Incidental Mutation 'R6752:Or5b114-ps1'
ID 530864
Institutional Source Beutler Lab
Gene Symbol Or5b114-ps1
Ensembl Gene
Gene Name olfactory receptor family 5 subfamily B member 114, pseudogene 1
Synonyms MOR202-21, Olfr1468-ps1, GA_x6K02T2RE5P-3706029-3706953
MMRRC Submission 044869-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.156) question?
Stock # R6752 (G1)
Quality Score 225.009
Status Validated
Chromosome 19
Chromosomal Location 13352328-13353249 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 13352890 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Histidine at position 188 (L188H)
Ref Sequence ENSEMBL: ENSMUSP00000146788 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000207287]
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000207287
AA Change: L188H
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.2%
  • 20x: 94.8%
Validation Efficiency 98% (55/56)
Allele List at MGI
Other mutations in this stock
Total: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acaca T C 11: 84,086,309 (GRCm39) L45S probably benign Het
Agbl2 G A 2: 90,633,418 (GRCm39) C518Y probably damaging Het
Akt3 A T 1: 176,877,756 (GRCm39) Y337* probably null Het
Aox1 T C 1: 58,086,398 (GRCm39) I101T probably benign Het
Arhgap23 T C 11: 97,343,074 (GRCm39) F241S probably damaging Het
Asmt A G X: 169,110,096 (GRCm39) M202V probably benign Het
Atp6v0a2 A G 5: 124,779,452 (GRCm39) E189G probably damaging Het
Birc2 G A 9: 7,857,345 (GRCm39) A376V probably benign Het
Ccbe1 C T 18: 66,209,378 (GRCm39) probably null Het
Chst2 C A 9: 95,286,802 (GRCm39) E515* probably null Het
Col12a1 A T 9: 79,540,706 (GRCm39) N2426K possibly damaging Het
Dmrt2 A G 19: 25,655,706 (GRCm39) N435S probably damaging Het
Dnah14 A G 1: 181,421,017 (GRCm39) K123E probably benign Het
Dock4 T A 12: 40,870,616 (GRCm39) L1452Q probably damaging Het
Galnt7 G A 8: 58,105,985 (GRCm39) R10C probably damaging Het
Gm16506 A G 14: 43,964,876 (GRCm39) I22T unknown Het
H2-Q6 A G 17: 35,647,103 (GRCm39) T292A probably damaging Het
Ifne A G 4: 88,798,319 (GRCm39) M33T probably benign Het
Igf2r G A 17: 12,933,831 (GRCm39) R808W probably damaging Het
Igfbp5 T C 1: 72,903,068 (GRCm39) E169G probably damaging Het
Inppl1 G A 7: 101,481,749 (GRCm39) R198* probably null Het
Irgm1 T C 11: 48,757,290 (GRCm39) T174A probably damaging Het
Itih3 C T 14: 30,645,446 (GRCm39) G21S possibly damaging Het
Klra4 G T 6: 130,038,991 (GRCm39) Q134K probably benign Het
Mfsd1 T A 3: 67,503,936 (GRCm39) Y309* probably null Het
Mrps10 A G 17: 47,688,740 (GRCm39) N162S probably damaging Het
Mtmr14 T C 6: 113,217,358 (GRCm39) F90S probably damaging Het
Myh15 A G 16: 49,003,290 (GRCm39) D1783G probably damaging Het
Myo3b A G 2: 70,119,856 (GRCm39) E972G probably damaging Het
Myt1 G T 2: 181,442,875 (GRCm39) V455F probably damaging Het
Nbea A T 3: 55,944,640 (GRCm39) S575T probably benign Het
Nbea T A 3: 55,875,730 (GRCm39) T1647S probably benign Het
Ntn4 A G 10: 93,570,037 (GRCm39) N466S probably benign Het
Or10ag52 A G 2: 87,043,388 (GRCm39) M51V probably benign Het
Or5h27 T A 16: 59,006,694 (GRCm39) N51Y probably damaging Het
Pcdhgb4 T A 18: 37,853,704 (GRCm39) I33N probably damaging Het
Pi4ka A G 16: 17,194,846 (GRCm39) L184P possibly damaging Het
Pom121l2 T G 13: 22,165,939 (GRCm39) F70C probably damaging Het
Psmb5 T C 14: 54,854,212 (GRCm39) T89A probably benign Het
Rab11fip2 T C 19: 59,895,475 (GRCm39) D471G probably damaging Het
Rnh1 A G 7: 140,743,354 (GRCm39) V207A probably benign Het
Sh3tc2 C A 18: 62,094,108 (GRCm39) T49N probably benign Het
Skint4 T C 4: 111,977,060 (GRCm39) M158T possibly damaging Het
Skint7 T A 4: 111,837,463 (GRCm39) H80Q probably benign Het
Smg1 A G 7: 117,762,539 (GRCm39) probably benign Het
Sostdc1 T C 12: 36,364,411 (GRCm39) V40A probably benign Het
Sptlc1 C A 13: 53,489,394 (GRCm39) K437N possibly damaging Het
Stat2 T C 10: 128,119,622 (GRCm39) F503L probably damaging Het
Syt16 A T 12: 74,275,987 (GRCm39) probably null Het
Tspyl1 T C 10: 34,158,583 (GRCm39) S103P probably benign Het
Ube4a A T 9: 44,837,246 (GRCm39) S1053R probably damaging Het
Vipr1 A G 9: 121,482,959 (GRCm39) N58S probably damaging Het
Zfp184 C A 13: 22,143,578 (GRCm39) A428E probably damaging Het
Zfp292 A C 4: 34,808,593 (GRCm39) F1484V possibly damaging Het
Zfp599 G A 9: 22,160,840 (GRCm39) H442Y probably damaging Het
Zfp944 G A 17: 22,558,500 (GRCm39) T249I probably benign Het
Zkscan14 T A 5: 145,132,316 (GRCm39) H405L probably damaging Het
Other mutations in Or5b114-ps1
AlleleSourceChrCoordTypePredicted EffectPPH Score
R6046:Or5b114-ps1 UTSW 19 13,352,698 (GRCm39) missense probably benign 0.16
R6141:Or5b114-ps1 UTSW 19 13,352,647 (GRCm39) missense probably benign 0.03
R6315:Or5b114-ps1 UTSW 19 13,352,769 (GRCm39) missense unknown
R6587:Or5b114-ps1 UTSW 19 13,352,977 (GRCm39) missense unknown
R6967:Or5b114-ps1 UTSW 19 13,352,815 (GRCm39) missense unknown
R7045:Or5b114-ps1 UTSW 19 13,352,336 (GRCm39) missense probably damaging 1.00
R7182:Or5b114-ps1 UTSW 19 13,353,208 (GRCm39) missense unknown
R7698:Or5b114-ps1 UTSW 19 13,352,404 (GRCm39) missense probably damaging 1.00
R7950:Or5b114-ps1 UTSW 19 13,352,431 (GRCm39) missense possibly damaging 0.78
R8673:Or5b114-ps1 UTSW 19 13,352,581 (GRCm39) missense probably benign 0.05
R8970:Or5b114-ps1 UTSW 19 13,353,117 (GRCm39) missense unknown
R9134:Or5b114-ps1 UTSW 19 13,352,613 (GRCm39) missense probably damaging 0.99
R9269:Or5b114-ps1 UTSW 19 13,353,004 (GRCm39) missense unknown
R9347:Or5b114-ps1 UTSW 19 13,352,553 (GRCm39) missense possibly damaging 0.88
Predicted Primers PCR Primer
(F):5'- ATGCAGCAGTGTGTAAGCC -3'
(R):5'- ATGATCGTCCCGTAGAAAATGG -3'

Sequencing Primer
(F):5'- GCAGCAGTGTGTAAGCCACTAC -3'
(R):5'- TCGTCCCGTAGAAAATGGACACTG -3'
Posted On 2018-08-01