Incidental Mutation 'R1237:Olfr101'
Institutional Source Beutler Lab
Gene Symbol Olfr101
Ensembl Gene ENSMUSG00000092077
Gene Nameolfactory receptor 101
SynonymsGA_x6K02T2PSCP-1761617-1760691, MOR250-2
MMRRC Submission 039304-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.079) question?
Stock #R1237 (G1)
Quality Score225
Status Validated
Chromosomal Location37297556-37304313 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 37300265 bp
Amino Acid Change Arginine to Serine at position 52 (R52S)
Ref Sequence ENSEMBL: ENSMUSP00000149851 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000058046] [ENSMUST00000214376] [ENSMUST00000215392]
Predicted Effect probably benign
Transcript: ENSMUST00000058046
AA Change: R52S

PolyPhen 2 Score 0.186 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000061042
Gene: ENSMUSG00000092077
AA Change: R52S

Pfam:7tm_4 29 306 3.3e-53 PFAM
Pfam:7tm_1 39 289 3e-20 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000214376
AA Change: R52S

PolyPhen 2 Score 0.186 (Sensitivity: 0.92; Specificity: 0.87)
Predicted Effect probably benign
Transcript: ENSMUST00000215392
AA Change: R52S

PolyPhen 2 Score 0.186 (Sensitivity: 0.92; Specificity: 0.87)
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.2%
  • 10x: 95.9%
  • 20x: 91.8%
Validation Efficiency 98% (40/41)
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: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcg3 T C 5: 104,948,357 T500A probably damaging Het
Amz1 A T 5: 140,741,284 M1L probably damaging Het
Angptl1 T A 1: 156,858,584 N413K probably damaging Het
Ankrd13b T C 11: 77,474,574 T70A probably damaging Het
Cacna1c C T 6: 118,612,625 R1446H probably damaging Het
Ccdc174 C T 6: 91,890,787 probably benign Het
Ccnc T A 4: 21,730,457 F31L probably benign Het
Celsr1 A C 15: 85,903,974 S2692R probably benign Het
Chd1l C T 3: 97,582,731 E503K probably benign Het
Ddhd1 A T 14: 45,601,650 D65E probably benign Het
Dync1h1 A G 12: 110,665,959 N4504S probably benign Het
Enthd1 A G 15: 80,534,598 S167P probably damaging Het
Fat1 A T 8: 45,044,279 Y4267F probably damaging Het
Hectd4 C T 5: 121,321,507 A813V possibly damaging Het
Ibtk T C 9: 85,720,748 S735G probably benign Het
Itga4 A G 2: 79,279,146 I230V probably null Het
Kcnh8 A T 17: 52,893,960 Q474L probably damaging Het
Kcnh8 G T 17: 52,893,961 Q474H probably damaging Het
Mib1 C T 18: 10,768,149 T466I probably damaging Het
Olfr1368 C T 13: 21,142,167 V297I probably benign Het
Olfr167 A C 16: 19,515,625 Y4D probably benign Het
Parp14 G A 16: 35,856,760 A946V probably benign Het
Prdx6b A G 2: 80,293,176 I110V probably benign Het
Prf1 A C 10: 61,303,649 D462A probably benign Het
Rps6ka5 T C 12: 100,575,705 D391G possibly damaging Het
Scn7a A T 2: 66,680,295 N1254K probably damaging Het
Skor2 A T 18: 76,876,132 K924* probably null Het
Slc22a21 A G 11: 53,979,772 I29T probably benign Het
Tas2r140 T C 6: 133,055,208 T196A probably benign Het
Thrap3 A G 4: 126,180,069 S295P probably benign Het
Ubtd2 C T 11: 32,516,125 R115W probably damaging Het
Unc93b1 A G 19: 3,935,228 E12G possibly damaging Het
Vgll3 T A 16: 65,839,573 Y203* probably null Het
Vmn1r212 G A 13: 22,883,468 Q232* probably null Het
Vmn2r107 T A 17: 20,356,685 L315* probably null Het
Vmn2r84 T A 10: 130,387,856 probably null Het
Washc5 A G 15: 59,338,908 probably benign Het
Other mutations in Olfr101
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01583:Olfr101 APN 17 37299738 missense probably benign 0.00
IGL01584:Olfr101 APN 17 37299738 missense probably benign 0.00
IGL01609:Olfr101 APN 17 37299738 missense probably benign 0.00
IGL01739:Olfr101 APN 17 37299782 missense probably benign 0.00
IGL03203:Olfr101 APN 17 37300426 splice site probably benign
R1122:Olfr101 UTSW 17 37300128 missense probably damaging 1.00
R1132:Olfr101 UTSW 17 37299532 missense probably benign 0.19
R3423:Olfr101 UTSW 17 37299870 missense probably benign 0.00
R3872:Olfr101 UTSW 17 37299979 missense probably benign 0.00
R3873:Olfr101 UTSW 17 37299979 missense probably benign 0.00
R3874:Olfr101 UTSW 17 37299979 missense probably benign 0.00
R4871:Olfr101 UTSW 17 37300204 missense probably benign 0.03
R5213:Olfr101 UTSW 17 37300051 missense probably damaging 0.98
R5974:Olfr101 UTSW 17 37300338 missense possibly damaging 0.65
R6294:Olfr101 UTSW 17 37299553 missense probably benign 0.02
Predicted Primers PCR Primer

Sequencing Primer
Posted On2014-01-29