Incidental Mutation 'R8786:Or10g3b'
ID 670659
Institutional Source Beutler Lab
Gene Symbol Or10g3b
Ensembl Gene ENSMUSG00000095030
Gene Name olfactory receptor family 10 subfamily G member 3B
Synonyms GA_x6K02T2RJGY-644134-645075, Olfr1513, MOR223-10, MOR223-7P
MMRRC Submission 068632-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.090) question?
Stock # R8786 (G1)
Quality Score 225.009
Status Validated
Chromosome 14
Chromosomal Location 52586560-52587501 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 52587021 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Alanine to Threonine at position 161 (A161T)
Ref Sequence ENSEMBL: ENSMUSP00000149216 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000089739] [ENSMUST00000215147]
AlphaFold L7N457
Predicted Effect possibly damaging
Transcript: ENSMUST00000089739
AA Change: A161T

PolyPhen 2 Score 0.736 (Sensitivity: 0.85; Specificity: 0.92)
SMART Domains Protein: ENSMUSP00000087171
Gene: ENSMUSG00000095030
AA Change: A161T

DomainStartEndE-ValueType
Pfam:7tm_4 31 307 5.2e-49 PFAM
Pfam:7tm_1 41 291 1.6e-20 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000215147
AA Change: A161T

PolyPhen 2 Score 0.736 (Sensitivity: 0.85; Specificity: 0.92)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 100% (72/72)
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: 72 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamtsl4 A T 3: 95,592,784 (GRCm39) M1K probably null Het
Atg2a G T 19: 6,294,460 (GRCm39) V59L probably damaging Het
Atxn7 C A 14: 14,103,316 (GRCm38) T888K possibly damaging Het
Btbd9 T C 17: 30,749,144 (GRCm39) R57G probably damaging Het
Catspere2 T A 1: 177,843,362 (GRCm39) probably benign Het
Catspere2 G A 1: 177,843,555 (GRCm39) probably benign Het
Ccdc9b C A 2: 118,587,732 (GRCm39) S534I unknown Het
Crp T C 1: 172,526,293 (GRCm39) V126A probably benign Het
Csf1r A T 18: 61,247,942 (GRCm39) T337S probably damaging Het
Dcaf12 T C 4: 41,296,439 (GRCm39) N299S probably damaging Het
Dcaf17 T C 2: 70,917,744 (GRCm39) probably null Het
Dip2c A G 13: 9,665,830 (GRCm39) D985G probably damaging Het
Dtna A G 18: 23,716,190 (GRCm39) T138A probably benign Het
Emid1 T C 11: 5,081,517 (GRCm39) D212G probably benign Het
Epyc G A 10: 97,511,525 (GRCm39) D173N probably damaging Het
Fanci A G 7: 79,052,298 (GRCm39) D162G probably benign Het
Firrm A T 1: 163,792,040 (GRCm39) L626Q probably damaging Het
Fry T C 5: 150,317,501 (GRCm39) V827A probably benign Het
Ggps1 T C 13: 14,228,505 (GRCm39) E226G probably benign Het
Gopc G A 10: 52,230,750 (GRCm39) R183* probably null Het
Grik4 C T 9: 42,453,130 (GRCm39) G752S probably damaging Het
H2-D1 T A 17: 35,482,844 (GRCm39) C125S probably damaging Het
H2-Q1 T A 17: 35,539,869 (GRCm39) V46D probably damaging Het
Hsd17b3 T C 13: 64,219,862 (GRCm39) N126S probably damaging Het
Igsf10 G A 3: 59,238,063 (GRCm39) T706I probably benign Het
Kmt2e A G 5: 23,669,864 (GRCm39) D117G probably damaging Het
Kmt5a C T 5: 124,584,074 (GRCm39) A18V probably benign Het
Krtap29-1 C T 11: 99,869,465 (GRCm39) G139R probably damaging Het
Lama5 T C 2: 179,838,100 (GRCm39) Y872C probably damaging Het
Lrriq4 T A 3: 30,704,752 (GRCm39) M260K probably benign Het
Map2 G A 1: 66,472,755 (GRCm39) probably benign Het
Mrpl51 C T 6: 125,169,340 (GRCm39) A8V probably benign Het
Ndufs3 T C 2: 90,732,778 (GRCm39) T103A probably benign Het
Numa1 T G 7: 101,647,616 (GRCm39) L449R probably benign Het
Pan3 C T 5: 147,424,951 (GRCm39) P295S possibly damaging Het
Pds5b T C 5: 150,704,134 (GRCm39) S846P probably damaging Het
Phf2 A T 13: 48,967,219 (GRCm39) M712K unknown Het
Phlda2 A T 7: 143,056,211 (GRCm39) V6E probably benign Het
Pkdrej C A 15: 85,704,044 (GRCm39) A631S probably benign Het
Plcd3 G T 11: 102,962,569 (GRCm39) N627K probably damaging Het
Prpf6 T C 2: 181,262,415 (GRCm39) I138T possibly damaging Het
Psd4 G A 2: 24,295,444 (GRCm39) S866N probably benign Het
Ptprb A C 10: 116,155,306 (GRCm39) T400P probably benign Het
Rxfp1 T C 3: 79,570,677 (GRCm39) probably null Het
Sbf2 A G 7: 110,063,793 (GRCm39) probably null Het
Serpinb9h G A 13: 33,588,204 (GRCm39) R263H probably benign Het
Setd4 C T 16: 93,390,162 (GRCm39) R89Q probably benign Het
Sgpp1 A G 12: 75,763,152 (GRCm39) I343T probably benign Het
Sh2b2 T C 5: 136,260,658 (GRCm39) D186G probably benign Het
Slc12a4 A T 8: 106,680,549 (GRCm39) I191N probably damaging Het
Slc4a4 A T 5: 89,232,549 (GRCm39) D251V probably benign Het
Slc6a5 A T 7: 49,561,843 (GRCm39) D125V possibly damaging Het
Slf1 T A 13: 77,274,806 (GRCm39) I16F possibly damaging Het
Sncaip T C 18: 53,031,334 (GRCm39) V521A probably damaging Het
Spmip10 T C 18: 56,727,568 (GRCm39) F89L probably damaging Het
Stx19 T C 16: 62,642,775 (GRCm39) L197P probably damaging Het
Sucla2 A G 14: 73,797,905 (GRCm39) N39D probably benign Het
Sult1d1 T A 5: 87,712,575 (GRCm39) T90S probably benign Het
Syna C T 5: 134,588,723 (GRCm39) M75I probably benign Het
Tas2r138 A G 6: 40,589,611 (GRCm39) S212P probably damaging Het
Tdrd3 T A 14: 87,709,637 (GRCm39) C106* probably null Het
Tlk2 C T 11: 105,172,059 (GRCm39) A743V unknown Het
Tlr3 T C 8: 45,851,286 (GRCm39) D537G possibly damaging Het
Tmc1 A G 19: 20,803,953 (GRCm39) Y375H probably damaging Het
Tsen54 T A 11: 115,711,498 (GRCm39) M305K probably damaging Het
Umod C T 7: 119,076,581 (GRCm39) V62M possibly damaging Het
Vmn1r10 A G 6: 57,091,010 (GRCm39) T201A probably benign Het
Vmn1r103 T C 7: 20,243,676 (GRCm39) T262A probably benign Het
Vmn2r100 T C 17: 19,742,838 (GRCm39) V404A probably damaging Het
Vmn2r56 A G 7: 12,449,393 (GRCm39) F282L probably damaging Het
Wdr64 A T 1: 175,636,327 (GRCm39) K982* probably null Het
Xpo6 A T 7: 125,712,127 (GRCm39) probably benign Het
Other mutations in Or10g3b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00309:Or10g3b APN 14 52,587,167 (GRCm39) missense probably benign 0.00
IGL02485:Or10g3b APN 14 52,587,501 (GRCm39) start codon destroyed possibly damaging 0.89
IGL02828:Or10g3b APN 14 52,586,799 (GRCm39) missense probably benign 0.02
R0744:Or10g3b UTSW 14 52,586,835 (GRCm39) missense probably benign 0.00
R0833:Or10g3b UTSW 14 52,586,835 (GRCm39) missense probably benign 0.00
R2316:Or10g3b UTSW 14 52,587,395 (GRCm39) missense probably benign 0.00
R4898:Or10g3b UTSW 14 52,586,999 (GRCm39) missense probably damaging 1.00
R5018:Or10g3b UTSW 14 52,586,736 (GRCm39) missense possibly damaging 0.81
R5134:Or10g3b UTSW 14 52,587,248 (GRCm39) missense probably benign 0.03
R5485:Or10g3b UTSW 14 52,586,776 (GRCm39) nonsense probably null
R6819:Or10g3b UTSW 14 52,587,156 (GRCm39) missense probably damaging 1.00
R6877:Or10g3b UTSW 14 52,587,270 (GRCm39) missense possibly damaging 0.95
R7583:Or10g3b UTSW 14 52,587,360 (GRCm39) missense possibly damaging 0.93
R7606:Or10g3b UTSW 14 52,587,420 (GRCm39) missense probably benign 0.33
R7653:Or10g3b UTSW 14 52,586,889 (GRCm39) nonsense probably null
R8111:Or10g3b UTSW 14 52,587,344 (GRCm39) missense possibly damaging 0.70
R8262:Or10g3b UTSW 14 52,586,625 (GRCm39) missense probably damaging 1.00
R8487:Or10g3b UTSW 14 52,586,696 (GRCm39) missense probably damaging 1.00
R9003:Or10g3b UTSW 14 52,586,768 (GRCm39) missense probably damaging 1.00
R9507:Or10g3b UTSW 14 52,586,678 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CTGTGCGGATTCTCAGGATG -3'
(R):5'- ATGCGTGGCTCAGCTTTATTTC -3'

Sequencing Primer
(F):5'- ATTCTCAGGATGGCCCGAATG -3'
(R):5'- CTACCACTTTCTGGGCAGTACTG -3'
Posted On 2021-04-30