Incidental Mutation 'R7157:Or10a3'
ID 557375
Institutional Source Beutler Lab
Gene Symbol Or10a3
Ensembl Gene ENSMUSG00000046431
Gene Name olfactory receptor family 10 subfamily A member 3
Synonyms Olfr518, MOR268-5, GA_x6K02T2PBJ9-11211854-11210853
MMRRC Submission 045258-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.165) question?
Stock # R7157 (G1)
Quality Score 225.009
Status Not validated
Chromosome 7
Chromosomal Location 108479810-108480811 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 108480475 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Leucine at position 113 (F113L)
Ref Sequence ENSEMBL: ENSMUSP00000151883 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000059617] [ENSMUST00000217803]
AlphaFold Q8VEW1
Predicted Effect probably benign
Transcript: ENSMUST00000059617
AA Change: F113L

PolyPhen 2 Score 0.026 (Sensitivity: 0.95; Specificity: 0.81)
SMART Domains Protein: ENSMUSP00000050503
Gene: ENSMUSG00000046431
AA Change: F113L

DomainStartEndE-ValueType
low complexity region 11 22 N/A INTRINSIC
Pfam:7tm_4 50 327 7.1e-60 PFAM
Pfam:7tm_1 60 318 1.4e-23 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000217803
AA Change: F113L

PolyPhen 2 Score 0.026 (Sensitivity: 0.95; Specificity: 0.81)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.2%
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: 65 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2610021A01Rik G A 7: 41,276,400 (GRCm39) G701D probably damaging Het
6030468B19Rik T A 11: 117,693,780 (GRCm39) N82K probably damaging Het
Abca17 A T 17: 24,554,564 (GRCm39) V130E possibly damaging Het
Alpk2 T A 18: 65,399,348 (GRCm39) K2077* probably null Het
Aox1 T C 1: 58,322,651 (GRCm39) F73S probably benign Het
Ap3b1 T A 13: 94,668,542 (GRCm39) C965* probably null Het
Arhgef10 T A 8: 14,980,030 (GRCm39) V90E probably damaging Het
Atr T A 9: 95,751,953 (GRCm39) H523Q probably benign Het
Bicdl1 G T 5: 115,789,916 (GRCm39) Q511K possibly damaging Het
Capn15 A T 17: 26,184,228 (GRCm39) N150K probably damaging Het
Card6 A T 15: 5,129,591 (GRCm39) W602R probably benign Het
Clnk A T 5: 38,927,234 (GRCm39) S82T possibly damaging Het
Cmah T C 13: 24,620,612 (GRCm39) I282T probably damaging Het
Cog8 A G 8: 107,779,131 (GRCm39) I382T probably benign Het
Dhrs7c G T 11: 67,700,722 (GRCm39) probably null Het
Dhrs9 T A 2: 69,223,502 (GRCm39) D83E probably damaging Het
Dmac2l A T 12: 69,788,562 (GRCm39) N154Y probably benign Het
Dmgdh G A 13: 93,852,043 (GRCm39) G624E probably damaging Het
Dnajc30 C A 5: 135,093,569 (GRCm39) F155L probably damaging Het
Drc7 A C 8: 95,800,778 (GRCm39) K600T probably damaging Het
Efhb A C 17: 53,707,928 (GRCm39) I745S probably damaging Het
Elp1 ACTTCTTCTTCTTCTTCTTCTTC ACTTCTTCTTCTTCTTCTTC 4: 56,781,176 (GRCm39) probably benign Het
Fasn T A 11: 120,701,291 (GRCm39) K1988* probably null Het
Gad2 T C 2: 22,525,035 (GRCm39) L273P probably damaging Het
Gm45861 A T 8: 28,032,536 (GRCm39) K887* probably null Het
Gm45861 A T 8: 28,032,537 (GRCm39) K887I unknown Het
Gm9195 A G 14: 72,718,221 (GRCm39) Y152H probably damaging Het
Grip1 G A 10: 119,781,061 (GRCm39) D237N probably damaging Het
Hamp A C 7: 30,641,961 (GRCm39) C65G possibly damaging Het
Hes3 A G 4: 152,372,581 (GRCm39) probably benign Het
Hgh1 T C 15: 76,254,650 (GRCm39) I342T probably damaging Het
Hlcs T A 16: 94,069,023 (GRCm39) K66* probably null Het
Ift80 A T 3: 68,898,277 (GRCm39) C19* probably null Het
Kbtbd12 C T 6: 88,595,650 (GRCm39) C60Y probably damaging Het
Kdm4c T A 4: 74,263,804 (GRCm39) V696E probably benign Het
Lect2 A G 13: 56,690,803 (GRCm39) I117T unknown Het
Lipn T A 19: 34,054,390 (GRCm39) Y209* probably null Het
Lpin3 G A 2: 160,740,627 (GRCm39) V391I probably benign Het
Mocs2 A T 13: 114,961,143 (GRCm39) I47L probably benign Het
Mogs T A 6: 83,095,488 (GRCm39) H768Q probably benign Het
Nbeal1 T A 1: 60,276,317 (GRCm39) I686N probably damaging Het
Nbeal1 T A 1: 60,299,793 (GRCm39) C1376* probably null Het
Ninl A G 2: 150,791,263 (GRCm39) Y1087H possibly damaging Het
Or10ak14 A G 4: 118,611,615 (GRCm39) V42A possibly damaging Het
Or4k5 A G 14: 50,385,689 (GRCm39) L214S probably damaging Het
Or51b6b A C 7: 103,309,788 (GRCm39) L223R probably damaging Het
Or6s1 A G 14: 51,308,616 (GRCm39) V78A possibly damaging Het
Or8k30 T A 2: 86,339,369 (GRCm39) C189S probably damaging Het
Pkn1 A G 8: 84,398,363 (GRCm39) F768S probably damaging Het
Plekha2 A G 8: 25,553,957 (GRCm39) F82L probably damaging Het
Ppie T C 4: 123,028,900 (GRCm39) E111G probably benign Het
Rps6ka5 T C 12: 100,547,679 (GRCm39) Y277C probably damaging Het
Scgb2b12 A G 7: 32,026,102 (GRCm39) V30A probably benign Het
Serac1 A T 17: 6,124,476 (GRCm39) S16T probably benign Het
Sf3a3 T C 4: 124,616,693 (GRCm39) Y192H probably damaging Het
Slc14a1 A G 18: 78,145,626 (GRCm39) V436A probably benign Het
Smc3 T A 19: 53,630,329 (GRCm39) M1112K probably damaging Het
Tnk2 G A 16: 32,499,986 (GRCm39) G1017E probably damaging Het
Tnn T A 1: 159,953,947 (GRCm39) K603* probably null Het
Trpm6 T C 19: 18,815,462 (GRCm39) S1183P possibly damaging Het
Ttn A T 2: 76,614,724 (GRCm39) V16964E possibly damaging Het
Usp17le G A 7: 104,417,696 (GRCm39) T482I probably benign Het
Vmn1r219 T A 13: 23,347,525 (GRCm39) M238K probably damaging Het
Wfs1 C T 5: 37,124,516 (GRCm39) G792S probably benign Het
Xpa A T 4: 46,185,612 (GRCm39) L122Q probably damaging Het
Other mutations in Or10a3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02713:Or10a3 APN 7 108,480,060 (GRCm39) missense probably damaging 0.99
IGL02995:Or10a3 APN 7 108,480,198 (GRCm39) missense probably damaging 1.00
IGL03162:Or10a3 APN 7 108,480,811 (GRCm39) start codon destroyed probably null
IGL03389:Or10a3 APN 7 108,479,982 (GRCm39) missense probably damaging 0.99
R0731:Or10a3 UTSW 7 108,480,740 (GRCm39) missense probably damaging 1.00
R1669:Or10a3 UTSW 7 108,479,920 (GRCm39) missense probably benign 0.00
R2235:Or10a3 UTSW 7 108,480,172 (GRCm39) missense probably benign 0.09
R4740:Or10a3 UTSW 7 108,480,689 (GRCm39) missense probably benign 0.05
R4902:Or10a3 UTSW 7 108,480,624 (GRCm39) missense probably benign 0.00
R5343:Or10a3 UTSW 7 108,480,205 (GRCm39) missense possibly damaging 0.87
R6744:Or10a3 UTSW 7 108,480,037 (GRCm39) missense probably damaging 0.99
R7326:Or10a3 UTSW 7 108,480,023 (GRCm39) missense probably damaging 1.00
R7713:Or10a3 UTSW 7 108,479,889 (GRCm39) missense probably damaging 1.00
R7819:Or10a3 UTSW 7 108,480,610 (GRCm39) missense probably damaging 0.99
R7939:Or10a3 UTSW 7 108,480,481 (GRCm39) missense probably benign 0.05
R8057:Or10a3 UTSW 7 108,480,571 (GRCm39) missense probably damaging 1.00
R8096:Or10a3 UTSW 7 108,480,248 (GRCm39) nonsense probably null
R8472:Or10a3 UTSW 7 108,479,973 (GRCm39) missense possibly damaging 0.95
R8766:Or10a3 UTSW 7 108,480,453 (GRCm39) missense probably benign 0.05
R9283:Or10a3 UTSW 7 108,480,289 (GRCm39) missense probably benign 0.03
R9570:Or10a3 UTSW 7 108,480,504 (GRCm39) missense possibly damaging 0.95
R9763:Or10a3 UTSW 7 108,480,874 (GRCm39) start gained probably benign
X0066:Or10a3 UTSW 7 108,480,679 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- GCACAGTAGCCACCATGATC -3'
(R):5'- ACTCCAAGGGCAGATGTTTGG -3'

Sequencing Primer
(F):5'- CATGATCCCAGATACCCATGAG -3'
(R):5'- CCTGGTAATTTATCTGGTGACCCTG -3'
Posted On 2019-06-26