Incidental Mutation 'R0839:Or9e1'
ID 78123
Institutional Source Beutler Lab
Gene Symbol Or9e1
Ensembl Gene ENSMUSG00000094805
Gene Name olfactory receptor family 9 subfamily E member 1
Synonyms MOR222-1, Olfr311, GA_x6K02T2NKPP-565870-564944
MMRRC Submission 039018-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.080) question?
Stock # R0839 (G1)
Quality Score 225
Status Not validated
Chromosome 11
Chromosomal Location 58731942-58732868 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 58732478 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Isoleucine at position 179 (M179I)
Ref Sequence ENSEMBL: ENSMUSP00000150870 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071625] [ENSMUST00000216473]
AlphaFold Q5NC59
Predicted Effect probably benign
Transcript: ENSMUST00000071625
AA Change: M179I

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000071553
Gene: ENSMUSG00000094805
AA Change: M179I

DomainStartEndE-ValueType
Pfam:7tm_4 29 306 9e-52 PFAM
Pfam:7TM_GPCR_Srsx 33 215 1.7e-8 PFAM
Pfam:7tm_1 39 288 9.7e-20 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000214776
Predicted Effect probably benign
Transcript: ENSMUST00000216473
AA Change: M179I

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Coding Region Coverage
  • 1x: 99.5%
  • 3x: 99.0%
  • 10x: 97.8%
  • 20x: 96.1%
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: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca4 G A 3: 121,920,527 (GRCm39) V1083M probably damaging Het
Aco2 A G 15: 81,791,736 (GRCm39) probably null Het
AI661453 A T 17: 47,747,752 (GRCm39) Q8L probably null Het
Ankrd42 T C 7: 92,261,980 (GRCm39) D295G possibly damaging Het
Ccdc73 A T 2: 104,821,442 (GRCm39) I464L probably benign Het
Cdc5l A C 17: 45,704,073 (GRCm39) M717R probably benign Het
Col4a1 G A 8: 11,271,015 (GRCm39) P809S probably damaging Het
Dctn1 T C 6: 83,167,459 (GRCm39) M358T possibly damaging Het
Dgkz A G 2: 91,765,456 (GRCm39) S799P probably benign Het
Dna2 T C 10: 62,805,561 (GRCm39) C933R probably damaging Het
Dock6 T C 9: 21,729,188 (GRCm39) N1275S probably benign Het
Ect2l A G 10: 18,017,652 (GRCm39) I659T probably benign Het
Ets1 T A 9: 32,645,357 (GRCm39) Y201* probably null Het
Gle1 T A 2: 29,848,462 (GRCm39) C679S probably benign Het
Gm10118 T G 10: 63,762,643 (GRCm39) probably benign Het
Guk1 G A 11: 59,075,921 (GRCm39) R146C probably damaging Het
H2-Q7 A G 17: 35,658,688 (GRCm39) S109G probably damaging Het
Igfn1 A G 1: 135,882,418 (GRCm39) V2809A probably damaging Het
Izumo1 T A 7: 45,276,536 (GRCm39) D366E probably benign Het
Kctd20 A T 17: 29,176,872 (GRCm39) M1L possibly damaging Het
Lct C T 1: 128,214,346 (GRCm39) A1809T probably benign Het
Manea T C 4: 26,327,983 (GRCm39) I353V probably damaging Het
Mybl2 T C 2: 162,917,688 (GRCm39) Y65H probably benign Het
Myh11 C T 16: 14,021,042 (GRCm39) E1744K probably damaging Het
Neb T C 2: 52,167,560 (GRCm39) D1922G probably damaging Het
Nepro C A 16: 44,556,382 (GRCm39) D513E probably benign Het
Nnt A T 13: 119,531,192 (GRCm39) I185K possibly damaging Het
Npat A T 9: 53,456,480 (GRCm39) Q17L probably damaging Het
Nup155 A G 15: 8,175,071 (GRCm39) E956G possibly damaging Het
Or1e35 T A 11: 73,798,138 (GRCm39) Y60F probably damaging Het
Or1x6 A G 11: 50,939,254 (GRCm39) I107V probably benign Het
Or2a14 T A 6: 43,130,558 (GRCm39) F106L probably benign Het
Or4q3 A G 14: 50,583,545 (GRCm39) V118A probably damaging Het
Or8g18 A T 9: 39,149,146 (GRCm39) N191K possibly damaging Het
Or8g4 A T 9: 39,661,687 (GRCm39) I2L probably benign Het
Pah T C 10: 87,357,924 (GRCm39) S16P probably damaging Het
Pcdh15 C A 10: 74,462,614 (GRCm39) P1365Q probably null Het
Pds5b G T 5: 150,688,427 (GRCm39) V640F probably benign Het
Pgam5 A T 5: 110,414,996 (GRCm39) H72Q probably benign Het
Plagl2 C A 2: 153,074,461 (GRCm39) A147S probably damaging Het
Ppfia4 A T 1: 134,256,545 (GRCm39) L113Q probably null Het
Ppp1r12a T C 10: 108,034,722 (GRCm39) V89A probably damaging Het
Ptprc A G 1: 138,028,870 (GRCm39) Y443H possibly damaging Het
Ralgapb T C 2: 158,315,203 (GRCm39) probably null Het
Rgsl1 A G 1: 153,677,980 (GRCm39) probably null Het
Rubcn A C 16: 32,647,713 (GRCm39) I681M probably damaging Het
Scaf11 A G 15: 96,321,434 (GRCm39) L169S probably damaging Het
Scgb1b27 A G 7: 33,721,276 (GRCm39) K55E probably benign Het
Sos1 A T 17: 80,741,159 (GRCm39) I542N probably damaging Het
Syf2 T A 4: 134,663,374 (GRCm39) V182D probably damaging Het
Tapbp T C 17: 34,144,717 (GRCm39) V271A probably benign Het
Tmem33 T A 5: 67,421,651 (GRCm39) L60Q probably damaging Het
Tmf1 A G 6: 97,153,284 (GRCm39) V263A probably damaging Het
Vps13c T C 9: 67,806,020 (GRCm39) V798A probably benign Het
Zfp384 C A 6: 125,013,631 (GRCm39) D550E probably benign Het
Other mutations in Or9e1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02367:Or9e1 APN 11 58,732,338 (GRCm39) missense probably benign 0.10
H8786:Or9e1 UTSW 11 58,732,146 (GRCm39) missense probably benign 0.22
R0620:Or9e1 UTSW 11 58,732,269 (GRCm39) missense probably damaging 1.00
R0671:Or9e1 UTSW 11 58,732,681 (GRCm39) missense possibly damaging 0.94
R0827:Or9e1 UTSW 11 58,732,597 (GRCm39) missense probably damaging 1.00
R0932:Or9e1 UTSW 11 58,732,540 (GRCm39) missense possibly damaging 0.92
R1117:Or9e1 UTSW 11 58,732,641 (GRCm39) missense possibly damaging 0.64
R1533:Or9e1 UTSW 11 58,732,792 (GRCm39) missense probably damaging 1.00
R1540:Or9e1 UTSW 11 58,732,477 (GRCm39) missense probably benign 0.01
R1595:Or9e1 UTSW 11 58,732,478 (GRCm39) missense probably benign
R1826:Or9e1 UTSW 11 58,732,257 (GRCm39) missense probably benign
R2857:Or9e1 UTSW 11 58,732,708 (GRCm39) missense probably benign 0.42
R2858:Or9e1 UTSW 11 58,732,708 (GRCm39) missense probably benign 0.42
R2859:Or9e1 UTSW 11 58,732,708 (GRCm39) missense probably benign 0.42
R3438:Or9e1 UTSW 11 58,732,698 (GRCm39) nonsense probably null
R3765:Or9e1 UTSW 11 58,732,120 (GRCm39) missense probably damaging 1.00
R3831:Or9e1 UTSW 11 58,732,686 (GRCm39) missense probably damaging 0.99
R4858:Or9e1 UTSW 11 58,732,033 (GRCm39) missense possibly damaging 0.86
R5651:Or9e1 UTSW 11 58,732,317 (GRCm39) nonsense probably null
R5979:Or9e1 UTSW 11 58,732,666 (GRCm39) missense probably damaging 1.00
R6316:Or9e1 UTSW 11 58,732,768 (GRCm39) missense probably damaging 1.00
R6717:Or9e1 UTSW 11 58,732,113 (GRCm39) missense probably damaging 1.00
R7163:Or9e1 UTSW 11 58,732,012 (GRCm39) missense probably benign 0.12
R7605:Or9e1 UTSW 11 58,732,326 (GRCm39) missense probably benign 0.00
R8328:Or9e1 UTSW 11 58,732,460 (GRCm39) missense probably benign 0.00
Z1186:Or9e1 UTSW 11 58,732,032 (GRCm39) missense probably benign
Z1186:Or9e1 UTSW 11 58,732,569 (GRCm39) missense probably benign 0.16
Z1186:Or9e1 UTSW 11 58,731,945 (GRCm39) missense probably benign
Z1186:Or9e1 UTSW 11 58,731,907 (GRCm39) start gained probably benign
Z1186:Or9e1 UTSW 11 58,732,615 (GRCm39) missense probably benign
Z1187:Or9e1 UTSW 11 58,732,032 (GRCm39) missense probably benign
Z1187:Or9e1 UTSW 11 58,732,084 (GRCm39) missense probably benign
Z1187:Or9e1 UTSW 11 58,732,569 (GRCm39) missense probably benign 0.16
Z1187:Or9e1 UTSW 11 58,732,615 (GRCm39) missense probably benign
Z1187:Or9e1 UTSW 11 58,731,907 (GRCm39) start gained probably benign
Z1187:Or9e1 UTSW 11 58,731,945 (GRCm39) missense probably benign
Z1188:Or9e1 UTSW 11 58,731,945 (GRCm39) missense probably benign
Z1188:Or9e1 UTSW 11 58,731,907 (GRCm39) start gained probably benign
Z1188:Or9e1 UTSW 11 58,732,615 (GRCm39) missense probably benign
Z1188:Or9e1 UTSW 11 58,732,569 (GRCm39) missense probably benign 0.16
Z1188:Or9e1 UTSW 11 58,732,084 (GRCm39) missense probably benign
Z1188:Or9e1 UTSW 11 58,732,032 (GRCm39) missense probably benign
Z1189:Or9e1 UTSW 11 58,732,569 (GRCm39) missense probably benign 0.16
Z1189:Or9e1 UTSW 11 58,731,945 (GRCm39) missense probably benign
Z1189:Or9e1 UTSW 11 58,731,907 (GRCm39) start gained probably benign
Z1189:Or9e1 UTSW 11 58,732,615 (GRCm39) missense probably benign
Z1190:Or9e1 UTSW 11 58,731,945 (GRCm39) missense probably benign
Z1190:Or9e1 UTSW 11 58,731,907 (GRCm39) start gained probably benign
Z1190:Or9e1 UTSW 11 58,732,615 (GRCm39) missense probably benign
Z1190:Or9e1 UTSW 11 58,732,569 (GRCm39) missense probably benign 0.16
Z1190:Or9e1 UTSW 11 58,732,084 (GRCm39) missense probably benign
Z1190:Or9e1 UTSW 11 58,732,032 (GRCm39) missense probably benign
Z1191:Or9e1 UTSW 11 58,731,945 (GRCm39) missense probably benign
Z1191:Or9e1 UTSW 11 58,731,907 (GRCm39) start gained probably benign
Z1191:Or9e1 UTSW 11 58,732,615 (GRCm39) missense probably benign
Z1191:Or9e1 UTSW 11 58,732,569 (GRCm39) missense probably benign 0.16
Z1191:Or9e1 UTSW 11 58,732,084 (GRCm39) missense probably benign
Z1191:Or9e1 UTSW 11 58,732,032 (GRCm39) missense probably benign
Z1192:Or9e1 UTSW 11 58,732,032 (GRCm39) missense probably benign
Z1192:Or9e1 UTSW 11 58,731,945 (GRCm39) missense probably benign
Z1192:Or9e1 UTSW 11 58,731,907 (GRCm39) start gained probably benign
Z1192:Or9e1 UTSW 11 58,732,615 (GRCm39) missense probably benign
Z1192:Or9e1 UTSW 11 58,732,569 (GRCm39) missense probably benign 0.16
Predicted Primers PCR Primer
(F):5'- GGACATTTGCTACACCTCAGCCAC -3'
(R):5'- GGCCTCAGATACACAAAGCTTCCAG -3'

Sequencing Primer
(F):5'- TCAGGGGTCATCTCCTATCAAGAG -3'
(R):5'- GTTCCATAAAACAAGATGACCGTG -3'
Posted On 2013-10-16