Incidental Mutation 'R4697:Olfr1465'
ID 355806
Institutional Source Beutler Lab
Gene Symbol Olfr1465
Ensembl Gene ENSMUSG00000062199
Gene Name olfactory receptor 1465
Synonyms MOR202-28, GA_x6K02T2RE5P-3645346-3644423
MMRRC Submission 041947-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.115) question?
Stock # R4697 (G1)
Quality Score 225
Status Validated
Chromosome 19
Chromosomal Location 13312768-13315541 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to T at 13313717 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glutamic Acid at position 189 (D189E)
Ref Sequence ENSEMBL: ENSMUSP00000146645 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080142] [ENSMUST00000207340]
AlphaFold Q7TQR2
Predicted Effect probably benign
Transcript: ENSMUST00000080142
AA Change: D189E

PolyPhen 2 Score 0.391 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000079039
Gene: ENSMUSG00000062199
AA Change: D189E

DomainStartEndE-ValueType
Pfam:7tm_4 29 306 7.4e-47 PFAM
Pfam:7tm_1 39 288 3.7e-20 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000207340
AA Change: D189E

PolyPhen 2 Score 0.391 (Sensitivity: 0.90; Specificity: 0.89)
Meta Mutation Damage Score 0.2483 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.5%
Validation Efficiency 96% (75/78)
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: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9030624J02Rik T A 7: 118,791,448 I455N probably damaging Het
A2m T C 6: 121,638,284 M1T probably null Het
Aatf T A 11: 84,449,138 D449V probably damaging Het
Acbd3 T A 1: 180,721,944 probably benign Het
BC005561 A G 5: 104,522,240 K1543E probably benign Het
Bicc1 T A 10: 70,953,484 I366F possibly damaging Het
Ccdc74a T C 16: 17,649,749 S184P possibly damaging Het
Cntn4 T C 6: 106,525,485 V401A probably damaging Het
Cux2 T C 5: 121,873,753 T540A probably damaging Het
Disp2 G T 2: 118,791,684 E966* probably null Het
Dpp7 A G 2: 25,354,919 Y209H probably benign Het
Dstyk T A 1: 132,449,487 F277Y probably damaging Het
Dtx1 A T 5: 120,694,408 probably null Het
Ear-ps2 G A 14: 44,047,060 noncoding transcript Het
Ednra T C 8: 77,664,995 H422R probably benign Het
Erlec1 T A 11: 30,952,640 I67F probably benign Het
Fam161b G A 12: 84,348,558 probably benign Het
Gata5 A T 2: 180,327,379 C345* probably null Het
Glmp T C 3: 88,328,274 V47A probably damaging Het
Gm9762 T A 3: 78,966,550 noncoding transcript Het
Gnas A T 2: 174,298,080 D14V probably damaging Het
Gnl3 T C 14: 31,017,329 S53G probably damaging Het
Grhl3 C T 4: 135,548,466 V527M probably damaging Het
Hoxd10 T A 2: 74,694,187 L281* probably null Het
Kif16b T G 2: 142,690,694 Y1175S probably benign Het
Kif2b A G 11: 91,576,846 S204P probably benign Het
Klhl40 T A 9: 121,778,734 I320N probably damaging Het
Ksr2 G A 5: 117,708,147 R693Q probably damaging Het
Mis12 A G 11: 71,025,326 K62E possibly damaging Het
Mlc1 A G 15: 88,974,777 C102R probably damaging Het
Muc5b T C 7: 141,857,361 I1348T unknown Het
Myh7b A G 2: 155,629,322 E1130G probably damaging Het
Nat8f4 T C 6: 85,901,386 T52A probably benign Het
Nxpe2 C A 9: 48,320,521 V379L probably benign Het
Olfr1231 C A 2: 89,302,902 S230I possibly damaging Het
Olfr1231 T A 2: 89,302,903 S230C probably damaging Het
Olfr1448 C T 19: 12,919,934 C125Y probably damaging Het
Olfr288 G A 15: 98,186,868 R310W probably damaging Het
Pcdhga7 A T 18: 37,717,208 Y756F probably damaging Het
Pcsk6 T A 7: 65,959,241 Y284N probably damaging Het
Pdcd11 T C 19: 47,126,347 V1367A possibly damaging Het
Postn T A 3: 54,375,071 N484K probably damaging Het
Prkd3 C T 17: 78,961,171 V572I probably benign Het
Qser1 T C 2: 104,787,183 S1005G probably benign Het
Radil G T 5: 142,486,801 D951E probably benign Het
Ripk1 C T 13: 34,027,942 R352* probably null Het
Sacs T C 14: 61,212,747 F4081L probably benign Het
Sbf1 A G 15: 89,315,085 V11A possibly damaging Het
Sgip1 T A 4: 102,934,587 F536I probably damaging Het
Slc45a1 A G 4: 150,638,284 L381P probably damaging Het
Smarcad1 C T 6: 65,052,641 P71L probably benign Het
Spns1 T A 7: 126,377,037 D14V probably damaging Het
Sv2c T A 13: 95,986,018 I417F possibly damaging Het
Tas2r113 T A 6: 132,893,516 M169K probably benign Het
Tgm1 A T 14: 55,705,681 N567K probably benign Het
Tln2 C T 9: 67,395,461 R76Q probably damaging Het
Trpm6 T C 19: 18,853,791 V1340A probably benign Het
Tspan18 A T 2: 93,312,030 probably null Het
Txndc11 C T 16: 11,084,314 V679I probably damaging Het
Usf1 G T 1: 171,416,964 G144V possibly damaging Het
Vmn1r59 T C 7: 5,454,452 Y103C probably damaging Het
Vmn2r23 A T 6: 123,741,826 I713F probably damaging Het
Vmn2r79 A T 7: 87,037,960 I850F probably damaging Het
Wdr90 C T 17: 25,855,363 R676H probably benign Het
Zfp867 G A 11: 59,463,661 R281W probably damaging Het
Zfp939 T C 7: 39,472,942 noncoding transcript Het
Other mutations in Olfr1465
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01296:Olfr1465 APN 19 13314126 missense probably damaging 1.00
IGL01548:Olfr1465 APN 19 13313986 missense possibly damaging 0.95
IGL02548:Olfr1465 APN 19 13313938 missense probably damaging 0.98
IGL02663:Olfr1465 APN 19 13313379 missense probably benign 0.01
BB010:Olfr1465 UTSW 19 13314205 missense probably benign
BB020:Olfr1465 UTSW 19 13314205 missense probably benign
PIT4651001:Olfr1465 UTSW 19 13314192 missense probably benign 0.12
R0563:Olfr1465 UTSW 19 13313748 missense probably benign 0.28
R1803:Olfr1465 UTSW 19 13314171 missense possibly damaging 0.90
R2146:Olfr1465 UTSW 19 13314121 missense probably benign 0.23
R4674:Olfr1465 UTSW 19 13313814 missense probably benign 0.17
R4825:Olfr1465 UTSW 19 13314320 splice site probably null
R4884:Olfr1465 UTSW 19 13313670 missense probably benign 0.28
R5647:Olfr1465 UTSW 19 13314189 missense probably damaging 1.00
R6401:Olfr1465 UTSW 19 13313514 missense probably damaging 1.00
R6913:Olfr1465 UTSW 19 13313634 missense probably benign 0.01
R6996:Olfr1465 UTSW 19 13313672 missense probably benign 0.15
R7933:Olfr1465 UTSW 19 13314205 missense probably benign
R8946:Olfr1465 UTSW 19 13314138 missense probably damaging 0.97
R8966:Olfr1465 UTSW 19 13313832 missense probably damaging 1.00
R9641:Olfr1465 UTSW 19 13313736 missense probably damaging 0.98
Predicted Primers PCR Primer
(F):5'- TGCAAATACATGAATATGCCAGTCC -3'
(R):5'- AAGCCCTTGCACTATGCCAC -3'

Sequencing Primer
(F):5'- TACATGAATATGCCAGTCCCATAG -3'
(R):5'- ACCACTATGACTTCAGGTGTG -3'
Posted On 2015-10-21