Incidental Mutation 'R2483:Or5p81'
ID 250661
Institutional Source Beutler Lab
Gene Symbol Or5p81
Ensembl Gene ENSMUSG00000096209
Gene Name olfactory receptor family 5 subfamily P member 81
Synonyms MOR204-34, GA_x6K02T2PBJ9-10997715-10998659, Olfr510
MMRRC Submission 040407-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.084) question?
Stock # R2483 (G1)
Quality Score 217
Status Not validated
Chromosome 7
Chromosomal Location 108265625-108267569 bp(+) (GRCm39)
Type of Mutation frame shift
DNA Base Change (assembly) CAAATA to CA at 108266869 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000149693 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000076289] [ENSMUST00000213979] [ENSMUST00000216331] [ENSMUST00000217170]
AlphaFold Q8VEW6
Predicted Effect probably null
Transcript: ENSMUST00000076289
SMART Domains Protein: ENSMUSP00000075637
Gene: ENSMUSG00000096209

DomainStartEndE-ValueType
Pfam:7tm_4 34 311 3e-50 PFAM
Pfam:7tm_1 44 293 4e-20 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000210621
Predicted Effect probably null
Transcript: ENSMUST00000213979
Predicted Effect probably null
Transcript: ENSMUST00000216331
Predicted Effect probably null
Transcript: ENSMUST00000217170
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.5%
  • 20x: 95.6%
Validation Efficiency
MGI Phenotype FUNCTION: Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 81 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adcy1 A G 11: 7,080,348 (GRCm39) T364A probably benign Het
Adpgk G A 9: 59,221,036 (GRCm39) V281I probably benign Het
Akap9 C A 5: 4,026,235 (GRCm39) Q1297K possibly damaging Het
Ankrd13d T C 19: 4,331,968 (GRCm39) E110G probably damaging Het
Ankrd53 A G 6: 83,740,244 (GRCm39) E104G possibly damaging Het
Ano6 A T 15: 95,863,855 (GRCm39) T792S probably benign Het
Atm A T 9: 53,421,566 (GRCm39) V715D probably damaging Het
Avl9 A G 6: 56,713,828 (GRCm39) D362G probably benign Het
Bin1 T A 18: 32,547,280 (GRCm39) S152R probably damaging Het
Bscl2 T A 19: 8,818,514 (GRCm39) C40S probably benign Het
Btaf1 A G 19: 36,958,486 (GRCm39) T668A probably benign Het
Btrc A G 19: 45,504,497 (GRCm39) D397G probably damaging Het
Cables2 A T 2: 179,902,222 (GRCm39) V379E probably damaging Het
Cacna2d2 T C 9: 107,389,221 (GRCm39) L228P probably damaging Het
Cd109 A T 9: 78,574,639 (GRCm39) D541V probably damaging Het
Cdh26 A T 2: 178,108,382 (GRCm39) S327C probably damaging Het
Cep78 T C 19: 15,938,344 (GRCm39) K535E probably damaging Het
Ces1a A G 8: 93,753,969 (GRCm39) Y345H probably damaging Het
Col6a5 C A 9: 105,741,347 (GRCm39) R2524I probably damaging Het
Cracd A T 5: 77,004,256 (GRCm39) I206F probably damaging Het
Dctn1 G A 6: 83,171,169 (GRCm39) R661H probably damaging Het
Ddias T C 7: 92,508,800 (GRCm39) T372A probably benign Het
Dffb T C 4: 154,049,976 (GRCm39) T296A probably damaging Het
Dock8 A G 19: 25,057,241 (GRCm39) Q216R probably benign Het
Emx1 T C 6: 85,165,237 (GRCm39) S105P probably benign Het
Ep400 T C 5: 110,867,102 (GRCm39) Y1014C unknown Het
Fam193a A T 5: 34,623,102 (GRCm39) K1230M possibly damaging Het
Fgf9 A G 14: 58,347,028 (GRCm39) Q207R probably benign Het
Gm5460 G A 14: 33,767,775 (GRCm39) C461Y possibly damaging Het
Gpc1 T C 1: 92,783,660 (GRCm39) I249T probably benign Het
Htr1d T C 4: 136,170,815 (GRCm39) I348T probably damaging Het
Hyal4 A T 6: 24,765,737 (GRCm39) S364C probably damaging Het
Igfn1 T C 1: 135,897,275 (GRCm39) E1097G probably benign Het
Igkv1-133 A T 6: 67,701,944 (GRCm39) Q16L probably benign Het
Kcnh5 A T 12: 75,161,245 (GRCm39) I221N probably damaging Het
Kmt2a A G 9: 44,760,263 (GRCm39) Y529H probably damaging Het
Kyat1 T C 2: 30,076,710 (GRCm39) H218R possibly damaging Het
Lamb2 T G 9: 108,357,758 (GRCm39) C94G probably damaging Het
Met A T 6: 17,549,085 (GRCm39) D979V probably damaging Het
Midn A G 10: 79,986,144 (GRCm39) D78G probably benign Het
Myh1 A T 11: 67,102,052 (GRCm39) M811L probably benign Het
Myh7 T C 14: 55,210,838 (GRCm39) E1693G probably damaging Het
Myo15b A G 11: 115,755,565 (GRCm39) T979A probably benign Het
Myo18b A T 5: 113,006,274 (GRCm39) C879S probably damaging Het
Myom1 A G 17: 71,384,807 (GRCm39) T733A probably damaging Het
Ndufa9 A T 6: 126,821,362 (GRCm39) M76K possibly damaging Het
Nectin3 A G 16: 46,215,542 (GRCm39) C74R possibly damaging Het
Obscn A G 11: 58,970,972 (GRCm39) F2514L probably damaging Het
Or4a69 G A 2: 89,313,471 (GRCm39) Q3* probably null Het
Or52d3 T C 7: 104,229,149 (GRCm39) S99P probably damaging Het
P2ry2 A T 7: 100,647,706 (GRCm39) S200T probably benign Het
Pcdha5 G T 18: 37,094,542 (GRCm39) M350I probably benign Het
Pcdha5 G A 18: 37,094,834 (GRCm39) V448M probably damaging Het
Pex12 C T 11: 83,188,455 (GRCm39) R180H possibly damaging Het
Pip4p1 C G 14: 51,167,749 (GRCm39) V59L probably damaging Het
Pkd1l1 A T 11: 8,912,701 (GRCm39) V168E probably damaging Het
Prokr2 T A 2: 132,223,095 (GRCm39) D149V probably damaging Het
Rnf123 A G 9: 107,940,720 (GRCm39) V707A probably benign Het
Ryr2 T C 13: 11,774,589 (GRCm39) E1189G probably damaging Het
Scarf1 T C 11: 75,406,117 (GRCm39) F134L probably damaging Het
Sfxn5 A G 6: 85,309,260 (GRCm39) probably null Het
Shfl A T 9: 20,784,473 (GRCm39) I186F possibly damaging Het
Skic3 A G 13: 76,330,986 (GRCm39) E1472G probably damaging Het
Slc17a5 A T 9: 78,445,556 (GRCm39) V433D probably damaging Het
Snapc1 A G 12: 74,011,417 (GRCm39) T28A probably benign Het
Soat1 T C 1: 156,258,669 (GRCm39) Y528C probably damaging Het
Spem1 G A 11: 69,712,344 (GRCm39) R107C possibly damaging Het
Srcap T C 7: 127,141,319 (GRCm39) S1639P probably damaging Het
Sycp2 A T 2: 178,016,388 (GRCm39) N691K probably damaging Het
Syne2 A T 12: 76,142,311 (GRCm39) I6183F probably damaging Het
Tas2r110 A T 6: 132,845,433 (GRCm39) M155L probably benign Het
Tenm3 G A 8: 48,693,305 (GRCm39) T1859I probably damaging Het
Thsd7b T A 1: 130,030,809 (GRCm39) V1048D probably damaging Het
Vav3 T C 3: 109,248,482 (GRCm39) L43P probably damaging Het
Vmn1r30 A T 6: 58,412,437 (GRCm39) F132I probably benign Het
Vmn2r24 A G 6: 123,792,997 (GRCm39) R775G probably damaging Het
Vps13c T A 9: 67,883,189 (GRCm39) probably null Het
Vps37c T A 19: 10,683,569 (GRCm39) probably null Het
Wwp2 A G 8: 108,275,167 (GRCm39) D388G probably damaging Het
Xirp2 A T 2: 67,355,336 (GRCm39) T3366S probably benign Het
Zbtb49 A C 5: 38,360,701 (GRCm39) probably benign Het
Other mutations in Or5p81
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00909:Or5p81 APN 7 108,266,907 (GRCm39) missense possibly damaging 0.61
IGL00952:Or5p81 APN 7 108,267,445 (GRCm39) missense possibly damaging 0.89
IGL01358:Or5p81 APN 7 108,266,869 (GRCm39) missense possibly damaging 0.90
IGL01663:Or5p81 APN 7 108,267,098 (GRCm39) missense probably benign 0.01
IGL02686:Or5p81 APN 7 108,267,093 (GRCm39) missense probably benign 0.00
PIT4466001:Or5p81 UTSW 7 108,266,743 (GRCm39) missense possibly damaging 0.52
R0095:Or5p81 UTSW 7 108,267,252 (GRCm39) missense probably benign 0.00
R0095:Or5p81 UTSW 7 108,267,252 (GRCm39) missense probably benign 0.00
R0792:Or5p81 UTSW 7 108,267,364 (GRCm39) missense probably damaging 1.00
R0925:Or5p81 UTSW 7 108,267,400 (GRCm39) missense probably benign 0.00
R1829:Or5p81 UTSW 7 108,266,851 (GRCm39) missense probably benign 0.24
R2092:Or5p81 UTSW 7 108,266,869 (GRCm39) frame shift probably null
R3619:Or5p81 UTSW 7 108,267,057 (GRCm39) missense probably benign 0.00
R4386:Or5p81 UTSW 7 108,267,460 (GRCm39) missense probably damaging 0.99
R5298:Or5p81 UTSW 7 108,267,279 (GRCm39) missense probably benign 0.00
R5622:Or5p81 UTSW 7 108,267,289 (GRCm39) missense probably benign
R6079:Or5p81 UTSW 7 108,267,412 (GRCm39) missense probably damaging 0.97
R6138:Or5p81 UTSW 7 108,267,412 (GRCm39) missense probably damaging 0.97
R8359:Or5p81 UTSW 7 108,267,518 (GRCm39) missense probably benign 0.00
R8848:Or5p81 UTSW 7 108,266,929 (GRCm39) missense probably benign 0.03
R8994:Or5p81 UTSW 7 108,267,169 (GRCm39) missense probably damaging 0.96
R9360:Or5p81 UTSW 7 108,266,977 (GRCm39) missense probably damaging 1.00
R9439:Or5p81 UTSW 7 108,266,626 (GRCm39) start codon destroyed probably null 0.97
R9641:Or5p81 UTSW 7 108,267,516 (GRCm39) missense probably damaging 0.98
U15987:Or5p81 UTSW 7 108,267,412 (GRCm39) missense probably damaging 0.97
Z1177:Or5p81 UTSW 7 108,267,043 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GGGCTTAACTGATGACCCAG -3'
(R):5'- TAAGACCCTACAAGCAATTGGATAC -3'

Sequencing Primer
(F):5'- ACTGATGACCCAGTTCTTAGAGTC -3'
(R):5'- CACACTTGTTTGGACATTTTAGTTG -3'
Posted On 2014-12-04