Incidental Mutation 'R0415:Olfr78'
ID 40242
Institutional Source Beutler Lab
Gene Symbol Olfr78
Ensembl Gene ENSMUSG00000043366
Gene Name olfactory receptor 78
Synonyms MOL2.3, GA_x6K02T2PBJ9-5459657-5458695, 4633402A21Rik, RA1c, MOR18-2, PSGR
MMRRC Submission 038617-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.060) question?
Stock # R0415 (G1)
Quality Score 215
Status Validated
Chromosome 7
Chromosomal Location 102738511-102759471 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) C to T at 102742087 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Methionine to Isoleucine at position 305 (M305I)
Ref Sequence ENSEMBL: ENSMUSP00000149274 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000060187] [ENSMUST00000168007] [ENSMUST00000217123]
AlphaFold Q8VBV9
Predicted Effect probably benign
Transcript: ENSMUST00000060187
AA Change: M305I

PolyPhen 2 Score 0.021 (Sensitivity: 0.95; Specificity: 0.80)
SMART Domains Protein: ENSMUSP00000058085
Gene: ENSMUSG00000043366
AA Change: M305I

DomainStartEndE-ValueType
Pfam:7tm_4 30 309 1.9e-111 PFAM
Pfam:7TM_GPCR_Srsx 34 252 1.4e-8 PFAM
Pfam:7tm_1 40 291 2.3e-17 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000168007
AA Change: M305I

PolyPhen 2 Score 0.021 (Sensitivity: 0.95; Specificity: 0.80)
SMART Domains Protein: ENSMUSP00000133255
Gene: ENSMUSG00000043366
AA Change: M305I

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srsx 34 252 1.4e-8 PFAM
Pfam:7tm_1 40 291 1.4e-25 PFAM
Pfam:7tm_4 140 284 2.8e-27 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000209365
Predicted Effect probably benign
Transcript: ENSMUST00000217123
AA Change: M305I

PolyPhen 2 Score 0.021 (Sensitivity: 0.95; Specificity: 0.80)
Meta Mutation Damage Score 0.1056 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.7%
  • 20x: 93.6%
Validation Efficiency 97% (99/102)
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]
PHENOTYPE: Targeted inactivation of this gene leads to alterations in olfactory sensory neuron development. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 98 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933427G23Rik A T 5: 23,831,050 (GRCm38) noncoding transcript Het
Acox2 A G 14: 8,243,835 (GRCm38) probably benign Het
Adgb T C 10: 10,431,067 (GRCm38) probably null Het
Adgra3 C A 5: 49,961,757 (GRCm38) probably benign Het
Adgre4 G A 17: 55,852,288 (GRCm38) V658I probably benign Het
Ahnak A G 19: 9,012,871 (GRCm38) probably benign Het
Anapc2 A G 2: 25,278,325 (GRCm38) T159A probably damaging Het
Arfgef3 A G 10: 18,613,127 (GRCm38) probably benign Het
Atf7ip C T 6: 136,560,012 (GRCm38) S81L possibly damaging Het
Cacna1i A G 15: 80,368,830 (GRCm38) probably benign Het
Camk1 A T 6: 113,341,891 (GRCm38) Y20* probably null Het
Ccdc40 T C 11: 119,232,118 (GRCm38) Y249H possibly damaging Het
Cd109 T A 9: 78,712,615 (GRCm38) S1380T probably benign Het
Cfap57 A T 4: 118,569,431 (GRCm38) L1107Q possibly damaging Het
Col6a4 C T 9: 106,075,080 (GRCm38) V540I probably damaging Het
Cst9 T A 2: 148,838,442 (GRCm38) probably benign Het
Cul5 C T 9: 53,667,070 (GRCm38) V73I probably benign Het
Cxcl16 T A 11: 70,458,748 (GRCm38) K84* probably null Het
Cyp2c29 T C 19: 39,329,095 (GRCm38) probably benign Het
D6Ertd527e C G 6: 87,111,524 (GRCm38) T223S unknown Het
Dip2c C T 13: 9,568,289 (GRCm38) probably benign Het
Dis3 A T 14: 99,087,456 (GRCm38) I513N probably damaging Het
Dnajc16 A T 4: 141,789,048 (GRCm38) L3* probably null Het
Dopey1 T A 9: 86,506,502 (GRCm38) L480M probably damaging Het
Eml6 A G 11: 29,749,392 (GRCm38) V1787A possibly damaging Het
Etnk1 A G 6: 143,180,774 (GRCm38) N115S probably damaging Het
Fryl T C 5: 73,098,414 (GRCm38) Y758C probably damaging Het
Gbp4 G A 5: 105,121,106 (GRCm38) R394C possibly damaging Het
Ggnbp2 A C 11: 84,833,225 (GRCm38) probably benign Het
Gm7137 A G 10: 77,788,173 (GRCm38) probably benign Het
Gstm2 T A 3: 107,984,006 (GRCm38) Q132L probably benign Het
Habp2 T C 19: 56,317,717 (GRCm38) probably benign Het
Hectd2 T C 19: 36,584,884 (GRCm38) probably benign Het
Htr6 A G 4: 139,062,081 (GRCm38) I291T possibly damaging Het
Ighg2c T C 12: 113,287,910 (GRCm38) D199G unknown Het
Itih2 A G 2: 10,105,615 (GRCm38) probably benign Het
Kcnab2 A G 4: 152,395,136 (GRCm38) F248S probably benign Het
Kcnc4 T C 3: 107,445,433 (GRCm38) K610E probably damaging Het
Kcnk16 T A 14: 20,262,975 (GRCm38) probably null Het
Kndc1 C T 7: 139,930,124 (GRCm38) T1293I probably damaging Het
Lcp1 A T 14: 75,227,006 (GRCm38) I556F possibly damaging Het
Lrrc8d T C 5: 105,811,865 (GRCm38) L47P probably damaging Het
Lyst T C 13: 13,711,610 (GRCm38) probably benign Het
Macrod2 G A 2: 142,210,145 (GRCm38) probably null Het
Micalcl C T 7: 112,381,028 (GRCm38) R70C probably damaging Het
Mllt3 ACTGCTGCTGCTGCTGCTGCT ACTGCTGCTGCTGCTGCT 4: 87,841,339 (GRCm38) probably benign Het
Msh3 A G 13: 92,346,786 (GRCm38) V283A possibly damaging Het
Nup205 T C 6: 35,214,634 (GRCm38) probably benign Het
Nxpe2 T C 9: 48,326,614 (GRCm38) T114A probably damaging Het
Olfr1023 A T 2: 85,887,438 (GRCm38) I213F possibly damaging Het
Olfr1034 A T 2: 86,047,055 (GRCm38) H191L probably benign Het
Olfr229 A G 9: 39,909,983 (GRCm38) Y60C probably damaging Het
Olfr893 A T 9: 38,209,973 (GRCm38) M305L probably benign Het
Pard3 G A 8: 127,610,566 (GRCm38) G1221D probably damaging Het
Pax5 G A 4: 44,691,886 (GRCm38) A120V probably damaging Het
Pcsk6 C T 7: 66,033,874 (GRCm38) R746C probably damaging Het
Pif1 G A 9: 65,588,051 (GRCm38) C81Y probably benign Het
Plcb1 A G 2: 135,337,499 (GRCm38) Y609C probably damaging Het
Plcd4 C A 1: 74,552,097 (GRCm38) S217Y probably damaging Het
Plxna1 G A 6: 89,357,336 (GRCm38) H104Y probably benign Het
Polr2k A G 15: 36,175,456 (GRCm38) Y45C probably damaging Het
Pqlc3 C A 12: 16,997,710 (GRCm38) probably benign Het
Prex1 A G 2: 166,586,699 (GRCm38) probably benign Het
Pth2r A G 1: 65,388,439 (GRCm38) M424V probably benign Het
Pygm A G 19: 6,391,366 (GRCm38) R464G probably benign Het
Rad51c A G 11: 87,397,655 (GRCm38) L234P probably damaging Het
Rnf145 A G 11: 44,525,138 (GRCm38) Y60C probably damaging Het
Rnf167 T C 11: 70,649,699 (GRCm38) I135T probably damaging Het
Rnf213 A T 11: 119,414,469 (GRCm38) I509F probably damaging Het
Ryr2 T C 13: 11,869,156 (GRCm38) S213G probably damaging Het
Selenbp1 T C 3: 94,936,913 (GRCm38) V27A possibly damaging Het
Selenof T G 3: 144,577,692 (GRCm38) L14R probably damaging Het
Sfswap A T 5: 129,504,126 (GRCm38) D121V probably damaging Het
Slc25a34 C A 4: 141,620,469 (GRCm38) M300I possibly damaging Het
Slc34a3 T G 2: 25,229,110 (GRCm38) T583P probably benign Het
Smg1 C A 7: 118,182,468 (GRCm38) A1199S probably benign Het
Spint1 A G 2: 119,245,615 (GRCm38) T231A probably damaging Het
Sptbn1 A C 11: 30,149,576 (GRCm38) N229K probably damaging Het
Sult2b1 A G 7: 45,730,092 (GRCm38) probably benign Het
Tas2r123 A T 6: 132,847,838 (GRCm38) M233L probably damaging Het
Tbcel C A 9: 42,444,500 (GRCm38) C139F probably benign Het
Thbs2 A C 17: 14,679,973 (GRCm38) S573A probably benign Het
Tmem132c A G 5: 127,563,705 (GRCm38) E980G probably damaging Het
Tmem247 G T 17: 86,922,322 (GRCm38) C197F probably damaging Het
Tmem251 T A 12: 102,744,876 (GRCm38) Y119* probably null Het
Tmem43 C A 6: 91,482,318 (GRCm38) P257Q probably benign Het
Tmprss13 A G 9: 45,337,132 (GRCm38) probably null Het
Trove2 G T 1: 143,760,075 (GRCm38) N444K probably benign Het
Ubr5 T C 15: 37,972,980 (GRCm38) T2626A probably damaging Het
Vmn1r196 T A 13: 22,293,836 (GRCm38) V215D probably damaging Het
Vmn1r22 G T 6: 57,900,332 (GRCm38) T220K probably benign Het
Vmn2r116 G A 17: 23,387,279 (GRCm38) M388I possibly damaging Het
Vmn2r74 A C 7: 85,961,410 (GRCm38) C25G probably damaging Het
Xndc1 T C 7: 102,080,616 (GRCm38) probably benign Het
Zfp282 T A 6: 47,905,053 (GRCm38) I558N possibly damaging Het
Zfp282 A G 6: 47,897,881 (GRCm38) D340G probably damaging Het
Zfp316 T A 5: 143,264,491 (GRCm38) T56S unknown Het
Zfp345 A G 2: 150,474,559 (GRCm38) probably benign Het
Other mutations in Olfr78
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00940:Olfr78 APN 7 102,742,262 (GRCm38) missense probably damaging 1.00
IGL02071:Olfr78 APN 7 102,742,148 (GRCm38) missense probably damaging 1.00
IGL03166:Olfr78 APN 7 102,742,047 (GRCm38) missense probably benign 0.00
R0781:Olfr78 UTSW 7 102,743,007 (GRCm38) utr 5 prime probably benign
R1676:Olfr78 UTSW 7 102,742,398 (GRCm38) missense probably damaging 1.00
R1858:Olfr78 UTSW 7 102,742,364 (GRCm38) missense probably damaging 1.00
R2391:Olfr78 UTSW 7 102,742,374 (GRCm38) missense possibly damaging 0.63
R4542:Olfr78 UTSW 7 102,742,643 (GRCm38) missense probably damaging 1.00
R4671:Olfr78 UTSW 7 102,742,601 (GRCm38) missense probably damaging 0.98
R5400:Olfr78 UTSW 7 102,742,430 (GRCm38) missense probably benign 0.00
R7015:Olfr78 UTSW 7 102,742,444 (GRCm38) missense probably damaging 1.00
R7133:Olfr78 UTSW 7 102,742,317 (GRCm38) missense probably damaging 1.00
R7247:Olfr78 UTSW 7 102,742,344 (GRCm38) missense probably damaging 0.99
R8259:Olfr78 UTSW 7 102,742,827 (GRCm38) missense probably damaging 1.00
R8772:Olfr78 UTSW 7 102,743,003 (GRCm38) start gained probably benign
R9095:Olfr78 UTSW 7 102,742,266 (GRCm38) missense possibly damaging 0.54
Predicted Primers PCR Primer
(F):5'- TGAGCGAGGAAACATACTGTCAGC -3'
(R):5'- AGCGAGCTAAGGCATTTGGGAC -3'

Sequencing Primer
(F):5'- GGAAACATACTGTCAGCTTCATGC -3'
(R):5'- CTAAGGCATTTGGGACTTGTG -3'
Posted On 2013-05-23