Incidental Mutation 'R4008:Olfr192'
ID475055
Institutional Source Beutler Lab
Gene Symbol Olfr192
Ensembl Gene ENSMUSG00000059041
Gene Nameolfactory receptor 192
SynonymsMOR183-11_p, GA_x54KRFPKG5P-55327126-55326203
MMRRC Submission 040946-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.140) question?
Stock #R4008 (G1)
Quality Score225
Status Not validated
Chromosome16
Chromosomal Location59098066-59098990 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to A at 59098761 bp
ZygosityHeterozygous
Amino Acid Change Threonine to Isoleucine at position 77 (T77I)
Ref Sequence ENSEMBL: ENSMUSP00000145941 (fasta)
Predicted Effect unknown
Transcript: ENSMUST00000080251
AA Change: T77I
Predicted Effect unknown
Transcript: ENSMUST00000205727
AA Change: T77I
Predicted Effect unknown
Transcript: ENSMUST00000206214
AA Change: T77I
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 96.9%
  • 20x: 93.8%
Validation Efficiency 97% (32/33)
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acss2 T A 2: 155,557,628 L529Q probably damaging Het
Adsl T C 15: 80,966,156 S359P probably benign Het
Batf2 G A 19: 6,171,348 E63K probably damaging Het
Chd1l A T 3: 97,570,402 M679K probably benign Het
Clvs2 G A 10: 33,543,462 H199Y probably damaging Het
F830045P16Rik A T 2: 129,463,547 N302K probably damaging Het
H2-K1 G A 17: 33,999,551 probably benign Het
Ifit2 G T 19: 34,574,045 M328I probably benign Het
Larp7 T C 3: 127,540,870 D490G probably benign Het
Map9 T C 3: 82,359,083 Y12H probably damaging Het
Mn1 G T 5: 111,420,169 E668D probably benign Het
Mrps18c T C 5: 100,803,116 probably benign Het
Npdc1 T A 2: 25,408,980 Y237* probably null Het
Olfr1122 A T 2: 87,388,580 I292F possibly damaging Het
Olfr722 A G 14: 49,895,007 L265P probably benign Het
Oprm1 A G 10: 6,832,520 M388V probably benign Het
Pkn2 T C 3: 142,810,458 D568G possibly damaging Het
Pwp1 A G 10: 85,882,034 T279A possibly damaging Het
Rabep2 C A 7: 126,445,374 D547E probably damaging Het
Rbm34 T C 8: 126,949,287 K426R probably benign Het
Rgs14 T G 13: 55,369,913 L8V probably damaging Het
Ripor2 A G 13: 24,696,538 H407R probably benign Het
Serpina3a A T 12: 104,118,643 D99V probably benign Het
Shroom3 G T 5: 92,943,086 V1151F probably damaging Het
Slc39a12 T C 2: 14,452,117 F603L probably damaging Het
Smg5 T C 3: 88,349,158 S244P probably benign Het
St3gal3 T C 4: 117,940,440 I252V probably benign Het
Tarsl2 T A 7: 65,678,128 D528E probably damaging Het
Try10 A G 6: 41,356,674 T118A probably benign Het
Tshr C T 12: 91,537,494 S402L probably benign Het
Other mutations in Olfr192
AlleleSourceChrCoordTypePredicted EffectPPH Score
R3807:Olfr192 UTSW 16 59098843 makesense probably null
R3872:Olfr192 UTSW 16 59098761 missense unknown
R4009:Olfr192 UTSW 16 59098761 missense unknown
R4011:Olfr192 UTSW 16 59098761 missense unknown
R4043:Olfr192 UTSW 16 59098761 missense unknown
R4044:Olfr192 UTSW 16 59098761 missense unknown
R4296:Olfr192 UTSW 16 59098761 missense unknown
R4300:Olfr192 UTSW 16 59098278 missense unknown
R4948:Olfr192 UTSW 16 59098977 missense probably damaging 0.99
R5411:Olfr192 UTSW 16 59098704 missense unknown
R5426:Olfr192 UTSW 16 59098302 missense possibly damaging 0.93
R5436:Olfr192 UTSW 16 59098819 missense unknown
R5597:Olfr192 UTSW 16 59098347 missense unknown
R6758:Olfr192 UTSW 16 59098965 missense probably damaging 0.96
R6882:Olfr192 UTSW 16 59098627 missense unknown
Predicted Primers
Posted On2017-04-14