Incidental Mutation 'R9151:Or5d18'
ID 695010
Institutional Source Beutler Lab
Gene Symbol Or5d18
Ensembl Gene ENSMUSG00000075140
Gene Name olfactory receptor family 5 subfamily D member 18
Synonyms MOR174-9, GA_x6K02T2Q125-49527073-49526132, mOR-EG, Olfr73
MMRRC Submission 068973-MU
Accession Numbers
Essential gene? Possibly essential (E-score: 0.572) question?
Stock # R9151 (G1)
Quality Score 225.009
Status Validated
Chromosome 2
Chromosomal Location 87864540-87865481 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 87864697 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 262 (V262A)
Ref Sequence ENSEMBL: ENSMUSP00000149472 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099838] [ENSMUST00000129056]
AlphaFold Q920P2
Predicted Effect probably damaging
Transcript: ENSMUST00000099838
AA Change: V262A

PolyPhen 2 Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000097426
Gene: ENSMUSG00000075140
AA Change: V262A

DomainStartEndE-ValueType
Pfam:7tm_4 32 309 6e-48 PFAM
Pfam:7tm_1 42 291 6.1e-13 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000129056
AA Change: V262A

PolyPhen 2 Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 100% (71/71)
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: 75 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca5 A G 11: 110,188,908 (GRCm39) F850L probably benign Het
Adam1a A T 5: 121,657,411 (GRCm39) D627E probably damaging Het
Add2 C A 6: 86,081,459 (GRCm39) probably benign Het
Anpep T C 7: 79,491,785 (GRCm39) N72S probably benign Het
Aqp6 A G 15: 99,501,655 (GRCm39) T238A possibly damaging Het
Arhgef38 G T 3: 132,912,706 (GRCm39) T111K Het
Atg10 A G 13: 91,189,032 (GRCm39) Y93H probably damaging Het
Bean1 CT C 8: 104,908,664 (GRCm39) probably null Het
Cald1 A G 6: 34,732,682 (GRCm39) N286S unknown Het
Caps2 A T 10: 112,031,829 (GRCm39) I322F possibly damaging Het
Cbx3 T A 6: 51,455,533 (GRCm39) S95T probably benign Het
Ccdc24 T C 4: 117,727,102 (GRCm39) T83A unknown Het
Cntn1 T C 15: 92,140,864 (GRCm39) Y197H probably damaging Het
Cpd A G 11: 76,675,275 (GRCm39) I1282T possibly damaging Het
Crat A T 2: 30,295,052 (GRCm39) S454R probably damaging Het
D2hgdh G A 1: 93,754,338 (GRCm39) V126I probably benign Het
Dcst1 A G 3: 89,271,558 (GRCm39) V75A probably benign Het
Dnm1l T C 16: 16,176,668 (GRCm39) D21G probably benign Het
Evc2 A G 5: 37,504,823 (GRCm39) N74D probably benign Het
Gm19965 A T 1: 116,748,942 (GRCm39) M208L Het
Gprc6a T G 10: 51,497,182 (GRCm39) T454P possibly damaging Het
Gprin1 C T 13: 54,886,778 (GRCm39) V499M probably benign Het
Gtf3c5 A G 2: 28,463,577 (GRCm39) Y194H probably damaging Het
Hcn4 T C 9: 58,767,880 (GRCm39) V1147A possibly damaging Het
Ighv1-82 A C 12: 115,916,342 (GRCm39) V56G probably damaging Het
Ins2 T C 7: 142,232,505 (GRCm39) D93G possibly damaging Het
Itgb8 A G 12: 119,130,535 (GRCm39) S658P probably benign Het
Kcnmb1 T C 11: 33,920,263 (GRCm39) F159L probably benign Het
Klf1 C T 8: 85,629,954 (GRCm39) L260F probably benign Het
Larp4 T A 15: 99,888,205 (GRCm39) S140T possibly damaging Het
Maneal C A 4: 124,755,542 (GRCm39) R140L probably benign Het
Mfsd11 T A 11: 116,750,323 (GRCm39) V114D Het
Muc4 A G 16: 32,752,617 (GRCm38) T832A probably benign Het
Myh11 T G 16: 14,050,439 (GRCm39) I509L Het
Myh13 A T 11: 67,252,149 (GRCm39) E1419V probably damaging Het
Myh7b A G 2: 155,474,439 (GRCm39) E1718G probably damaging Het
Myo9b T A 8: 71,807,871 (GRCm39) probably benign Het
Notch1 A T 2: 26,367,939 (GRCm39) L656Q probably benign Het
Nova1 A G 12: 46,746,813 (GRCm39) I488T probably damaging Het
Or51r1 A T 7: 102,228,500 (GRCm39) E266V probably damaging Het
Or5b113 A T 19: 13,342,222 (GRCm39) T77S possibly damaging Het
Or5b21 A G 19: 12,839,976 (GRCm39) Y279C probably damaging Het
Or6c35 A G 10: 129,169,623 (GRCm39) N291S probably damaging Het
Or6d13 A T 6: 116,517,990 (GRCm39) N192I possibly damaging Het
Pax6 C T 2: 105,523,097 (GRCm39) S325L probably benign Het
Phldb1 T C 9: 44,619,740 (GRCm39) D142G probably null Het
Phldb3 T G 7: 24,324,048 (GRCm39) probably benign Het
Pikfyve G T 1: 65,235,898 (GRCm39) R190L probably damaging Het
Plagl2 A T 2: 153,074,540 (GRCm39) H120Q probably damaging Het
Pou2f1 A T 1: 165,703,640 (GRCm39) probably benign Het
Pramel58 A G 5: 94,831,836 (GRCm39) Y281C possibly damaging Het
Prpf6 A G 2: 181,250,001 (GRCm39) R54G possibly damaging Het
Prss33 T C 17: 24,052,966 (GRCm39) E236G probably benign Het
Ptpru T C 4: 131,522,278 (GRCm39) Y709C probably benign Het
Rcc1l A G 5: 134,197,057 (GRCm39) V212A probably benign Het
Rtl1 G A 12: 109,560,007 (GRCm39) L611F Het
Scp2 A G 4: 107,931,603 (GRCm39) I344T possibly damaging Het
Serpinb2 A T 1: 107,449,890 (GRCm39) D101V possibly damaging Het
Slc13a1 T C 6: 24,097,662 (GRCm39) T422A probably damaging Het
Slc38a10 G T 11: 120,007,762 (GRCm39) T406K probably benign Het
Smad4 T C 18: 73,782,806 (GRCm39) E376G probably damaging Het
Smarcb1 T C 10: 75,750,916 (GRCm39) E115G probably benign Het
Spata31h1 A T 10: 82,120,928 (GRCm39) H4027Q probably damaging Het
Taf5 G A 19: 47,063,370 (GRCm39) V307I probably damaging Het
Tnc T C 4: 63,938,686 (GRCm39) N51S possibly damaging Het
Trp53inp2 G T 2: 155,228,558 (GRCm39) R171L possibly damaging Het
Ttc13 A T 8: 125,402,021 (GRCm39) D579E probably benign Het
Ttn A T 2: 76,775,896 (GRCm39) N1761K unknown Het
Ttpa C T 4: 20,008,401 (GRCm39) probably benign Het
Ugt3a1 G A 15: 9,362,051 (GRCm39) V276I probably benign Het
Usp4 T A 9: 108,244,011 (GRCm39) H296Q probably benign Het
Vmn1r119 T A 7: 20,745,593 (GRCm39) H263L possibly damaging Het
Vmn2r81 A G 10: 79,103,905 (GRCm39) D176G Het
Wdr1 A T 5: 38,687,468 (GRCm39) probably benign Het
Zfp488 T G 14: 33,692,695 (GRCm39) Q156P possibly damaging Het
Other mutations in Or5d18
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03137:Or5d18 APN 2 87,864,754 (GRCm39) missense probably benign 0.44
IGL03377:Or5d18 APN 2 87,864,589 (GRCm39) missense probably damaging 1.00
PIT4260001:Or5d18 UTSW 2 87,865,126 (GRCm39) missense probably damaging 1.00
R0013:Or5d18 UTSW 2 87,864,610 (GRCm39) missense possibly damaging 0.78
R0969:Or5d18 UTSW 2 87,864,592 (GRCm39) missense probably damaging 0.99
R1216:Or5d18 UTSW 2 87,864,602 (GRCm39) missense probably damaging 0.99
R2148:Or5d18 UTSW 2 87,864,943 (GRCm39) missense probably damaging 0.99
R2355:Or5d18 UTSW 2 87,865,379 (GRCm39) missense probably damaging 0.97
R2357:Or5d18 UTSW 2 87,865,028 (GRCm39) missense probably damaging 1.00
R2994:Or5d18 UTSW 2 87,865,301 (GRCm39) missense probably damaging 1.00
R3806:Or5d18 UTSW 2 87,864,911 (GRCm39) missense possibly damaging 0.60
R4618:Or5d18 UTSW 2 87,864,898 (GRCm39) missense probably benign 0.19
R4975:Or5d18 UTSW 2 87,865,005 (GRCm39) missense probably benign 0.09
R5753:Or5d18 UTSW 2 87,864,920 (GRCm39) missense probably damaging 1.00
R6795:Or5d18 UTSW 2 87,864,668 (GRCm39) missense probably benign 0.02
R8982:Or5d18 UTSW 2 87,864,613 (GRCm39) missense probably damaging 1.00
Z1190:Or5d18 UTSW 2 87,865,007 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- AAACTCAATTTCTACTCTGTTGTGC -3'
(R):5'- TGCCACTTTTAATGAGATTAGCACAC -3'

Sequencing Primer
(F):5'- TGACAAACACAAATGACATAATATGC -3'
(R):5'- GAGATTAGCACACTCCTTATCATTC -3'
Posted On 2022-01-20