Incidental Mutation 'R8360:Or8g19'
ID 652153
Institutional Source Beutler Lab
Gene Symbol Or8g19
Ensembl Gene ENSMUSG00000049708
Gene Name olfactory receptor family 8 subfamily G member 19
Synonyms MOR171-6, GA_x6K02T2PVTD-32841223-32842158, Olfr27, MTPCR56, Olfr242, GA_x6K02T2KYVW-1037-120
MMRRC Submission 067734-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.054) question?
Stock # R8360 (G1)
Quality Score 225.009
Status Not validated
Chromosome 9
Chromosomal Location 39039463-39056368 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to T at 39055761 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Stop codon at position 122 (R122*)
Ref Sequence ENSEMBL: ENSMUSP00000151012 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000214052] [ENSMUST00000216405]
AlphaFold Q9EQ90
Predicted Effect probably null
Transcript: ENSMUST00000214052
AA Change: R122*
Predicted Effect probably null
Transcript: ENSMUST00000216405
AA Change: R122*
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.5%
  • 20x: 98.5%
Validation Efficiency 96% (43/45)
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
Abhd17b C T 19: 21,655,888 (GRCm39) Q57* probably null Het
Acad8 C T 9: 26,890,352 (GRCm39) A288T possibly damaging Het
Adamtsl3 G A 7: 82,197,187 (GRCm39) C711Y probably damaging Het
Ahcyl2 C A 6: 29,768,869 (GRCm39) D111E probably benign Het
Asxl3 T C 18: 22,649,174 (GRCm39) F388L probably benign Het
Bcr T A 10: 74,981,271 (GRCm39) S697T probably damaging Het
Catspere2 G A 1: 177,842,724 (GRCm39) V50M possibly damaging Het
Dgka C A 10: 128,563,997 (GRCm39) V451F probably damaging Het
Dnajc2 A T 5: 21,962,705 (GRCm39) C617S unknown Het
Erich3 C A 3: 154,469,991 (GRCm39) T1481K unknown Het
Golm2 A T 2: 121,697,632 (GRCm39) probably benign Het
Hdac2 T A 10: 36,874,059 (GRCm39) D396E probably benign Het
Hmgcs2 A T 3: 98,204,724 (GRCm39) D294V possibly damaging Het
Hnf1a A G 5: 115,091,391 (GRCm39) V434A possibly damaging Het
Il4ra T C 7: 125,169,138 (GRCm39) L130P probably damaging Het
Inpp5j T C 11: 3,449,767 (GRCm39) K672E probably damaging Het
Kif16b G A 2: 142,553,777 (GRCm39) A1007V probably benign Het
Kif26b T C 1: 178,743,938 (GRCm39) S1345P probably benign Het
Lrrc28 A T 7: 67,290,909 (GRCm39) D37E probably benign Het
Mlx G T 11: 100,978,140 (GRCm39) probably benign Het
Muc16 T C 9: 18,436,554 (GRCm39) H7878R probably benign Het
Mybpc1 C A 10: 88,409,359 (GRCm39) E32* probably null Het
Nebl C T 2: 17,465,298 (GRCm39) V18M probably benign Het
Nhsl3 C T 4: 129,117,995 (GRCm39) R268Q possibly damaging Het
Nlrp3 T C 11: 59,440,229 (GRCm39) V602A probably benign Het
Npepps G A 11: 97,120,665 (GRCm39) P532S probably benign Het
Or7g12 T A 9: 18,900,139 (GRCm39) M285K probably benign Het
Or8k53 T C 2: 86,177,668 (GRCm39) I147M possibly damaging Het
Pfdn1 G A 18: 36,584,214 (GRCm39) T40M probably benign Het
Pkd2 G T 5: 104,607,653 (GRCm39) E51* probably null Het
Prss40 T A 1: 34,599,876 (GRCm39) H37L probably benign Het
Rab11fip1 A T 8: 27,642,374 (GRCm39) C808* probably null Het
Rab3gap2 A T 1: 184,999,270 (GRCm39) probably benign Het
Sall3 C T 18: 81,017,232 (GRCm39) R232H probably benign Het
Sbk3 A G 7: 4,970,707 (GRCm39) F221L probably damaging Het
Sema7a T G 9: 57,862,974 (GRCm39) probably benign Het
Serpina3b C A 12: 104,104,962 (GRCm39) N379K probably benign Het
Ssbp4 A G 8: 71,052,039 (GRCm39) L208P probably benign Het
Stxbp5 C T 10: 9,688,003 (GRCm39) probably null Het
Tecrl A G 5: 83,448,764 (GRCm39) Y160H probably damaging Het
Tnc T C 4: 63,885,511 (GRCm39) I1773V probably benign Het
Ush2a A G 1: 188,198,468 (GRCm39) T1511A probably benign Het
Utp15 T C 13: 98,391,499 (GRCm39) N246S probably damaging Het
Vmn1r49 C T 6: 90,049,991 (GRCm39) A4T probably benign Het
Vmn2r57 A T 7: 41,049,640 (GRCm39) I703N probably damaging Het
Wdr93 A G 7: 79,398,974 (GRCm39) D36G probably damaging Het
Zfp334 A G 2: 165,225,278 (GRCm39) I8T probably benign Het
Other mutations in Or8g19
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00226:Or8g19 APN 9 39,056,053 (GRCm39) missense possibly damaging 0.94
IGL00905:Or8g19 APN 9 39,056,326 (GRCm39) missense probably damaging 1.00
IGL02346:Or8g19 APN 9 39,055,939 (GRCm39) missense probably damaging 1.00
R0117:Or8g19 UTSW 9 39,056,146 (GRCm39) missense probably damaging 1.00
R0118:Or8g19 UTSW 9 39,055,399 (GRCm39) start codon destroyed probably null 0.97
R0590:Or8g19 UTSW 9 39,056,017 (GRCm39) missense probably benign 0.01
R2915:Or8g19 UTSW 9 39,055,762 (GRCm39) missense possibly damaging 0.94
R4299:Or8g19 UTSW 9 39,056,295 (GRCm39) missense probably benign 0.11
R4367:Or8g19 UTSW 9 39,055,725 (GRCm39) missense probably damaging 0.98
R4663:Or8g19 UTSW 9 39,056,145 (GRCm39) missense probably damaging 0.97
R5276:Or8g19 UTSW 9 39,055,611 (GRCm39) missense probably damaging 1.00
R5503:Or8g19 UTSW 9 39,055,780 (GRCm39) missense probably benign 0.02
R5742:Or8g19 UTSW 9 39,055,974 (GRCm39) missense probably benign 0.07
R5986:Or8g19 UTSW 9 39,056,278 (GRCm39) missense probably null 1.00
R6801:Or8g19 UTSW 9 39,055,506 (GRCm39) missense probably benign 0.01
R7247:Or8g19 UTSW 9 39,056,153 (GRCm39) nonsense probably null
R7520:Or8g19 UTSW 9 39,055,414 (GRCm39) missense probably benign
R7787:Or8g19 UTSW 9 39,055,548 (GRCm39) missense probably benign 0.22
R8721:Or8g19 UTSW 9 39,055,386 (GRCm39) start gained probably benign
R8880:Or8g19 UTSW 9 39,055,899 (GRCm39) missense probably damaging 1.00
R8883:Or8g19 UTSW 9 39,056,083 (GRCm39) missense probably benign 0.00
R9143:Or8g19 UTSW 9 39,055,722 (GRCm39) missense possibly damaging 0.94
R9445:Or8g19 UTSW 9 39,055,766 (GRCm39) nonsense probably null
Predicted Primers
Posted On 2020-10-20