Incidental Mutation 'R5656:Olfr497'
ID 442323
Institutional Source Beutler Lab
Gene Symbol Olfr497
Ensembl Gene ENSMUSG00000095239
Gene Name olfactory receptor 497
Synonyms GA_x6K02T2PBJ9-10752603-10753547, MOR204-9
MMRRC Submission 043302-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.084) question?
Stock # R5656 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 108420421-108424911 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 108422618 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Valine at position 16 (I16V)
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: I16V

PolyPhen 2 Score 0.027 (Sensitivity: 0.95; Specificity: 0.81)
SMART Domains Protein: ENSMUSP00000075741
Gene: ENSMUSG00000095239
AA Change: I16V

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: I16V
Predicted Effect probably benign
Transcript: ENSMUST00000213521
AA Change: I16V

PolyPhen 2 Score 0.027 (Sensitivity: 0.95; Specificity: 0.81)
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.1%
  • 20x: 94.9%
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: 60 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933405L10Rik A G 8: 105,709,512 (GRCm38) S139G probably benign Het
Adrb3 T C 8: 27,227,377 (GRCm38) D348G probably damaging Het
Atg2b A G 12: 105,621,328 (GRCm38) V1959A probably benign Het
Bicral G A 17: 46,808,369 (GRCm38) T742M probably damaging Het
Bub1b T A 2: 118,605,431 (GRCm38) I60N probably damaging Het
Ccdc162 A G 10: 41,569,934 (GRCm38) V414A probably benign Het
Cd22 T G 7: 30,869,773 (GRCm38) Y612S probably damaging Het
Cd68 T A 11: 69,664,421 (GRCm38) I320F probably damaging Het
Clca3a2 A T 3: 144,797,632 (GRCm38) N852K probably benign Het
Cpa6 T A 1: 10,329,514 (GRCm38) H363L probably benign Het
Ddx18 A T 1: 121,561,358 (GRCm38) L320Q probably damaging Het
Dnah5 A G 15: 28,421,064 (GRCm38) D3849G probably benign Het
Eci1 T A 17: 24,437,309 (GRCm38) N164K probably damaging Het
Efs T C 14: 54,917,127 (GRCm38) T552A probably damaging Het
Fbp1 C A 13: 62,875,196 (GRCm38) V96L probably damaging Het
Gtf3c1 T A 7: 125,662,654 (GRCm38) N1139I probably benign Het
Gucy1b2 T C 14: 62,422,981 (GRCm38) Y152C probably damaging Het
Gxylt1 A T 15: 93,245,661 (GRCm38) L362Q probably damaging Het
Iqcd A G 5: 120,605,126 (GRCm38) probably null Het
Klhl41 T A 2: 69,683,532 (GRCm38) I585N possibly damaging Het
Map6 A G 7: 99,336,298 (GRCm38) K470E probably damaging Het
Mast3 T C 8: 70,786,221 (GRCm38) T496A probably damaging Het
Mbd6 A T 10: 127,285,286 (GRCm38) probably benign Het
Melk A G 4: 44,312,237 (GRCm38) K183R possibly damaging Het
Mta1 T C 12: 113,123,139 (GRCm38) V152A probably damaging Het
Naa35 G A 13: 59,622,866 (GRCm38) probably benign Het
Nav3 A C 10: 109,764,633 (GRCm38) S1378A probably damaging Het
Ncapd3 T A 9: 27,051,645 (GRCm38) D415E possibly damaging Het
Nlrp4f G A 13: 65,190,871 (GRCm38) R651* probably null Het
Olfr1480 A G 19: 13,530,380 (GRCm38) T280A probably benign Het
Olfr397 T A 11: 73,964,710 (GRCm38) M34K probably damaging Het
P2rx7 A T 5: 122,673,717 (GRCm38) R364W probably damaging Het
Phactr2 T C 10: 13,388,703 (GRCm38) D2G probably benign Het
Phc3 G T 3: 30,965,866 (GRCm38) S28R probably damaging Het
Ppfia1 A T 7: 144,519,974 (GRCm38) probably null Het
Prdm10 C T 9: 31,353,417 (GRCm38) T667M probably benign Het
Pwwp2b T A 7: 139,255,971 (GRCm38) S443T possibly damaging Het
Pzp T C 6: 128,490,072 (GRCm38) T1113A probably damaging Het
Rapgef6 A G 11: 54,636,136 (GRCm38) E551G possibly damaging Het
Sec23ip A G 7: 128,776,784 (GRCm38) Y774C probably damaging Het
Setdb2 T C 14: 59,419,118 (GRCm38) D266G probably damaging Het
Shank1 T C 7: 44,352,886 (GRCm38) V1343A probably benign Het
Slf2 T A 19: 44,973,235 (GRCm38) D1064E probably benign Het
Slu7 A G 11: 43,443,418 (GRCm38) K424E probably benign Het
Smg1 A T 7: 118,154,664 (GRCm38) probably benign Het
Sptlc2 A T 12: 87,346,761 (GRCm38) L264Q probably damaging Het
Sra1 A G 18: 36,678,407 (GRCm38) S93P probably damaging Het
Sult1c1 T C 17: 53,964,652 (GRCm38) E169G probably benign Het
Sv2a A G 3: 96,185,572 (GRCm38) D196G probably damaging Het
Tbc1d22b A G 17: 29,594,780 (GRCm38) I362M probably damaging Het
Tenm3 T C 8: 48,228,762 (GRCm38) D2611G probably damaging Het
Tmem43 T C 6: 91,480,708 (GRCm38) F191L probably benign Het
Trbv13-2 T A 6: 41,121,694 (GRCm38) Y68N probably benign Het
Ttn T G 2: 76,774,654 (GRCm38) D18312A possibly damaging Het
Ublcp1 A G 11: 44,465,606 (GRCm38) V95A probably damaging Het
Usp17ld A G 7: 103,250,840 (GRCm38) V295A probably damaging Het
Vmn1r29 T A 6: 58,308,167 (GRCm38) L291M possibly damaging Het
Vsig10l C T 7: 43,464,151 (GRCm38) R176* probably null Het
Zbtb46 A G 2: 181,423,417 (GRCm38) probably null Het
Zfp644 A G 5: 106,637,982 (GRCm38) V233A probably benign Het
Other mutations in Olfr497
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01448:Olfr497 APN 7 108,423,028 (GRCm38) nonsense probably null
IGL03145:Olfr497 APN 7 108,422,599 (GRCm38) missense probably benign 0.00
R0732:Olfr497 UTSW 7 108,422,577 (GRCm38) missense probably benign 0.00
R1892:Olfr497 UTSW 7 108,422,940 (GRCm38) missense possibly damaging 0.61
R2008:Olfr497 UTSW 7 108,423,182 (GRCm38) missense probably benign 0.01
R3721:Olfr497 UTSW 7 108,423,119 (GRCm38) missense probably damaging 1.00
R4497:Olfr497 UTSW 7 108,422,915 (GRCm38) missense probably benign 0.37
R4674:Olfr497 UTSW 7 108,423,102 (GRCm38) missense possibly damaging 0.65
R4675:Olfr497 UTSW 7 108,423,102 (GRCm38) missense possibly damaging 0.65
R4695:Olfr497 UTSW 7 108,422,989 (GRCm38) missense probably benign 0.18
R5265:Olfr497 UTSW 7 108,423,402 (GRCm38) missense possibly damaging 0.94
R5758:Olfr497 UTSW 7 108,423,162 (GRCm38) missense probably benign 0.02
R6124:Olfr497 UTSW 7 108,423,518 (GRCm38) splice site probably null
R6787:Olfr497 UTSW 7 108,422,682 (GRCm38) missense possibly damaging 0.52
R7174:Olfr497 UTSW 7 108,423,160 (GRCm38) missense probably benign 0.01
R7222:Olfr497 UTSW 7 108,422,637 (GRCm38) missense probably benign 0.00
R7240:Olfr497 UTSW 7 108,422,933 (GRCm38) missense probably damaging 1.00
R8752:Olfr497 UTSW 7 108,423,273 (GRCm38) missense probably benign
R9548:Olfr497 UTSW 7 108,423,209 (GRCm38) missense possibly damaging 0.75
R9786:Olfr497 UTSW 7 108,422,717 (GRCm38) missense probably benign 0.28
Predicted Primers PCR Primer

Sequencing Primer
Posted On 2016-11-09