Incidental Mutation 'R7842:Or52e19b'
ID 606379
Institutional Source Beutler Lab
Gene Symbol Or52e19b
Ensembl Gene ENSMUSG00000059874
Gene Name olfactory receptor family 52 subfamily E member 19B
Synonyms MOR32-2, GA_x6K02T2PBJ9-6092550-6092362, GA_x6K02T2PBJ9-6096387-6095449, Olfr604, Olfr603, MOR32-14_i
MMRRC Submission 045896-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.061) question?
Stock # R7842 (G1)
Quality Score 225.009
Status Validated
Chromosome 7
Chromosomal Location 103032269-103033207 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 103032783 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 142 (V142A)
Ref Sequence ENSEMBL: ENSMUSP00000151321 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000071844] [ENSMUST00000218246]
AlphaFold L7N1Y4
Predicted Effect probably benign
Transcript: ENSMUST00000071844
AA Change: V142A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000071744
Gene: ENSMUSG00000059874
AA Change: V142A

DomainStartEndE-ValueType
Pfam:7tm_4 33 311 1.7e-120 PFAM
Pfam:7TM_GPCR_Srsx 37 210 1.9e-10 PFAM
Pfam:7tm_1 43 293 5.4e-16 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000218246
AA Change: V142A

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency 99% (77/78)
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: 79 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700034J05Rik T C 6: 146,855,034 (GRCm39) T3A unknown Het
4933412E24Rik T C 15: 59,888,422 (GRCm39) E6G probably damaging Het
Abca6 A G 11: 110,087,523 (GRCm39) L1135P possibly damaging Het
Agps A G 2: 75,681,876 (GRCm39) D113G probably damaging Het
Ankhd1 G T 18: 36,780,881 (GRCm39) V1978L probably benign Het
Ankrd31 T A 13: 96,957,966 (GRCm39) probably null Het
Arhgap5 T A 12: 52,565,480 (GRCm39) M817K possibly damaging Het
Bdp1 C A 13: 100,235,637 (GRCm39) V105F probably damaging Het
Brdt A G 5: 107,496,454 (GRCm39) N189D possibly damaging Het
Ccdc180 A T 4: 45,909,428 (GRCm39) N532I probably benign Het
Ccnc A C 4: 21,730,480 (GRCm39) K39T probably damaging Het
Cfap251 T C 5: 123,392,487 (GRCm39) V207A unknown Het
Cfap57 C A 4: 118,411,952 (GRCm39) G1231* probably null Het
Chd7 A T 4: 8,854,115 (GRCm39) T1896S probably benign Het
Clk4 A T 11: 51,171,956 (GRCm39) H412L probably benign Het
Creld1 T C 6: 113,465,100 (GRCm39) L109P probably damaging Het
Cxxc4 A T 3: 133,946,093 (GRCm39) I225L possibly damaging Het
Cyp4f39 A T 17: 32,702,291 (GRCm39) R263W probably benign Het
Dennd10 G A 19: 60,819,317 (GRCm39) A263T not run Het
Dip2c T C 13: 9,656,569 (GRCm39) probably null Het
Dnah14 A G 1: 181,455,463 (GRCm39) T863A probably damaging Het
Dnah17 C A 11: 117,970,508 (GRCm39) probably null Het
Dnajc10 A G 2: 80,175,409 (GRCm39) K599E probably benign Het
Dnajc7 C A 11: 100,489,544 (GRCm39) R101L probably benign Het
Dnttip2 G A 3: 122,069,990 (GRCm39) E402K probably benign Het
Dusp22 T A 13: 30,852,774 (GRCm39) probably null Het
Egflam C A 15: 7,280,675 (GRCm39) R450M probably null Het
Eml5 C T 12: 98,760,394 (GRCm39) R1785Q probably damaging Het
Fam78b G T 1: 166,829,178 (GRCm39) R15L probably damaging Het
Fbxl5 A T 5: 43,915,945 (GRCm39) I489N probably damaging Het
Flt3 G A 5: 147,271,263 (GRCm39) P893S probably damaging Het
Gm17019 T C 5: 15,081,049 (GRCm39) M131V possibly damaging Het
Gm21560 T A 14: 6,216,262 (GRCm38) I194F probably benign Het
Gm28729 T C 9: 96,399,705 (GRCm39) D158G probably damaging Het
Gucy2c C T 6: 136,746,814 (GRCm39) probably null Het
Hectd1 C T 12: 51,819,343 (GRCm39) G1247S probably damaging Het
Ireb2 T A 9: 54,816,970 (GRCm39) I946K probably benign Het
Itgb4 A T 11: 115,873,531 (GRCm39) D249V probably benign Het
Klhdc7a A G 4: 139,694,549 (GRCm39) S133P probably damaging Het
Lsr A T 7: 30,665,437 (GRCm39) D172E possibly damaging Het
Macf1 T C 4: 123,420,702 (GRCm39) E184G probably benign Het
Map2 T A 1: 66,455,570 (GRCm39) D1421E probably benign Het
Map3k4 A T 17: 12,490,030 (GRCm39) L467H possibly damaging Het
Mogat1 T C 1: 78,499,502 (GRCm39) probably null Het
Mxra8 A G 4: 155,927,367 (GRCm39) D384G probably damaging Het
Myo15b A G 11: 115,762,321 (GRCm39) T1214A Het
Naip1 T C 13: 100,563,506 (GRCm39) Y553C probably damaging Het
Nln A T 13: 104,189,137 (GRCm39) I278K probably benign Het
Nsmaf T A 4: 6,435,109 (GRCm39) probably null Het
Nynrin A G 14: 56,102,553 (GRCm39) R741G probably damaging Het
Or4p8 A G 2: 88,727,305 (GRCm39) V212A possibly damaging Het
Or5d38 C T 2: 87,955,330 (GRCm39) probably benign Het
Or8j3 G T 2: 86,028,516 (GRCm39) Y193* probably null Het
Orc1 A G 4: 108,462,744 (GRCm39) H607R probably benign Het
Pate2 A T 9: 35,581,829 (GRCm39) Y41F probably damaging Het
Pcdhb20 A T 18: 37,638,112 (GRCm39) T213S possibly damaging Het
Pcm1 G A 8: 41,780,621 (GRCm39) E1858K possibly damaging Het
Pla2g2d A G 4: 138,506,089 (GRCm39) T59A probably damaging Het
Ppl C T 16: 4,906,725 (GRCm39) R1190H probably damaging Het
Prl2c2 A G 13: 13,179,907 (GRCm39) L2P probably benign Het
Proz G A 8: 13,113,406 (GRCm39) V76I probably benign Het
Prr36 A G 8: 4,260,953 (GRCm39) S955P probably benign Het
Pter T C 2: 12,983,352 (GRCm39) V119A probably damaging Het
Qrich1 T A 9: 108,433,567 (GRCm39) probably null Het
Rbm15b T C 9: 106,763,088 (GRCm39) E360G probably damaging Het
Skint11 G A 4: 114,101,968 (GRCm39) C327Y possibly damaging Het
Spag17 T A 3: 99,961,174 (GRCm39) S987T probably benign Het
Spata31f3 TCATTCAACACTTTGGAGAGCTCTGAACTCTGGCCATTCAACACTTTGGAGAGCTCTGAACTCTGGCCATTCAACACTTTGGAGAGCTCTGAACTCTGGTCATTCAACACTTTGG TCATTCAACACTTTGGAGAGCTCTGAACTCTGGCCATTCAACACTTTGGAGAGCTCTGAACTCTGGTCATTCAACACTTTGG 4: 42,871,823 (GRCm39) probably benign Het
Tbx1 T C 16: 18,405,365 (GRCm39) S100G unknown Het
Tiam2 C T 17: 3,568,399 (GRCm39) S1515L possibly damaging Het
Togaram1 C A 12: 65,013,233 (GRCm39) D161E probably damaging Het
Trhde A T 10: 114,532,003 (GRCm39) S366T possibly damaging Het
Ttc12 A G 9: 49,349,724 (GRCm39) I691T possibly damaging Het
Ube4a A G 9: 44,861,025 (GRCm39) probably null Het
Uggt2 A T 14: 119,235,516 (GRCm39) I1453N probably damaging Het
Unc79 T C 12: 103,058,313 (GRCm39) S972P probably damaging Het
Wdr20 G A 12: 110,704,649 (GRCm39) D63N probably benign Het
Wls T A 3: 159,578,816 (GRCm39) I126N probably benign Het
Xirp2 A G 2: 67,355,289 (GRCm39) D3350G probably benign Het
Other mutations in Or52e19b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00820:Or52e19b APN 7 103,032,672 (GRCm39) missense probably damaging 0.98
IGL01582:Or52e19b APN 7 103,032,806 (GRCm39) nonsense probably null
IGL01788:Or52e19b APN 7 103,032,770 (GRCm39) missense probably benign 0.00
IGL02837:Or52e19b UTSW 7 103,032,822 (GRCm39) missense probably damaging 1.00
R1807:Or52e19b UTSW 7 103,032,790 (GRCm39) missense probably benign 0.25
R2097:Or52e19b UTSW 7 103,032,840 (GRCm39) missense probably damaging 1.00
R2161:Or52e19b UTSW 7 103,032,407 (GRCm39) missense probably benign 0.01
R4870:Or52e19b UTSW 7 103,032,840 (GRCm39) missense probably damaging 1.00
R5116:Or52e19b UTSW 7 103,033,071 (GRCm39) missense probably benign 0.03
R6263:Or52e19b UTSW 7 103,032,403 (GRCm39) missense possibly damaging 0.88
R6385:Or52e19b UTSW 7 103,033,104 (GRCm39) missense possibly damaging 0.61
R6980:Or52e19b UTSW 7 103,032,303 (GRCm39) missense probably benign 0.01
R7474:Or52e19b UTSW 7 103,032,969 (GRCm39) missense probably damaging 0.99
R7754:Or52e19b UTSW 7 103,032,945 (GRCm39) missense probably damaging 1.00
R7947:Or52e19b UTSW 7 103,032,735 (GRCm39) missense possibly damaging 0.95
R7980:Or52e19b UTSW 7 103,032,970 (GRCm39) missense probably damaging 0.99
R8176:Or52e19b UTSW 7 103,033,071 (GRCm39) missense probably benign 0.03
R8523:Or52e19b UTSW 7 103,032,413 (GRCm39) missense probably benign 0.31
R8817:Or52e19b UTSW 7 103,032,825 (GRCm39) missense probably damaging 1.00
R8845:Or52e19b UTSW 7 103,032,357 (GRCm39) missense probably damaging 0.98
R8968:Or52e19b UTSW 7 103,032,667 (GRCm39) missense probably damaging 1.00
R9398:Or52e19b UTSW 7 103,032,487 (GRCm39) missense probably damaging 0.97
R9770:Or52e19b UTSW 7 103,032,613 (GRCm39) missense probably damaging 0.99
Z1177:Or52e19b UTSW 7 103,033,009 (GRCm39) missense probably benign 0.03
Predicted Primers PCR Primer
(F):5'- ACAGCCTGTAGGATCCAAGC -3'
(R):5'- ATCTTCTGGTTCAACCTTAGGG -3'

Sequencing Primer
(F):5'- CCTGTAGGATCCAAGCATAGG -3'
(R):5'- TCTGGTTCAACCTTAGGGAGATAAGC -3'
Posted On 2019-12-20