Incidental Mutation 'R3928:Or5p67'
ID 474874
Institutional Source Beutler Lab
Gene Symbol Or5p67
Ensembl Gene ENSMUSG00000109497
Gene Name olfactory receptor family 5 subfamily P member 67
Synonyms GA_x6K02T2PBJ9-10653693-10652749, Olfr492, MOR204-18
MMRRC Submission 040823-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.118) question?
Stock # R3928 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 107921937-107922881 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 107922232 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Threonine at position 217 (I217T)
Ref Sequence ENSEMBL: ENSMUSP00000146417 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000079865] [ENSMUST00000209545] [ENSMUST00000214605]
AlphaFold Q8VFD1
Predicted Effect probably benign
Transcript: ENSMUST00000079865
AA Change: I217T

PolyPhen 2 Score 0.160 (Sensitivity: 0.92; Specificity: 0.87)
Predicted Effect probably benign
Transcript: ENSMUST00000209545
Predicted Effect probably benign
Transcript: ENSMUST00000214605
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.5%
  • 20x: 95.6%
Validation Efficiency 100% (48/48)
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: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abr A T 11: 76,359,561 (GRCm39) H181Q probably benign Het
Atrx T C X: 104,923,523 (GRCm39) I157V possibly damaging Het
Birc6 A G 17: 74,918,170 (GRCm39) D1856G possibly damaging Het
Birc6 A G 17: 74,945,404 (GRCm39) T2811A probably damaging Het
Brsk2 T C 7: 141,552,155 (GRCm39) F108S probably damaging Het
Clasp2 C A 9: 113,735,173 (GRCm39) H1004N probably benign Het
Cntd1 G A 11: 101,178,345 (GRCm39) V315I probably benign Het
Col13a1 A G 10: 61,703,304 (GRCm39) probably benign Het
Ctps1 T A 4: 120,399,093 (GRCm39) H553L probably benign Het
Dpysl2 A G 14: 67,061,880 (GRCm39) I242T possibly damaging Het
Exoc3l C T 8: 106,017,549 (GRCm39) probably benign Het
Fam229a A G 4: 129,385,204 (GRCm39) probably benign Het
Fshr C T 17: 89,292,962 (GRCm39) R572H probably damaging Het
Gm5501 A G 18: 9,917,267 (GRCm39) noncoding transcript Het
Gmpr A G 13: 45,683,223 (GRCm39) I165V probably benign Het
Gnat3 G A 5: 18,208,892 (GRCm39) probably benign Het
H1f8 A G 6: 115,925,757 (GRCm39) K185E probably benign Het
H2-Q4 T G 17: 35,598,666 (GRCm39) L16R unknown Het
Hs2st1 T C 3: 144,140,389 (GRCm39) K311E possibly damaging Het
Kcnj15 A G 16: 95,097,368 (GRCm39) E330G possibly damaging Het
Kif3a A G 11: 53,461,441 (GRCm39) K29E probably benign Het
Krtap4-1 A G 11: 99,518,983 (GRCm39) V9A unknown Het
Lmntd2 C T 7: 140,791,117 (GRCm39) G432S probably damaging Het
Me3 T C 7: 89,482,898 (GRCm39) probably benign Het
Myo1d G T 11: 80,375,087 (GRCm39) R996S probably benign Het
Myo9a T A 9: 59,802,566 (GRCm39) W2018R probably damaging Het
Nphp3 G T 9: 103,888,929 (GRCm39) V265F probably damaging Het
Or10ak9 T C 4: 118,726,179 (GRCm39) L66P probably damaging Het
Or8c16 T C 9: 38,130,131 (GRCm39) M1T probably null Het
Pgp A G 17: 24,690,315 (GRCm39) E247G probably damaging Het
Pirb A T 7: 3,720,637 (GRCm39) L287Q probably benign Het
Plch1 G A 3: 63,675,044 (GRCm39) A202V probably damaging Het
Rbm11 G A 16: 75,389,932 (GRCm39) probably null Het
Scg5 T C 2: 113,622,230 (GRCm39) K124R probably damaging Het
Serpina3j A T 12: 104,285,916 (GRCm39) H357L probably damaging Het
St6gal2 A G 17: 55,803,324 (GRCm39) D353G possibly damaging Het
Tdpoz3 T C 3: 93,734,216 (GRCm39) I297T possibly damaging Het
Tdrd5 G A 1: 156,128,348 (GRCm39) T136I probably benign Het
Tfcp2l1 T A 1: 118,597,206 (GRCm39) I429K possibly damaging Het
Tnrc6c C T 11: 117,614,355 (GRCm39) R838W probably damaging Het
Top1 T C 2: 160,529,669 (GRCm39) probably benign Het
Trim61 A G 8: 65,465,969 (GRCm39) F431L probably benign Het
Trmo C T 4: 46,382,647 (GRCm39) G150S probably damaging Het
Vmn1r183 T C 7: 23,754,997 (GRCm39) S267P probably damaging Het
Xirp2 T A 2: 67,342,013 (GRCm39) F1418Y possibly damaging Het
Zfp114 T C 7: 23,880,467 (GRCm39) V271A possibly damaging Het
Zfp710 A G 7: 79,731,134 (GRCm39) R104G probably damaging Het
Other mutations in Or5p67
AlleleSourceChrCoordTypePredicted EffectPPH Score
R3056:Or5p67 UTSW 7 107,922,757 (GRCm39) missense possibly damaging 0.81
R5267:Or5p67 UTSW 7 107,922,185 (GRCm39) missense probably damaging 0.98
R5426:Or5p67 UTSW 7 107,922,017 (GRCm39) missense probably damaging 1.00
R5987:Or5p67 UTSW 7 107,922,254 (GRCm39) missense probably benign 0.00
R6800:Or5p67 UTSW 7 107,922,460 (GRCm39) missense probably benign 0.02
R6994:Or5p67 UTSW 7 107,922,101 (GRCm39) missense possibly damaging 0.57
R7516:Or5p67 UTSW 7 107,922,223 (GRCm39) missense probably damaging 1.00
R8139:Or5p67 UTSW 7 107,922,113 (GRCm39) missense probably benign 0.03
R8269:Or5p67 UTSW 7 107,922,776 (GRCm39) missense probably benign 0.03
R9440:Or5p67 UTSW 7 107,922,037 (GRCm39) missense probably benign
R9674:Or5p67 UTSW 7 107,922,271 (GRCm39) missense probably benign 0.25
Predicted Primers
Posted On 2017-04-14