Incidental Mutation 'R8840:Or8g29-ps1'
ID 674374
Institutional Source Beutler Lab
Gene Symbol Or8g29-ps1
Ensembl Gene
Gene Name olfactory receptor family 8 subfamily G member 29, pseudogene 1
Synonyms Olfr947-ps1, GA_x6K02T2PVTD-32987171-32986232, MOR171-43
MMRRC Submission 068668-MU
Accession Numbers
Essential gene? Not available question?
Stock # R8840 (G1)
Quality Score 225.009
Status Validated
Chromosome 9
Chromosomal Location 39199220-39210777 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 39201018 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Isoleucine at position 56 (T56I)
Ref Sequence ENSEMBL: ENSMUSP00000150686 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000214075] [ENSMUST00000214936] [ENSMUST00000215471]
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000214075
AA Change: T56I
Predicted Effect unknown
Transcript: ENSMUST00000214936
AA Change: T56I
Predicted Effect unknown
Transcript: ENSMUST00000215471
AA Change: T56I
Meta Mutation Damage Score 0.0852 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.3%
Validation Efficiency 100% (46/46)
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Anapc4 G A 5: 53,016,473 (GRCm39) D484N probably damaging Het
Antxr2 T A 5: 98,152,769 (GRCm39) L109F probably damaging Het
Arhgap9 A G 10: 127,161,009 (GRCm39) T179A possibly damaging Het
Atp6v1b1 A T 6: 83,733,845 (GRCm39) I359F Het
Btnl1 A G 17: 34,604,577 (GRCm39) T453A probably benign Het
Bub1 T C 2: 127,649,927 (GRCm39) I644V probably benign Het
Ccdc163 T A 4: 116,567,483 (GRCm39) probably null Het
Ccdc8 T A 7: 16,728,642 (GRCm39) F44I probably damaging Het
Ccz1 T C 5: 143,940,982 (GRCm39) I191V probably damaging Het
Cldn1 T C 16: 26,190,286 (GRCm39) K31E possibly damaging Het
Ctr9 A G 7: 110,642,237 (GRCm39) D321G probably damaging Het
Dmxl2 T C 9: 54,309,139 (GRCm39) N1871D possibly damaging Het
Dop1b A G 16: 93,607,005 (GRCm39) I2103V probably benign Het
Dscaml1 A G 9: 45,634,718 (GRCm39) E1211G probably damaging Het
Eppk1 T A 15: 75,994,094 (GRCm39) D929V probably benign Het
Fam151a T C 4: 106,602,819 (GRCm39) V246A probably benign Het
Fsip2 A G 2: 82,821,606 (GRCm39) I5780V probably benign Het
Gart A T 16: 91,433,010 (GRCm39) M313K probably benign Het
Gnl1 T G 17: 36,293,486 (GRCm39) L224V probably damaging Het
Hectd3 T C 4: 116,855,604 (GRCm39) V368A probably benign Het
Ibsp C T 5: 104,458,006 (GRCm39) A181V probably benign Het
Kdm1a T C 4: 136,287,716 (GRCm39) E421G probably damaging Het
Kmt2a A T 9: 44,721,016 (GRCm39) Y3831N unknown Het
Meltf T C 16: 31,716,020 (GRCm39) L733P probably damaging Het
Nod2 T C 8: 89,399,379 (GRCm39) F898L probably benign Het
Npr3 A T 15: 11,905,329 (GRCm39) Y133N probably damaging Het
Pkd1l3 T C 8: 110,349,842 (GRCm39) V229A unknown Het
Pramel25 C A 4: 143,521,638 (GRCm39) T418K probably damaging Het
Primpol A T 8: 47,046,731 (GRCm39) F188L probably damaging Het
Rbm15 A G 3: 107,240,305 (GRCm39) V31A probably benign Het
Robo2 T A 16: 73,782,570 (GRCm39) D322V probably damaging Het
Rpl3l A G 17: 24,952,711 (GRCm39) N114S probably damaging Het
Sacs A G 14: 61,429,177 (GRCm39) D412G probably benign Het
Sbno2 A G 10: 79,893,360 (GRCm39) S1314P probably damaging Het
Sez6 A G 11: 77,867,313 (GRCm39) D770G probably damaging Het
Skint7 T C 4: 111,845,183 (GRCm39) F332L probably benign Het
Spaca6 A T 17: 18,051,365 (GRCm39) I34F possibly damaging Het
Suclg2 T A 6: 95,546,615 (GRCm39) E287V probably damaging Het
Trhr2 T C 8: 123,085,621 (GRCm39) Y121C probably damaging Het
Ttn T G 2: 76,606,371 (GRCm39) D18146A probably damaging Het
Wdr3 G A 3: 100,057,253 (GRCm39) T450I probably damaging Het
Xab2 A G 8: 3,663,254 (GRCm39) F470L probably benign Het
Ythdc2 A G 18: 44,993,691 (GRCm39) H912R probably damaging Het
Zfp64 A T 2: 168,768,635 (GRCm39) S326T probably benign Het
Zswim4 C T 8: 84,940,699 (GRCm39) R800Q probably damaging Het
Other mutations in Or8g29-ps1
AlleleSourceChrCoordTypePredicted EffectPPH Score
R6957:Or8g29-ps1 UTSW 9 39,200,577 (GRCm39) missense unknown
R7203:Or8g29-ps1 UTSW 9 39,200,589 (GRCm39) missense unknown
R9249:Or8g29-ps1 UTSW 9 39,200,602 (GRCm39) missense unknown
R9278:Or8g29-ps1 UTSW 9 39,200,781 (GRCm39) missense probably benign 0.15
R9590:Or8g29-ps1 UTSW 9 39,201,076 (GRCm39) missense unknown
R9755:Or8g29-ps1 UTSW 9 39,200,970 (GRCm39) missense possibly damaging 0.46
Predicted Primers PCR Primer
(F):5'- TGGCAACATAGCGGTCATATG -3'
(R):5'- TTGTTCTCTTCCAGATCTGAATGGAG -3'

Sequencing Primer
(F):5'- ACATAGCGGTCATATGCCATTGC -3'
(R):5'- TCTTCCAGATCTGAATGGAGGACATG -3'
Posted On 2021-07-15