Incidental Mutation 'R6373:Olfr1165-ps'
ID 513615
Institutional Source Beutler Lab
Gene Symbol Olfr1165-ps
Ensembl Gene ENSMUSG00000046590
Gene Name olfactory receptor 1165, pseudogene
Synonyms GA_x6K02T2Q125-49593880-49592930, MOR174-7
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.081) question?
Stock # R6373 (G1)
Quality Score 225.009
Status Not validated
Chromosome 2
Chromosomal Location 88101036-88101985 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to C at 88101845 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Methionine at position 47 (I47M)
Ref Sequence ENSEMBL: ENSMUSP00000149054 (fasta)
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000117860
AA Change: I47M

PolyPhen 2 Score 0.730 (Sensitivity: 0.86; Specificity: 0.92)
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.3%
  • 20x: 95.2%
Validation Efficiency 95% (37/39)
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abhd13 T C 8: 9,988,240 L279P probably damaging Het
Aldh16a1 C G 7: 45,146,271 V373L probably benign Het
Btn2a2 T C 13: 23,481,829 K278E probably benign Het
Carns1 G T 19: 4,166,516 Q556K probably benign Het
Chd1 A T 17: 15,738,636 E650V probably damaging Het
Cobl A G 11: 12,253,118 S1195P probably damaging Het
Ddx58 A G 4: 40,216,487 Y504H possibly damaging Het
Deup1 T C 9: 15,561,342 H464R probably damaging Het
Eva1a T C 6: 82,091,866 L58S probably damaging Het
Fign A C 2: 63,979,645 M427R probably benign Het
Gm6309 A T 5: 146,170,275 I87N probably damaging Het
Gm7879 A G 5: 43,913,551 T127A probably damaging Het
Helz A G 11: 107,595,184 T140A probably benign Het
Helz2 C T 2: 181,233,467 E1745K probably damaging Het
Hist1h2ad A G 13: 23,574,853 K128R probably benign Het
Kif16b A T 2: 142,699,698 H1227Q possibly damaging Het
Mab21l1 A T 3: 55,783,084 I31F possibly damaging Het
Mex3c T C 18: 73,589,994 M386T probably benign Het
Myh11 T A 16: 14,205,130 I1644F possibly damaging Het
Nav2 C T 7: 49,453,175 P513S probably damaging Het
Ncoa3 C T 2: 166,059,347 S953F possibly damaging Het
Nmt2 A G 2: 3,324,951 T462A probably benign Het
Nrxn2 T C 19: 6,509,830 I163T probably damaging Het
Nrxn3 G C 12: 89,976,469 G122R probably damaging Het
Olfr385 A G 11: 73,588,898 V280A probably benign Het
Parg T G 14: 32,209,497 probably null Het
Pcdhb7 T A 18: 37,342,211 C133* probably null Het
Rpe T C 1: 66,715,980 F174L probably benign Het
Rxrb A G 17: 34,033,559 N40S probably benign Het
Ryr3 C A 2: 112,656,544 G3840W probably damaging Het
Smurf2 A G 11: 106,833,769 L529P probably damaging Het
Sntg2 C T 12: 30,258,041 R215H probably benign Het
Spata20 A G 11: 94,483,400 V348A probably benign Het
Spink5 A G 18: 43,990,672 E342G probably damaging Het
St3gal1 A G 15: 67,111,346 V187A possibly damaging Het
Syce1l T A 8: 113,649,511 M31K probably benign Het
Ttn C T 2: 76,788,616 V14394I probably damaging Het
Twnk G A 19: 45,009,381 V450M probably damaging Het
Vangl1 T C 3: 102,158,448 K407R probably benign Het
Vmn1r19 T C 6: 57,405,332 I290T unknown Het
Other mutations in Olfr1165-ps
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4378:Olfr1165-ps UTSW 2 88101485 missense unknown
R5078:Olfr1165-ps UTSW 2 88101535 missense probably benign 0.03
R6698:Olfr1165-ps UTSW 2 88101217 missense unknown
R6736:Olfr1165-ps UTSW 2 88101603 missense probably benign 0.03
R7164:Olfr1165-ps UTSW 2 88101832 missense probably damaging 0.97
R7285:Olfr1165-ps UTSW 2 88101705 missense probably damaging 1.00
R7807:Olfr1165-ps UTSW 2 88101565 missense probably benign 0.00
R8040:Olfr1165-ps UTSW 2 88101359 missense unknown
R8509:Olfr1165-ps UTSW 2 88101522 missense probably benign 0.16
R9047:Olfr1165-ps UTSW 2 88101072 missense unknown
Predicted Primers
Posted On 2018-04-27