Incidental Mutation 'R4695:Or5p72'
ID 355625
Institutional Source Beutler Lab
Gene Symbol Or5p72
Ensembl Gene ENSMUSG00000095239
Gene Name olfactory receptor family 5 subfamily P member 72
Synonyms MOR204-9, GA_x6K02T2PBJ9-10752603-10753547, Olfr497
MMRRC Submission 042016-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.065) question?
Stock # R4695 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 108021780-108022724 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 108022196 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Isoleucine at position 139 (M139I)
Ref Sequence ENSEMBL: ENSMUSP00000150439 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000076406] [ENSMUST00000213521]
AlphaFold Q8VG08
Predicted Effect probably benign
Transcript: ENSMUST00000076406
AA Change: M139I

PolyPhen 2 Score 0.177 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000075741
Gene: ENSMUSG00000095239
AA Change: M139I

DomainStartEndE-ValueType
Pfam:7tm_4 34 311 5.5e-55 PFAM
Pfam:7tm_1 44 293 1.4e-20 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000208862
Predicted Effect noncoding transcript
Transcript: ENSMUST00000211454
AA Change: M139I
Predicted Effect probably benign
Transcript: ENSMUST00000213521
AA Change: M139I

PolyPhen 2 Score 0.177 (Sensitivity: 0.92; Specificity: 0.87)
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.1%
  • 20x: 95.0%
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: 68 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts10 T A 17: 33,750,713 (GRCm39) M251K possibly damaging Het
Adcy2 A T 13: 68,875,962 (GRCm39) H513Q possibly damaging Het
Afg2a T G 3: 37,512,474 (GRCm39) F713C probably damaging Het
Ahctf1 A G 1: 179,580,619 (GRCm39) L1861P possibly damaging Het
Apc2 C A 10: 80,146,877 (GRCm39) R615S probably damaging Het
Arhgap45 A C 10: 79,861,364 (GRCm39) D509A probably damaging Het
Atp6v1c2 T C 12: 17,351,208 (GRCm39) T108A probably benign Het
Blm T A 7: 80,143,976 (GRCm39) D821V probably damaging Het
C3 T A 17: 57,528,057 (GRCm39) I721L probably benign Het
Ccdc13 A T 9: 121,649,826 (GRCm39) V207E probably damaging Het
Ccndbp1 C T 2: 120,845,208 (GRCm39) probably benign Het
Cd180 A C 13: 102,842,268 (GRCm39) Q438P probably benign Het
Cd248 C T 19: 5,118,473 (GRCm39) T107M probably damaging Het
Cdan1 G A 2: 120,558,864 (GRCm39) R445C probably damaging Het
Cic C A 7: 24,973,013 (GRCm39) H915N possibly damaging Het
Cox8c T C 12: 102,865,742 (GRCm39) S40P possibly damaging Het
Cyp2d34 A T 15: 82,501,092 (GRCm39) C347S probably benign Het
Dhx30 A T 9: 109,914,356 (GRCm39) F974I probably damaging Het
Dlec1 A T 9: 118,972,221 (GRCm39) T1414S probably benign Het
Dlg2 C A 7: 92,087,170 (GRCm39) probably null Het
Dynlt5 T A 4: 102,861,426 (GRCm39) I136K probably damaging Het
Dzip1l T A 9: 99,529,258 (GRCm39) M329K probably benign Het
Dzip3 A T 16: 48,771,924 (GRCm39) L582I probably damaging Het
Emilin2 T C 17: 71,559,773 (GRCm39) Y1068C probably damaging Het
Fam221b T A 4: 43,659,622 (GRCm39) probably null Het
Fbxw22 A G 9: 109,207,939 (GRCm39) I444T probably damaging Het
Flnc T A 6: 29,440,428 (GRCm39) N245K probably damaging Het
Fnip1 T A 11: 54,390,245 (GRCm39) I380N probably damaging Het
Gbf1 C T 19: 46,247,606 (GRCm39) R181* probably null Het
Igkv6-17 T A 6: 70,348,486 (GRCm39) F12I probably benign Het
Itln1 C A 1: 171,358,645 (GRCm39) G174V probably damaging Het
Lrrc52 A G 1: 167,293,660 (GRCm39) probably null Het
LTO1 T C 7: 144,482,715 (GRCm39) probably null Het
Matn2 A G 15: 34,403,071 (GRCm39) Y432C probably damaging Het
Metap1d A G 2: 71,355,305 (GRCm39) *336W probably null Het
Mgam2-ps T A 6: 40,779,489 (GRCm39) noncoding transcript Het
Mrps9 T A 1: 42,901,675 (GRCm39) V61D possibly damaging Het
Myh7b T C 2: 155,456,097 (GRCm39) Y161H probably damaging Het
Myh9 T A 15: 77,653,053 (GRCm39) D1428V probably damaging Het
N4bp3 A T 11: 51,535,306 (GRCm39) probably null Het
Nat9 T A 11: 115,075,416 (GRCm39) Q75L probably benign Het
Nop2 T C 6: 125,121,519 (GRCm39) V767A probably benign Het
Ntrk2 A G 13: 59,274,307 (GRCm39) K728E probably damaging Het
Or51e1 T G 7: 102,358,764 (GRCm39) C99W probably damaging Het
Or7g21 T A 9: 19,032,306 (GRCm39) H15Q probably null Het
Pcdhgb2 A G 18: 37,825,375 (GRCm39) T789A probably benign Het
Pcyt2 T C 11: 120,502,000 (GRCm39) D321G probably benign Het
Rad9a G A 19: 4,250,560 (GRCm39) R85C probably damaging Het
Rbbp8 A T 18: 11,854,839 (GRCm39) K355* probably null Het
Rhag T C 17: 41,147,358 (GRCm39) Y407H probably damaging Het
Robo4 G A 9: 37,314,495 (GRCm39) V161M probably damaging Het
Rpl27-ps3 C A 18: 6,332,922 (GRCm39) N97K probably benign Het
Slc45a4 A G 15: 73,453,924 (GRCm39) I691T possibly damaging Het
Slc9a9 A T 9: 94,818,502 (GRCm39) probably benign Het
Stard13 A G 5: 150,984,280 (GRCm39) F619L probably benign Het
Stt3b A T 9: 115,083,862 (GRCm39) V438E probably damaging Het
Tacr3 C T 3: 134,535,182 (GRCm39) T50I probably benign Het
Tacr3 G T 3: 134,635,690 (GRCm39) C298F probably damaging Het
Taok3 C T 5: 117,366,131 (GRCm39) T394M probably benign Het
Tgfb1i1 A G 7: 127,848,348 (GRCm39) D128G probably damaging Het
Tgfbr3l G T 8: 4,300,574 (GRCm39) V251L probably benign Het
Tom1l2 C G 11: 60,161,259 (GRCm39) R84P probably damaging Het
Top3a A G 11: 60,633,238 (GRCm39) S953P probably benign Het
Trappc10 T C 10: 78,033,697 (GRCm39) K957E probably damaging Het
Ttn T A 2: 76,565,668 (GRCm39) E28228V probably damaging Het
Ttn T A 2: 76,585,168 (GRCm39) I22042F probably damaging Het
Vdr A T 15: 97,756,801 (GRCm39) probably null Het
Zfp42 A T 8: 43,749,168 (GRCm39) L111Q probably damaging Het
Other mutations in Or5p72
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01448:Or5p72 APN 7 108,022,235 (GRCm39) nonsense probably null
IGL03145:Or5p72 APN 7 108,021,806 (GRCm39) missense probably benign 0.00
R0732:Or5p72 UTSW 7 108,021,784 (GRCm39) missense probably benign 0.00
R1892:Or5p72 UTSW 7 108,022,147 (GRCm39) missense possibly damaging 0.61
R2008:Or5p72 UTSW 7 108,022,389 (GRCm39) missense probably benign 0.01
R3721:Or5p72 UTSW 7 108,022,326 (GRCm39) missense probably damaging 1.00
R4497:Or5p72 UTSW 7 108,022,122 (GRCm39) missense probably benign 0.37
R4674:Or5p72 UTSW 7 108,022,309 (GRCm39) missense possibly damaging 0.65
R4675:Or5p72 UTSW 7 108,022,309 (GRCm39) missense possibly damaging 0.65
R5265:Or5p72 UTSW 7 108,022,609 (GRCm39) missense possibly damaging 0.94
R5656:Or5p72 UTSW 7 108,021,825 (GRCm39) missense probably benign 0.03
R5758:Or5p72 UTSW 7 108,022,369 (GRCm39) missense probably benign 0.02
R6124:Or5p72 UTSW 7 108,022,725 (GRCm39) splice site probably null
R6787:Or5p72 UTSW 7 108,021,889 (GRCm39) missense possibly damaging 0.52
R7174:Or5p72 UTSW 7 108,022,367 (GRCm39) missense probably benign 0.01
R7222:Or5p72 UTSW 7 108,021,844 (GRCm39) missense probably benign 0.00
R7240:Or5p72 UTSW 7 108,022,140 (GRCm39) missense probably damaging 1.00
R8752:Or5p72 UTSW 7 108,022,480 (GRCm39) missense probably benign
R9548:Or5p72 UTSW 7 108,022,416 (GRCm39) missense possibly damaging 0.75
R9786:Or5p72 UTSW 7 108,021,924 (GRCm39) missense probably benign 0.28
Predicted Primers PCR Primer
(F):5'- ACATGGGCCTTTCATCATCTG -3'
(R):5'- TCATAGTAACTGAGCCAGCAG -3'

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