Incidental Mutation 'R5483:Or8u3-ps'
ID 434423
Institutional Source Beutler Lab
Gene Symbol Or8u3-ps
Ensembl Gene ENSMUSG00000050577
Gene Name olfactory receptor family 8 subfamily U member 3
Synonyms Olfr1038-ps, MOR185-3, GA_x6K02T2Q125-47591072-47592031
MMRRC Submission 043044-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.105) question?
Stock # R5483 (G1)
Quality Score 225
Status Not validated
Chromosome 2
Chromosomal Location 85950568-85953381 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to T at 85952962 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Stop codon at position 232 (Q232*)
Ref Sequence ENSEMBL: ENSMUSP00000149609 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000149775] [ENSMUST00000216665]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000149775
AA Change: Q232*
Predicted Effect probably null
Transcript: ENSMUST00000216665
AA Change: Q232*
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 97.5%
  • 10x: 94.8%
  • 20x: 89.2%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Cfap206 G T 4: 34,711,404 (GRCm39) Q498K probably benign Het
Dnmt3a A G 12: 3,949,615 (GRCm39) Y524C probably damaging Het
Dnttip2 A T 3: 122,070,446 (GRCm39) T554S probably damaging Het
Emc1 A G 4: 139,102,687 (GRCm39) T949A probably damaging Het
Enkur A T 2: 21,199,109 (GRCm39) F142I probably benign Het
Fbxo24 C T 5: 137,617,002 (GRCm39) A362T probably damaging Het
Heatr1 A G 13: 12,413,795 (GRCm39) H124R probably damaging Het
Hira T A 16: 18,788,290 (GRCm39) I1011N possibly damaging Het
Ipo5 T A 14: 121,157,450 (GRCm39) I96N probably benign Het
Kctd16 A G 18: 40,663,929 (GRCm39) I353V probably benign Het
Klf11 T A 12: 24,705,410 (GRCm39) L288* probably null Het
Kmt2a A T 9: 44,735,921 (GRCm39) probably benign Het
Lmbrd1 T C 1: 24,783,989 (GRCm39) Y373H probably damaging Het
Mlh1 G A 9: 111,060,126 (GRCm39) A584V possibly damaging Het
Ociad1 T C 5: 73,452,314 (GRCm39) F35S probably damaging Het
Or11l3 T A 11: 58,516,783 (GRCm39) I30F possibly damaging Het
Or6c208 T C 10: 129,223,526 (GRCm39) I8T probably benign Het
Pkd1l1 C T 11: 8,851,141 (GRCm39) probably null Het
Pole T A 5: 110,442,434 (GRCm39) D287E probably damaging Het
Polh G T 17: 46,483,671 (GRCm39) S531R probably benign Het
Prss29 A G 17: 25,541,177 (GRCm39) K207R probably benign Het
Rasgrp3 T G 17: 75,832,013 (GRCm39) S611R probably damaging Het
Rffl G T 11: 82,703,549 (GRCm39) probably null Het
Scrib A G 15: 75,939,508 (GRCm39) probably null Het
Serpinb3a T A 1: 106,974,899 (GRCm39) K211N probably benign Het
Slc22a3 C T 17: 12,683,354 (GRCm39) A170T probably damaging Het
Socs5 T G 17: 87,442,402 (GRCm39) F447L probably damaging Het
Srrm2 T A 17: 24,040,246 (GRCm39) S2393T probably damaging Het
Usp7 T A 16: 8,516,404 (GRCm39) Y585F probably benign Het
Vps39 A T 2: 120,153,564 (GRCm39) I670N probably benign Het
Other mutations in Or8u3-ps
AlleleSourceChrCoordTypePredicted EffectPPH Score
FR4737:Or8u3-ps UTSW 2 85,953,104 (GRCm39) frame shift probably null
R4276:Or8u3-ps UTSW 2 85,952,623 (GRCm39) missense probably damaging 1.00
R6464:Or8u3-ps UTSW 2 85,952,752 (GRCm39) missense possibly damaging 0.62
R6973:Or8u3-ps UTSW 2 85,953,198 (GRCm39) missense probably benign
R7508:Or8u3-ps UTSW 2 85,952,282 (GRCm39) missense possibly damaging 0.72
R7576:Or8u3-ps UTSW 2 85,952,720 (GRCm39) missense probably damaging 1.00
R7727:Or8u3-ps UTSW 2 85,952,840 (GRCm39) missense possibly damaging 0.93
R9401:Or8u3-ps UTSW 2 85,952,368 (GRCm39) missense possibly damaging 0.53
Predicted Primers PCR Primer
(F):5'- TCGCTTGACATATTGTGGACC -3'
(R):5'- AGAGGCATCTTTCACCTCTTTG -3'

Sequencing Primer
(F):5'- CGCTTGACATATTGTGGACCTAATG -3'
(R):5'- CCTAAGACTGTAGATGAGGGGGTTC -3'
Posted On 2016-10-06