Incidental Mutation 'R4469:Or12d14-ps1'
ID 329342
Institutional Source Beutler Lab
Gene Symbol Or12d14-ps1
Ensembl Gene ENSMUSG00000095858
Gene Name olfactory receptor family 12 subfamily D member 14, pseudogene 1
Synonyms GA_x6K02T2PSCP-1823235-1824161, MOR250-5, Olfr104-ps, Olfr104
MMRRC Submission 041726-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.203) question?
Stock # R4469 (G1)
Quality Score 225
Status Validated
Chromosome 17
Chromosomal Location 37673011-37673990 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 37673528 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Methionine at position 170 (I170M)
Ref Sequence ENSEMBL: ENSMUSP00000154728 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000178766] [ENSMUST00000215398]
AlphaFold A0A2I3BRX0
Predicted Effect possibly damaging
Transcript: ENSMUST00000178766
AA Change: I170M

PolyPhen 2 Score 0.585 (Sensitivity: 0.88; Specificity: 0.91)
Predicted Effect probably benign
Transcript: ENSMUST00000215398
AA Change: I173M

PolyPhen 2 Score 0.403 (Sensitivity: 0.89; Specificity: 0.89)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000216996
Predicted Effect noncoding transcript
Transcript: ENSMUST00000219092
Meta Mutation Damage Score 0.1795 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.9%
  • 20x: 94.4%
Validation Efficiency 100% (52/52)
Allele List at MGI
Other mutations in this stock
Total: 49 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4833420G17Rik A G 13: 119,606,345 (GRCm39) K196E probably damaging Het
Ackr1 T C 1: 173,160,112 (GRCm39) probably null Het
Adgra1 C T 7: 139,455,977 (GRCm39) T535I probably damaging Het
Ankrd11 A G 8: 123,623,326 (GRCm39) Y310H probably damaging Het
Arhgef5 T C 6: 43,252,033 (GRCm39) I928T probably benign Het
Arsi G A 18: 61,049,723 (GRCm39) G202E probably benign Het
Asb4 C A 6: 5,423,409 (GRCm39) F185L probably benign Het
Ces2g A T 8: 105,692,602 (GRCm39) I301F probably benign Het
Chd1 T C 17: 15,980,657 (GRCm39) I1308T probably damaging Het
Cntnap4 A T 8: 113,391,898 (GRCm39) N121I probably damaging Het
Csf1 C T 3: 107,657,997 (GRCm39) probably null Het
Dnah7a T A 1: 53,483,685 (GRCm39) H3364L probably benign Het
Dnmt3c A G 2: 153,562,280 (GRCm39) T555A possibly damaging Het
Dst A G 1: 34,230,923 (GRCm39) T3017A probably benign Het
Efcab7 A G 4: 99,766,901 (GRCm39) D482G possibly damaging Het
Fbxl5 A G 5: 43,925,528 (GRCm39) V154A probably damaging Het
Flt3 T C 5: 147,312,454 (GRCm39) silent Het
G6pd2 A T 5: 61,966,288 (GRCm39) Y21F probably benign Het
Gm9376 C T 14: 118,505,011 (GRCm39) P148S probably damaging Het
Gpsm1 G A 2: 26,209,843 (GRCm39) probably benign Het
Gtpbp2 A G 17: 46,472,239 (GRCm39) Y58C probably damaging Het
Hcrtr2 T A 9: 76,137,838 (GRCm39) T426S probably benign Het
Herc3 T A 6: 58,853,794 (GRCm39) Y613* probably null Het
Hsd17b1 A T 11: 100,970,838 (GRCm39) M265L probably benign Het
Ier3ip1 A G 18: 77,028,294 (GRCm39) probably benign Het
Kif11 A G 19: 37,404,940 (GRCm39) M924V probably benign Het
Kirrel1 C T 3: 86,996,458 (GRCm39) M380I probably null Het
Lancl2 T A 6: 57,690,019 (GRCm39) L75H probably damaging Het
Mfsd4b1 T C 10: 39,888,091 (GRCm39) probably benign Het
Nlrc5 A T 8: 95,247,467 (GRCm39) I1588F probably damaging Het
Nostrin C G 2: 69,006,061 (GRCm39) I248M probably damaging Het
Or14j1 T C 17: 38,146,607 (GRCm39) L239P probably benign Het
Qng1 A G 13: 58,530,239 (GRCm39) L257P probably damaging Het
Rabggta A G 14: 55,953,944 (GRCm39) V266A probably benign Het
Ror2 G A 13: 53,286,016 (GRCm39) T66M possibly damaging Het
Rps6-ps2 A G 8: 89,533,319 (GRCm39) noncoding transcript Het
Skp1 C T 11: 52,135,905 (GRCm39) T138I probably benign Het
Smad9 T C 3: 54,690,182 (GRCm39) V134A probably damaging Het
Snx29 T A 16: 11,238,565 (GRCm39) probably null Het
Sos1 A G 17: 80,761,240 (GRCm39) I152T probably damaging Het
Ssbp2 G A 13: 91,842,175 (GRCm39) G302D probably damaging Het
Stom T C 2: 35,211,545 (GRCm39) N159D possibly damaging Het
Trav16d-dv11 A G 14: 53,285,035 (GRCm39) K37R probably benign Het
Trim75 A G 8: 65,436,369 (GRCm39) V27A probably damaging Het
Ttn T C 2: 76,548,105 (GRCm39) T32066A probably damaging Het
Txndc11 T C 16: 10,893,087 (GRCm39) H881R probably benign Het
Ubp1 C T 9: 113,787,775 (GRCm39) T222I probably benign Het
Unc5cl C G 17: 48,766,833 (GRCm39) P69R possibly damaging Het
Zfp616 T A 11: 73,961,950 (GRCm39) C24S probably damaging Het
Other mutations in Or12d14-ps1
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4468:Or12d14-ps1 UTSW 17 37,673,528 (GRCm39) missense possibly damaging 0.58
R4871:Or12d14-ps1 UTSW 17 37,673,337 (GRCm39) missense probably benign 0.45
R7315:Or12d14-ps1 UTSW 17 37,673,551 (GRCm39) missense probably damaging 0.98
R7568:Or12d14-ps1 UTSW 17 37,673,496 (GRCm39) missense probably benign 0.02
R7982:Or12d14-ps1 UTSW 17 37,673,502 (GRCm39) missense probably damaging 0.99
R8008:Or12d14-ps1 UTSW 17 37,673,265 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TTCCTGGGTAGCACAGAAGC -3'
(R):5'- AAGTGGACAGTGCTTTGTGC -3'

Sequencing Primer
(F):5'- TAGCACAGAAGCCCTGCTG -3'
(R):5'- GCATACTGCAGGAACGAGTCTTC -3'
Posted On 2015-07-21