRCm39) S301A possibly damaging Het
Elf2 A G 3: 51,165,035 (GRCm39) V323A probably damaging Het
Epcam C T 17: 87,947,904 (GRCm39) R125* probably null Het
Ephb4 T C 5: 137,363,937 (GRCm39) V612A probably damaging Het
Erich3 C T 3: 154,469,426 (GRCm39) R1293C unknown Het
F830045P16Rik C A 2: 129,302,367 (GRCm39) L408F probably damaging Het
Gask1a G A 9: 121,793,887 (GRCm39) V14I probably benign Het
Gm13102 T C 4: 143,835,787 (GRCm39) I485T probably benign Het
Gm16494 A T 17: 47,327,800 (GRCm39) L28* probably null Het
Grin2c A G 11: 115,144,696 (GRCm39) V610A probably damaging Het
Hacd2 T A 16: 34,922,434 (GRCm39) Y208N probably damaging Het
Hlf A T 11: 90,278,821 (GRCm39) F81Y probably damaging Het
Igfbp7 G A 5: 77,499,134 (GRCm39) A257V probably damaging Het
Il12a A T 3: 68,605,235 (GRCm39) N167I probably damaging Het
Il1r2 G A 1: 40,162,371 (GRCm39) C338Y probably damaging Het
Irf2bpl G T 12: 86,930,489 (GRCm39) H61Q probably damaging Het
Kansl1 A G 11: 104,314,890 (GRCm39) F383L probably benign Het
Kcnh8 A G 17: 53,268,871 (GRCm39) T863A probably damaging Het
Klhl36 C A 8: 120,596,397 (GRCm39) Q33K probably benign Het
Lrig2 A T 3: 104,401,985 (GRCm39) Y113* probably null Het
Lrrc36 T A 8: 106,178,667 (GRCm39) S287R possibly damaging Het
Mr1 A T 1: 155,005,054 (GRCm39) Y329N probably damaging Het
Muc5ac G C 7: 141,363,040 (GRCm39) G2117A unknown Het
Nectin4 G A 1: 171,211,326 (GRCm39) probably null Het
Nsrp1 A G 11: 76,940,097 (GRCm39) probably null Het
Or1e21 A T 11: 73,344,372 (GRCm39) I222N possibly damaging Het
Pcdh8 A T 14: 80,008,143 (GRCm39) I140N probably damaging Het
Pdzd8 A G 19: 59,333,208 (GRCm39) V271A probably damaging Het
Pex3 T A 10: 13,403,550 (GRCm39) I324L possibly damaging Het
Pira12 T A 7: 3,898,603 (GRCm39) I282F probably damaging Het
Pitpnm1 T A 19: 4,153,470 (GRCm39) F209I probably benign Het
Pkd1l3 GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA 8: 110,350,827 (GRCm39) probably benign Het
Pkhd1 T A 1: 20,271,149 (GRCm39) T3135S probably damaging Het
Pramel32 T C 4: 88,547,356 (GRCm39) D192G probably benign Het
Prdm16 T C 4: 154,412,756 (GRCm39) N1082S probably damaging Het
Psmd12 A T 11: 107,370,439 (GRCm39) I13F possibly damaging Het
Ptgs2 A T 1: 149,980,258 (GRCm39) I399F probably benign Het
Rasa3 A T 8: 13,618,708 (GRCm39) S830T probably benign Het
Rasgef1c A T 11: 49,861,120 (GRCm39) R362W probably damaging Het
Resf1 A G 6: 149,226,936 (GRCm39) probably benign Het
Rictor C T 15: 6,801,635 (GRCm39) S441L probably benign Het
Rnf217 C A 10: 31,393,415 (GRCm39) G389W probably damaging Het
Sec16b A T 1: 157,385,630 (GRCm39) D675V probably damaging Het
Serpinb12 A G 1: 106,877,401 (GRCm39) Y137C probably damaging Het
Slc2a5 T A 4: 150,227,591 (GRCm39) I470N probably damaging Het
Slc5a1 T C 5: 33,290,761 (GRCm39) I115T possibly damaging Het
Slco1a4 A T 6: 141,780,413 (GRCm39) S126T possibly damaging Het
St6galnac2 T C 11: 116,568,410 (GRCm39) D351G probably damaging Het
Stat4 G A 1: 52,121,711 (GRCm39) V357M possibly damaging Het
Taf4 G A 2: 179,573,822 (GRCm39) T682M probably damaging Het
Tdrd9 T A 12: 111,958,982 (GRCm39) C139S probably benign Het
Tmed9 G A 13: 55,741,054 (GRCm39) R23Q not run Het
Tmem150a A C 6: 72,336,028 (GRCm39) H205P probably damaging Het
Tns2 C A 15: 102,018,163 (GRCm39) L350I probably benign Het
Tpr A G 1: 150,295,646 (GRCm39) T964A probably benign Het
Traf3ip1 G T 1: 91,422,479 (GRCm39) probably benign Het
Trem2 G T 17: 48,653,567 (GRCm39) probably benign Het
Ttc14 G A 3: 33,863,590 (GRCm39) G666D unknown Het
Ulk1 T C 5: 110,957,078 (GRCm39) D40G probably damaging Het
Vmn1r30 A G 6: 58,412,397 (GRCm39) V145A probably benign Het
Vmn1r79 C T 7: 11,910,762 (GRCm39) Q215* probably null Het
Wnk2 G A 13: 49,231,493 (GRCm39) T16I unknown Het
Yme1l1 T C 2: 23,077,856 (GRCm39) probably null Het
Zbtb16 T A 9: 48,654,769 (GRCm39) H454L probably damaging Het
Zkscan5 A C 5: 145,157,676 (GRCm39) H726P probably damaging Het
Zrsr2-ps1 A G 11: 22,923,595 (GRCm39) Q123R possibly damaging Het
Other mutations in Or9g3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01799:Or9g3 APN 2 85,589,986 (GRCm39) missense probably benign 0.30
IGL02334:Or9g3 APN 2 85,590,503 (GRCm39) nonsense probably null
IGL03050:Or9g3 UTSW 2 85,589,785 (GRCm39) makesense probably null
R0399:Or9g3 UTSW 2 85,590,248 (GRCm39) missense possibly damaging 0.53
R1730:Or9g3 UTSW 2 85,590,586 (GRCm39) missense possibly damaging 0.91
R2142:Or9g3 UTSW 2 85,590,021 (GRCm39) missense probably benign 0.07
R2185:Or9g3 UTSW 2 85,590,363 (GRCm39) missense probably damaging 1.00
R2412:Or9g3 UTSW 2 85,590,024 (GRCm39) missense probably damaging 0.99
R3552:Or9g3 UTSW 2 85,590,237 (GRCm39) missense possibly damaging 0.46
R3785:Or9g3 UTSW 2 85,589,797 (GRCm39) missense probably benign 0.00
R4096:Or9g3 UTSW 2 85,590,040 (GRCm39) missense possibly damaging 0.55
R4097:Or9g3 UTSW 2 85,590,040 (GRCm39) missense possibly damaging 0.55
R5199:Or9g3 UTSW 2 85,590,558 (GRCm39) missense probably damaging 1.00
R5206:Or9g3 UTSW 2 85,589,967 (GRCm39) missense probably benign 0.31
R5444:Or9g3 UTSW 2 85,590,263 (GRCm39) missense probably benign 0.39
R5567:Or9g3 UTSW 2 85,589,994 (GRCm39) missense probably damaging 1.00
R5570:Or9g3 UTSW 2 85,589,994 (GRCm39) missense probably damaging 1.00
R5956:Or9g3 UTSW 2 85,584,183 (GRCm39) unclassified probably benign
R6406:Or9g3 UTSW 2 85,590,651 (GRCm39) missense possibly damaging 0.94
R7355:Or9g3 UTSW 2 85,584,023 (GRCm39) missense probably benign 0.03
R7534:Or9g3 UTSW 2 85,589,803 (GRCm39) missense probably benign 0.03
R8260:Or9g3 UTSW 2 85,589,820 (GRCm39) missense probably damaging 1.00
R8983:Or9g3 UTSW 2 85,584,251 (GRCm39) unclassified probably benign
R9025:Or9g3 UTSW 2 85,589,879 (GRCm39) missense possibly damaging 0.61
R9373:Or9g3 UTSW 2 85,590,275 (GRCm39) nonsense probably null
Predicted Primers PCR Primer
(F):5'- ATCTCTGGGCAACATGTGG -3'
(R):5'- TTCACTATAGGCCAGCCCAG -3'

Sequencing Primer
(F):5'- CTCTGGGCAACATGTGGATAATTTG -3'
(R):5'- TAGAAGAAGAACTGAGCCAGGCAAC -3'
Posted On 2020-06-17