Incidental Mutation 'R7793:Or3a10'
ID 600065
Institutional Source Beutler Lab
Gene Symbol Or3a10
Ensembl Gene ENSMUSG00000047444
Gene Name olfactory receptor family 3 subfamily A member 10
Synonyms GA_x6K02T2P1NL-4202012-4201065, M5, Olfr139, MOR255-2
MMRRC Submission 045849-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.117) question?
Stock # R7793 (G1)
Quality Score 225.009
Status Validated
Chromosome 11
Chromosomal Location 73935151-73936098 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 73935614 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Leucine at position 162 (H162L)
Ref Sequence ENSEMBL: ENSMUSP00000146141 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000050678] [ENSMUST00000206280] [ENSMUST00000214111]
AlphaFold Q60891
Predicted Effect possibly damaging
Transcript: ENSMUST00000050678
AA Change: H162L

PolyPhen 2 Score 0.893 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000049558
Gene: ENSMUSG00000047444
AA Change: H162L

DomainStartEndE-ValueType
Pfam:7tm_4 34 311 1.4e-56 PFAM
Pfam:7TM_GPCR_Srsx 38 276 5.3e-6 PFAM
Pfam:7tm_1 44 293 8.1e-25 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000206280
AA Change: H162L

PolyPhen 2 Score 0.893 (Sensitivity: 0.82; Specificity: 0.94)
Predicted Effect possibly damaging
Transcript: ENSMUST00000214111
AA Change: H162L

PolyPhen 2 Score 0.893 (Sensitivity: 0.82; Specificity: 0.94)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.8%
Validation Efficiency 100% (94/94)
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: 93 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2200002J24Rik T G 7: 30,399,368 (GRCm39) I54S probably damaging Het
2310002L09Rik C T 4: 73,861,172 (GRCm39) V143M probably benign Het
Abca1 T C 4: 53,042,367 (GRCm39) I1902V not run Het
Apob A C 12: 8,058,124 (GRCm39) D2202A probably damaging Het
Arhgap44 T A 11: 64,900,750 (GRCm39) S623C probably damaging Het
Arhgef7 T A 8: 11,874,507 (GRCm39) W713R possibly damaging Het
Axdnd1 A C 1: 156,166,313 (GRCm39) probably null Het
Bcl9l C A 9: 44,420,994 (GRCm39) H1467N probably damaging Het
Bcl9l T C 9: 44,420,263 (GRCm39) M1223T probably benign Het
Bltp2 C T 11: 78,164,031 (GRCm39) P1124L possibly damaging Het
Brinp3 A G 1: 146,622,306 (GRCm39) N236S probably benign Het
Cckbr T G 7: 105,082,798 (GRCm39) L54V probably benign Het
Cd6 G A 19: 10,775,722 (GRCm39) Q246* probably null Het
Cep89 G A 7: 35,129,353 (GRCm39) R630H probably damaging Het
Ces3a T A 8: 105,782,293 (GRCm39) probably null Het
Cgnl1 T A 9: 71,632,917 (GRCm39) N145Y probably damaging Het
Col6a5 T C 9: 105,775,934 (GRCm39) D1707G probably damaging Het
Cyp2w1 A G 5: 139,341,895 (GRCm39) T103A probably damaging Het
Dip2a A T 10: 76,114,417 (GRCm39) I1021N probably benign Het
Dnah2 T C 11: 69,386,040 (GRCm39) T981A probably benign Het
Dnah8 A G 17: 31,074,918 (GRCm39) I4546V probably benign Het
E2f8 A C 7: 48,527,823 (GRCm39) F106L probably benign Het
Ecpas T C 4: 58,853,150 (GRCm39) N395S probably damaging Het
Eif4g1 G A 16: 20,507,364 (GRCm39) V1413I probably benign Het
Epha10 G A 4: 124,808,246 (GRCm39) V688I probably benign Het
Exoc2 A T 13: 31,095,161 (GRCm39) V245D probably benign Het
Eya4 T A 10: 23,102,714 (GRCm39) E23D probably benign Het
Fbxw10 T A 11: 62,738,213 (GRCm39) W36R possibly damaging Het
Gabbr1 G A 17: 37,358,393 (GRCm39) G44S probably benign Het
Gabrg3 T A 7: 56,829,328 (GRCm39) Q143L probably benign Het
Gm14412 A C 2: 177,007,660 (GRCm39) I78M possibly damaging Het
Gm7298 T C 6: 121,737,563 (GRCm39) probably null Het
Hpse2 A T 19: 43,376,509 (GRCm39) L81Q probably damaging Het
Il18r1 A G 1: 40,510,924 (GRCm39) H3R probably benign Het
Kansl1l T C 1: 66,817,173 (GRCm39) K396E probably damaging Het
Kbtbd3 T A 9: 4,331,221 (GRCm39) S532T probably damaging Het
Lrrtm4 T C 6: 79,999,841 (GRCm39) Y418H probably damaging Het
Mfng G A 15: 78,657,265 (GRCm39) R70C probably damaging Het
Mx2 T A 16: 97,348,083 (GRCm39) I236K probably damaging Het
Mysm1 T C 4: 94,853,369 (GRCm39) Q410R probably damaging Het
Nlrp12 T C 7: 3,294,030 (GRCm39) N100S probably benign Het
Nlrp4b T A 7: 10,459,001 (GRCm39) H773Q probably benign Het
Nlrp5 T A 7: 23,123,343 (GRCm39) S735T possibly damaging Het
Nt5c2 G A 19: 46,880,020 (GRCm39) R363W probably benign Het
Or12k8 A G 2: 36,974,933 (GRCm39) F276L possibly damaging Het
Otud7b A T 3: 96,062,528 (GRCm39) Y589F probably benign Het
P2rx1 T A 11: 72,900,079 (GRCm39) C165* probably null Het
Pax8 T C 2: 24,319,609 (GRCm39) D354G possibly damaging Het
Pdcd11 G A 19: 47,094,871 (GRCm39) V552I probably benign Het
Pde6c G T 19: 38,148,201 (GRCm39) C485F possibly damaging Het
Pex5 T C 6: 124,376,300 (GRCm39) Y434C probably benign Het
Ppargc1a T C 5: 51,619,851 (GRCm39) probably null Het
Prss2 A T 6: 41,501,886 (GRCm39) D224V possibly damaging Het
Psd2 A G 18: 36,136,032 (GRCm39) N440S probably benign Het
Psmb3 T A 11: 97,603,265 (GRCm39) D159E probably benign Het
Ptgr2 T G 12: 84,354,575 (GRCm39) L252R probably damaging Het
Ptpro A T 6: 137,393,818 (GRCm39) N829Y probably damaging Het
Rhobtb2 C A 14: 70,034,280 (GRCm39) R315L probably benign Het
Rimbp2 A T 5: 128,866,759 (GRCm39) V520D possibly damaging Het
Schip1 A T 3: 68,401,911 (GRCm39) Y24F probably benign Het
Sdha A T 13: 74,479,555 (GRCm39) V432E probably damaging Het
Sez6 T C 11: 77,868,426 (GRCm39) L929P probably damaging Het
Shcbp1l A G 1: 153,323,571 (GRCm39) I466V probably benign Het
Skor1 T C 9: 63,052,167 (GRCm39) S601G probably damaging Het
Slc6a7 A C 18: 61,138,851 (GRCm39) L219R probably damaging Het
Smok2a T C 17: 13,444,513 (GRCm39) M30T possibly damaging Het
Sp8 A G 12: 118,813,144 (GRCm39) D333G probably damaging Het
Spp1 G A 5: 104,588,200 (GRCm39) D201N probably damaging Het
Sstr3 A T 15: 78,424,588 (GRCm39) L53Q probably damaging Het
Tacc2 T A 7: 130,224,843 (GRCm39) N509K probably benign Het
Tdrd1 T C 19: 56,852,809 (GRCm39) V1030A probably damaging Het
Tfrc A G 16: 32,437,985 (GRCm39) K346R probably benign Het
Tgm3 G A 2: 129,854,330 (GRCm39) probably null Het
Tomm5 C A 4: 45,106,651 (GRCm39) L88F unknown Het
Trak1 T A 9: 121,245,264 (GRCm39) C46* probably null Het
Trim8 A T 19: 46,504,053 (GRCm39) D535V probably damaging Het
Trpm7 A T 2: 126,665,995 (GRCm39) Y870* probably null Het
Tspoap1 T C 11: 87,655,136 (GRCm39) L286P probably benign Het
Ttll3 AAGTA AAGTAGAGTA 6: 113,376,120 (GRCm39) probably null Het
Ttn T A 2: 76,562,389 (GRCm39) I28819F probably damaging Het
Twf2 T C 9: 106,089,079 (GRCm39) S89P probably damaging Het
Ulk4 C T 9: 121,092,734 (GRCm39) E168K possibly damaging Het
Unc13b T A 4: 43,172,737 (GRCm39) N1188K unknown Het
Utp6 C T 11: 79,828,556 (GRCm39) V528I probably benign Het
Vmn1r78 T C 7: 11,887,241 (GRCm39) F284S probably benign Het
Vmn2r54 T A 7: 12,366,196 (GRCm39) Q246L probably damaging Het
Vmn2r87 A G 10: 130,313,413 (GRCm39) M451T probably benign Het
Vwf C T 6: 125,663,483 (GRCm39) P2808L Het
Wdr97 T C 15: 76,243,307 (GRCm39) L989P Het
Wwc1 T C 11: 35,759,936 (GRCm39) Q693R probably benign Het
Zfp582 C T 7: 6,356,886 (GRCm39) S233L probably damaging Het
Zfp658 T A 7: 43,224,108 (GRCm39) H794Q possibly damaging Het
Zfp882 A G 8: 72,666,985 (GRCm39) D8G probably damaging Het
Other mutations in Or3a10
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0276:Or3a10 UTSW 11 73,935,944 (GRCm39) missense probably damaging 1.00
R0545:Or3a10 UTSW 11 73,935,873 (GRCm39) missense possibly damaging 0.90
R1560:Or3a10 UTSW 11 73,935,441 (GRCm39) missense probably damaging 1.00
R1570:Or3a10 UTSW 11 73,935,633 (GRCm39) missense possibly damaging 0.65
R1781:Or3a10 UTSW 11 73,935,786 (GRCm39) missense probably damaging 1.00
R2002:Or3a10 UTSW 11 73,935,865 (GRCm39) missense possibly damaging 0.49
R2857:Or3a10 UTSW 11 73,935,653 (GRCm39) missense possibly damaging 0.93
R2858:Or3a10 UTSW 11 73,935,653 (GRCm39) missense possibly damaging 0.93
R2859:Or3a10 UTSW 11 73,935,653 (GRCm39) missense possibly damaging 0.93
R3874:Or3a10 UTSW 11 73,935,525 (GRCm39) missense probably damaging 1.00
R5023:Or3a10 UTSW 11 73,935,881 (GRCm39) missense probably damaging 1.00
R5057:Or3a10 UTSW 11 73,935,881 (GRCm39) missense probably damaging 1.00
R5242:Or3a10 UTSW 11 73,935,848 (GRCm39) missense possibly damaging 0.89
R5495:Or3a10 UTSW 11 73,935,611 (GRCm39) missense probably damaging 1.00
R5655:Or3a10 UTSW 11 73,935,160 (GRCm39) nonsense probably null
R7220:Or3a10 UTSW 11 73,935,589 (GRCm39) missense possibly damaging 0.63
R7343:Or3a10 UTSW 11 73,935,726 (GRCm39) missense possibly damaging 0.68
R8169:Or3a10 UTSW 11 73,935,707 (GRCm39) missense possibly damaging 0.95
R8262:Or3a10 UTSW 11 73,935,926 (GRCm39) missense probably damaging 1.00
R8340:Or3a10 UTSW 11 73,935,851 (GRCm39) missense probably damaging 0.96
R8948:Or3a10 UTSW 11 73,935,782 (GRCm39) missense possibly damaging 0.50
R8950:Or3a10 UTSW 11 73,935,782 (GRCm39) missense possibly damaging 0.50
R9046:Or3a10 UTSW 11 73,935,284 (GRCm39) missense probably damaging 1.00
R9202:Or3a10 UTSW 11 73,935,441 (GRCm39) missense probably damaging 1.00
R9575:Or3a10 UTSW 11 73,935,840 (GRCm39) missense probably benign 0.01
R9587:Or3a10 UTSW 11 73,935,360 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- AACGTGGGCATAGGACACTG -3'
(R):5'- ATGAGTGCAGAGTTCCCTACG -3'

Sequencing Primer
(F):5'- GAGATAAGTATCATGGGGACTACTCC -3'
(R):5'- AGAGTTCCCTACGCTGCCTG -3'
Posted On 2019-11-26