Incidental Mutation 'R4619:Or52e19'
ID 345174
Institutional Source Beutler Lab
Gene Symbol Or52e19
Ensembl Gene ENSMUSG00000073953
Gene Name olfactory receptor family 52 subfamily E member 19
Synonyms Gm15117, ENSMUSG00000073953, Olfr596-ps1, Olfr596, GA_x6K02T2PBJ9-6019769-6019943
MMRRC Submission 041885-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.078) question?
Stock # R4619 (G1)
Quality Score 126
Status Validated
Chromosome 7
Chromosomal Location 102958930-102959868 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 102959165 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Isoleucine at position 79 (T79I)
Ref Sequence ENSEMBL: ENSMUSP00000149187 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000104880] [ENSMUST00000214577]
AlphaFold F8VQ26
Predicted Effect probably benign
Transcript: ENSMUST00000104880
AA Change: T79I

PolyPhen 2 Score 0.042 (Sensitivity: 0.94; Specificity: 0.83)
SMART Domains Protein: ENSMUSP00000100475
Gene: ENSMUSG00000073953
AA Change: T79I

DomainStartEndE-ValueType
Pfam:7tm_4 33 311 1.5e-121 PFAM
Pfam:7TM_GPCR_Srsx 37 210 5.1e-11 PFAM
Pfam:7tm_1 43 293 1.6e-15 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000214577
AA Change: T79I

PolyPhen 2 Score 0.042 (Sensitivity: 0.94; Specificity: 0.83)
Meta Mutation Damage Score 0.3701 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.5%
Validation Efficiency 100% (74/74)
Allele List at MGI
Other mutations in this stock
Total: 62 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110002E22Rik G A 3: 137,775,520 (GRCm39) V1570I probably damaging Het
Alx4 A G 2: 93,473,106 (GRCm39) R35G probably damaging Het
Apod T C 16: 31,116,211 (GRCm39) D173G probably benign Het
Atp8b3 G A 10: 80,361,858 (GRCm39) T731I possibly damaging Het
Birc6 A C 17: 74,947,145 (GRCm39) T2955P probably benign Het
Cdh15 G A 8: 123,587,612 (GRCm39) D179N probably damaging Het
Cntnap5c G T 17: 58,717,263 (GRCm39) V1282L probably benign Het
Crocc2 G A 1: 93,141,372 (GRCm39) R1175H probably benign Het
Dbh A G 2: 27,064,836 (GRCm39) D349G probably damaging Het
Dync1h1 A G 12: 110,605,278 (GRCm39) I2372V probably benign Het
Fer1l4 A T 2: 155,889,007 (GRCm39) W389R probably damaging Het
Fndc1 T C 17: 7,984,036 (GRCm39) T1297A unknown Het
Gart T C 16: 91,422,321 (GRCm39) N732S probably damaging Het
Gas2l2 T C 11: 83,313,924 (GRCm39) I463V probably benign Het
Gm5591 G A 7: 38,220,072 (GRCm39) S267L probably benign Het
Gzmk A G 13: 113,309,657 (GRCm39) V92A probably damaging Het
Hspg2 C T 4: 137,273,884 (GRCm39) R2680W probably damaging Het
Insyn2a A G 7: 134,520,270 (GRCm39) Y87H probably damaging Het
Kcnh3 G A 15: 99,131,982 (GRCm39) V646M probably damaging Het
Kcnk7 A C 19: 5,756,463 (GRCm39) I230L probably benign Het
Kif3b C T 2: 153,158,594 (GRCm39) R132* probably null Het
Klra5 T C 6: 129,885,776 (GRCm39) S128G probably benign Het
Krba1 C T 6: 48,383,282 (GRCm39) R4* probably null Het
Krt1c T A 15: 101,726,026 (GRCm39) I171F probably damaging Het
Lss A G 10: 76,372,089 (GRCm39) D148G probably benign Het
Mavs G T 2: 131,082,370 (GRCm39) A85S probably damaging Het
Mipep T C 14: 61,140,865 (GRCm39) C566R probably damaging Het
Myocd T A 11: 65,069,254 (GRCm39) probably benign Het
Ndufa9 C T 6: 126,804,498 (GRCm39) probably null Het
Nolc1 G A 19: 46,071,959 (GRCm39) G583D probably damaging Het
Nucb2 T C 7: 116,127,059 (GRCm39) probably null Het
Or1i2 T C 10: 78,448,409 (GRCm39) D22G probably benign Het
Or5p63 A T 7: 107,811,301 (GRCm39) I145N possibly damaging Het
Pank4 C A 4: 155,061,076 (GRCm39) D508E probably benign Het
Phb1 T A 11: 95,562,416 (GRCm39) probably benign Het
Pign T A 1: 105,449,715 (GRCm39) probably benign Het
Plec T C 15: 76,076,382 (GRCm39) K349E probably benign Het
Ppp1r3c A T 19: 36,711,743 (GRCm39) V9E possibly damaging Het
Rap1gap T A 4: 137,443,422 (GRCm39) V130D probably damaging Het
Senp3 T A 11: 69,567,944 (GRCm39) Y432F probably benign Het
Serpina3f T C 12: 104,183,549 (GRCm39) I137T possibly damaging Het
Slc46a3 T A 5: 147,823,540 (GRCm39) K101* probably null Het
Snph G A 2: 151,436,434 (GRCm39) Q96* probably null Het
Sptb A T 12: 76,630,581 (GRCm39) C2244* probably null Het
Srbd1 A T 17: 86,416,693 (GRCm39) F488L probably benign Het
Ssc5d A T 7: 4,932,524 (GRCm39) H396L probably damaging Het
Sulf1 A C 1: 12,856,876 (GRCm39) R42S probably damaging Het
Taf1a T A 1: 183,181,752 (GRCm39) probably benign Het
Thoc5 T A 11: 4,876,218 (GRCm39) M609K probably damaging Het
Tiam2 A T 17: 3,568,617 (GRCm39) I1588F probably damaging Het
Tmcc1 C T 6: 116,020,247 (GRCm39) V402I probably damaging Het
Tmprss15 T C 16: 78,818,358 (GRCm39) D524G probably damaging Het
Trbv31 T C 6: 41,534,901 (GRCm39) I21V probably benign Het
Vmn1r74 A T 7: 11,581,398 (GRCm39) T233S possibly damaging Het
Vmn1r74 G C 7: 11,581,403 (GRCm39) Q234H probably damaging Het
Vsx1 A T 2: 150,530,529 (GRCm39) S118T probably benign Het
Wnt9b G A 11: 103,621,949 (GRCm39) T236I probably benign Het
Zbtb21 T C 16: 97,751,092 (GRCm39) T1092A possibly damaging Het
Zc3hc1 G A 6: 30,387,523 (GRCm39) T52I probably benign Het
Zfp558 T A 9: 18,367,577 (GRCm39) N404Y possibly damaging Het
Zfp735 A T 11: 73,602,031 (GRCm39) D325V probably damaging Het
Zhx3 A T 2: 160,623,879 (GRCm39) M96K probably damaging Het
Other mutations in Or52e19
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00814:Or52e19 APN 7 102,959,014 (GRCm39) missense probably benign 0.03
IGL01917:Or52e19 APN 7 102,959,564 (GRCm39) nonsense probably null
G1patch:Or52e19 UTSW 7 102,959,561 (GRCm39) missense probably damaging 1.00
R0601:Or52e19 UTSW 7 102,959,371 (GRCm39) missense probably damaging 1.00
R0908:Or52e19 UTSW 7 102,959,780 (GRCm39) missense possibly damaging 0.56
R1762:Or52e19 UTSW 7 102,959,428 (GRCm39) missense probably damaging 1.00
R1772:Or52e19 UTSW 7 102,959,449 (GRCm39) missense possibly damaging 0.94
R1806:Or52e19 UTSW 7 102,959,432 (GRCm39) missense probably damaging 1.00
R2035:Or52e19 UTSW 7 102,959,463 (GRCm39) missense probably damaging 1.00
R2365:Or52e19 UTSW 7 102,959,380 (GRCm39) missense probably benign 0.00
R3827:Or52e19 UTSW 7 102,959,009 (GRCm39) missense probably benign 0.12
R4241:Or52e19 UTSW 7 102,959,868 (GRCm39) makesense probably null
R4620:Or52e19 UTSW 7 102,959,165 (GRCm39) missense probably benign 0.04
R6279:Or52e19 UTSW 7 102,959,636 (GRCm39) missense probably benign
R6300:Or52e19 UTSW 7 102,959,636 (GRCm39) missense probably benign
R6505:Or52e19 UTSW 7 102,959,000 (GRCm39) missense probably benign 0.00
R6725:Or52e19 UTSW 7 102,959,561 (GRCm39) missense probably damaging 1.00
R7175:Or52e19 UTSW 7 102,959,054 (GRCm39) missense probably benign 0.22
R7708:Or52e19 UTSW 7 102,959,768 (GRCm39) missense probably damaging 1.00
R8855:Or52e19 UTSW 7 102,959,168 (GRCm39) missense probably damaging 1.00
R9035:Or52e19 UTSW 7 102,959,186 (GRCm39) missense probably damaging 1.00
R9162:Or52e19 UTSW 7 102,958,927 (GRCm39) start gained probably benign
R9489:Or52e19 UTSW 7 102,959,452 (GRCm39) missense probably benign 0.00
R9799:Or52e19 UTSW 7 102,959,065 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TTCCTGGGCTGGAAGCTTTC -3'
(R):5'- TCCCTATTACAACCGATGCC -3'

Sequencing Primer
(F):5'- CCATATCTGGATAGCCTTTCCTTTC -3'
(R):5'- CCACCACTTTGTTGGTGAGAATAGAG -3'
Posted On 2015-09-25