Incidental Mutation 'R0089:Olfr677'
ID20061
Institutional Source Beutler Lab
Gene Symbol Olfr677
Ensembl Gene ENSMUSG00000073914
Gene Nameolfactory receptor 677
SynonymsGA_x6K02T2PBJ9-7685262-7686200, MOR32-11
MMRRC Submission 038376-MU
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.359) question?
Stock #R0089 (G1)
Quality Score225
Status Validated (trace)
Chromosome7
Chromosomal Location105051372-105059006 bp(+) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) T to A at 105057090 bp
ZygosityHeterozygous
Amino Acid Change Tyrosine to Stop codon at position 281 (Y281*)
Ref Sequence ENSEMBL: ENSMUSP00000149888 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000098161] [ENSMUST00000213204]
Predicted Effect probably null
Transcript: ENSMUST00000098161
AA Change: Y281*
SMART Domains Protein: ENSMUSP00000095764
Gene: ENSMUSG00000073914
AA Change: Y281*

DomainStartEndE-ValueType
Pfam:7tm_4 33 311 7.6e-120 PFAM
Pfam:7TM_GPCR_Srsx 37 308 4.8e-6 PFAM
Pfam:7tm_1 43 293 1.3e-16 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000209491
Predicted Effect probably null
Transcript: ENSMUST00000213204
AA Change: Y281*
Meta Mutation Damage Score 0.634 question?
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 97.9%
  • 10x: 95.6%
  • 20x: 90.5%
Validation Efficiency 98% (82/84)
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: 78 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 T A 11: 9,292,886 V1583E possibly damaging Het
Ablim1 G T 19: 57,043,031 S654Y probably damaging Het
Acbd4 T C 11: 103,103,993 F59S probably damaging Het
Acot1 T C 12: 84,016,934 I272T probably damaging Het
Ankhd1 A G 18: 36,640,356 D1402G probably damaging Het
Birc6 T A 17: 74,638,376 F2800I possibly damaging Het
Brd1 T C 15: 88,701,198 E811G probably benign Het
Ccdc106 A G 7: 5,056,221 probably null Het
Ccdc81 G T 7: 89,893,116 A184E possibly damaging Het
Cenpt T C 8: 105,846,368 T364A probably benign Het
Crybg2 T C 4: 134,081,194 S1060P probably damaging Het
Dnttip2 A G 3: 122,275,462 T109A possibly damaging Het
Dpy19l2 A G 9: 24,695,793 L124P probably benign Het
Fat3 T C 9: 15,938,205 D3967G probably benign Het
Fbxo21 T A 5: 118,008,143 F610L probably benign Het
Fmo9 T C 1: 166,667,309 D341G probably benign Het
Frem3 A T 8: 80,615,878 H1600L possibly damaging Het
Fry A T 5: 150,340,427 K133N possibly damaging Het
Gm10647 A G 9: 66,798,330 probably benign Het
Gm13124 T A 4: 144,555,733 H163L probably benign Het
Gm16432 C T 1: 178,046,989 P141S unknown Het
Gm21319 A T 12: 87,773,513 I92N probably damaging Het
Gmps T C 3: 63,998,698 F472S probably benign Het
Grb10 T C 11: 11,934,192 probably benign Het
Grm6 G A 11: 50,859,965 G652S probably damaging Het
Heca G T 10: 17,908,100 D468E probably damaging Het
Heg1 C T 16: 33,763,615 S1033L probably damaging Het
Hepacam2 A G 6: 3,487,094 S12P probably damaging Het
Impdh1 G T 6: 29,206,326 H195N probably benign Het
Ipo7 T C 7: 110,050,765 probably benign Het
Itpr2 C T 6: 146,350,022 probably null Het
Kcnh6 G A 11: 106,009,022 C39Y probably benign Het
Kif26a T C 12: 112,177,403 S1364P probably damaging Het
Lins1 T A 7: 66,712,048 probably benign Het
Lrpap1 C T 5: 35,094,888 V328M possibly damaging Het
Lyn T G 4: 3,748,768 L249V probably benign Het
Mpp7 A G 18: 7,439,555 probably benign Het
Mtmr9 A G 14: 63,528,247 F400L possibly damaging Het
Mto1 G A 9: 78,473,872 S666N probably benign Het
Nanos3 C T 8: 84,176,134 R133Q probably damaging Het
Nsg1 T C 5: 38,155,630 E75G probably benign Het
Nsun4 A G 4: 116,035,773 M283T probably benign Het
Obscn A G 11: 59,000,062 S7215P unknown Het
Olfr1042 A C 2: 86,159,574 S265R possibly damaging Het
Olfr1160 T C 2: 88,005,987 I264V probably damaging Het
Olfr1383 G A 11: 49,524,206 S161N possibly damaging Het
Olfr340 G A 2: 36,453,095 R170K probably benign Het
Olfr53 T C 7: 140,652,311 S111P probably damaging Het
Olfr736 T C 14: 50,392,864 I36T probably benign Het
Per1 T C 11: 69,104,043 F563S probably benign Het
Pik3c3 T A 18: 30,303,078 probably benign Het
Pitrm1 A T 13: 6,555,639 K207N probably damaging Het
Prdm10 C T 9: 31,316,230 R44C probably damaging Het
Rab40c A T 17: 25,885,148 I90N probably damaging Het
Rbl1 A G 2: 157,199,414 probably null Het
Rnf17 G A 14: 56,514,106 G1467E probably damaging Het
Rpgrip1 A G 14: 52,149,384 probably benign Het
Sall1 A T 8: 89,030,268 N1069K probably benign Het
Scap T C 9: 110,372,222 I93T possibly damaging Het
Sez6 T C 11: 77,974,344 probably benign Het
Slc22a30 A T 19: 8,370,197 S280T probably benign Het
Slc26a5 A C 5: 21,811,344 probably null Het
St18 T C 1: 6,848,948 V901A probably benign Het
Syne2 T C 12: 75,963,876 L2519P probably damaging Het
Syne4 G A 7: 30,318,919 G362E probably damaging Het
Tmem51 T C 4: 142,031,925 T171A probably benign Het
Tns4 A T 11: 99,075,198 I453N probably damaging Het
Trank1 A T 9: 111,392,910 H2905L probably benign Het
Trim13 C T 14: 61,604,717 T61I possibly damaging Het
Trim75 T C 8: 64,982,928 Q290R possibly damaging Het
Ttn C A 2: 76,729,200 R29619L probably damaging Het
Ugt2b38 T A 5: 87,420,558 M293L probably benign Het
Vmn1r22 T A 6: 57,900,528 N155Y probably benign Het
Vmn2r18 T C 5: 151,584,804 Y285C probably benign Het
Vmn2r84 C T 10: 130,386,719 probably benign Het
Vwde A C 6: 13,220,005 L49R probably damaging Het
Yipf2 T A 9: 21,591,966 E68D possibly damaging Het
Zfand5 C A 19: 21,279,758 probably benign Het
Other mutations in Olfr677
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02111:Olfr677 APN 7 105056945 missense probably benign 0.10
IGL02351:Olfr677 APN 7 105056975 missense probably damaging 0.98
IGL02358:Olfr677 APN 7 105056975 missense probably damaging 0.98
IGL02696:Olfr677 APN 7 105056362 missense probably benign 0.39
R0963:Olfr677 UTSW 7 105056972 missense probably damaging 0.98
R1157:Olfr677 UTSW 7 105056884 missense probably benign 0.01
R1719:Olfr677 UTSW 7 105056794 missense probably damaging 0.97
R1998:Olfr677 UTSW 7 105056905 missense probably benign 0.05
R2039:Olfr677 UTSW 7 105056390 missense possibly damaging 0.75
R2180:Olfr677 UTSW 7 105056885 missense probably benign 0.18
R2568:Olfr677 UTSW 7 105056671 missense probably benign 0.00
R4700:Olfr677 UTSW 7 105056276 missense possibly damaging 0.81
R4701:Olfr677 UTSW 7 105056879 missense probably damaging 1.00
R4803:Olfr677 UTSW 7 105056656 missense probably benign 0.39
R4888:Olfr677 UTSW 7 105056482 missense possibly damaging 0.95
R5121:Olfr677 UTSW 7 105056482 missense possibly damaging 0.95
R5190:Olfr677 UTSW 7 105056453 missense probably damaging 0.96
R5593:Olfr677 UTSW 7 105056504 missense probably damaging 1.00
R6831:Olfr677 UTSW 7 105056879 missense possibly damaging 0.95
Predicted Primers PCR Primer
(F):5'- GATGCCCGATTGAAGGCGCTAAAC -3'
(R):5'- TTTGTCCAGACATGTGGAGGGAGC -3'

Sequencing Primer
(F):5'- TTGAAGGCGCTAAACACTTGTG -3'
(R):5'- GCATTTGGATCAAAGTGCTAGAC -3'
Posted On2013-04-11