Incidental Mutation 'R7247:Or8g19'
ID 563616
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 045310-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.054) question?
Stock # R7247 (G1)
Quality Score 225.009
Status Not validated
Chromosome 9
Chromosomal Location 39039463-39056368 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 39056153 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 252 (Y252*)
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: Y252*
Predicted Effect probably null
Transcript: ENSMUST00000216405
AA Change: Y252*
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.6%
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: 70 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 A G 11: 9,240,732 (GRCm39) E865G probably benign Het
Actrt2 A C 4: 154,751,880 (GRCm39) D85E probably benign Het
Ankrd55 A G 13: 112,472,787 (GRCm39) E153G probably damaging Het
Arfgef3 T A 10: 18,501,139 (GRCm39) H1037L probably benign Het
Camk2a A G 18: 61,076,277 (GRCm39) Y85C unknown Het
Caprin1 A T 2: 103,609,819 (GRCm39) V153E possibly damaging Het
Caskin2 G A 11: 115,692,722 (GRCm39) P688S probably benign Het
Catsper2 TAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCT TAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCT 2: 121,228,053 (GRCm39) probably benign Het
Ccdc116 T C 16: 16,957,555 (GRCm39) T535A possibly damaging Het
Cdh9 G A 15: 16,778,341 (GRCm39) R52H probably damaging Het
Cdk5rap2 A G 4: 70,255,666 (GRCm39) L406S probably damaging Het
Cep350 A G 1: 155,786,499 (GRCm39) M1449T probably damaging Het
Chst8 T A 7: 34,375,361 (GRCm39) K159N probably damaging Het
Dcdc2a A G 13: 25,286,374 (GRCm39) H136R probably benign Het
Dip2a C T 10: 76,108,366 (GRCm39) probably null Het
Dock2 G A 11: 34,605,340 (GRCm39) R260* probably null Het
Dscam A G 16: 96,622,008 (GRCm39) V481A probably damaging Het
E130308A19Rik A G 4: 59,690,502 (GRCm39) D112G probably damaging Het
Ezh2 T C 6: 47,510,708 (GRCm39) K634E probably damaging Het
Fcgr2b A G 1: 170,793,269 (GRCm39) probably null Het
Fgfrl1 T C 5: 108,851,365 (GRCm39) V94A possibly damaging Het
Gpr156 C A 16: 37,768,103 (GRCm39) N6K probably damaging Het
Gsdmc2 A T 15: 63,705,183 (GRCm39) F177I probably benign Het
Igkv4-54 T A 6: 69,608,842 (GRCm39) S26C probably damaging Het
Iglc3 T C 16: 18,884,191 (GRCm39) H80R Het
Immp1l G A 2: 105,767,401 (GRCm39) G87S probably damaging Het
Itgav A T 2: 83,555,179 (GRCm39) D34V probably damaging Het
Lrp1b G A 2: 41,159,224 (GRCm39) T1686I Het
Ltn1 T C 16: 87,206,275 (GRCm39) D935G probably benign Het
Map3k8 T C 18: 4,334,036 (GRCm39) D352G probably damaging Het
Map3k9 T C 12: 81,772,604 (GRCm39) K610E possibly damaging Het
Marchf4 G T 1: 72,491,637 (GRCm39) Y211* probably null Het
Marf1 A T 16: 13,944,957 (GRCm39) L1304Q probably damaging Het
Matcap1 A T 8: 106,011,331 (GRCm39) Y268N probably benign Het
Mecom A G 3: 30,194,505 (GRCm39) V5A unknown Het
Mep1a A T 17: 43,785,995 (GRCm39) V711D possibly damaging Het
Naca T A 10: 127,878,467 (GRCm39) D1166E unknown Het
Neb G T 2: 52,148,753 (GRCm39) P2598Q probably damaging Het
Notch4 A T 17: 34,791,491 (GRCm39) E546V probably damaging Het
Nudt18 A G 14: 70,815,422 (GRCm39) T12A unknown Het
Nvl A C 1: 180,939,851 (GRCm39) probably null Het
Obscn G T 11: 58,994,144 (GRCm39) C1579* probably null Het
Or4b13 G A 2: 90,083,165 (GRCm39) P56S probably damaging Het
Or51e2 T C 7: 102,391,551 (GRCm39) I220V probably damaging Het
Or6c5b T C 10: 129,246,051 (GRCm39) V272A probably damaging Het
Or7g33 A T 9: 19,448,629 (GRCm39) I199K probably benign Het
Oxa1l A T 14: 54,598,312 (GRCm39) M1L probably benign Het
Paqr9 A G 9: 95,442,246 (GRCm39) T79A possibly damaging Het
Plec A T 15: 76,061,543 (GRCm39) V2798E probably damaging Het
Potefam3f A G 8: 20,479,022 (GRCm39) N10S Het
Ptpn4 A T 1: 119,617,764 (GRCm39) *557R probably null Het
Ptprt T C 2: 161,375,443 (GRCm39) E1379G probably benign Het
Rad18 G T 6: 112,642,286 (GRCm39) T327K possibly damaging Het
Rps2 T A 17: 24,939,554 (GRCm39) I75N possibly damaging Het
Scgb2b2 A T 7: 31,003,021 (GRCm39) R39W probably damaging Het
Sh3d21 A G 4: 126,045,908 (GRCm39) F307S probably benign Het
Snap91 A G 9: 86,674,669 (GRCm39) V507A unknown Het
Srgap1 T A 10: 121,705,695 (GRCm39) Y243F probably damaging Het
Stim1 T A 7: 102,070,739 (GRCm39) probably null Het
Top2b T C 14: 16,416,962 (GRCm38) V1161A probably benign Het
Tpcn1 T C 5: 120,723,315 (GRCm39) D16G possibly damaging Het
Trank1 A T 9: 111,196,580 (GRCm39) I1535F probably damaging Het
Txnrd2 T C 16: 18,274,822 (GRCm39) F278L probably damaging Het
Ufl1 A T 4: 25,254,637 (GRCm39) D579E probably damaging Het
Vps45 T C 3: 95,948,717 (GRCm39) N346S probably benign Het
Vps51 T A 19: 6,127,419 (GRCm39) probably benign Het
Zfp536 T C 7: 37,268,631 (GRCm39) N262D probably benign Het
Zmynd10 A G 9: 107,425,976 (GRCm39) I103M possibly damaging Het
Zswim1 C T 2: 164,667,719 (GRCm39) H324Y possibly damaging Het
Zxdc T C 6: 90,361,155 (GRCm39) W507R unknown 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
R7520:Or8g19 UTSW 9 39,055,414 (GRCm39) missense probably benign
R7787:Or8g19 UTSW 9 39,055,548 (GRCm39) missense probably benign 0.22
R8360:Or8g19 UTSW 9 39,055,761 (GRCm39) nonsense probably null
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 PCR Primer
(F):5'- GGACTCAGTTCTGCAATTTAGATGTG -3'
(R):5'- TGTTCACATGATTCCTGCTTACATG -3'

Sequencing Primer
(F):5'- CTTGAATCTTGCATCCTCTAATACG -3'
(R):5'- GCATGGGTACAACAGTAG -3'
Posted On 2019-06-26