Incidental Mutation 'R4090:Or7g17'
ID 317567
Institutional Source Beutler Lab
Gene Symbol Or7g17
Ensembl Gene ENSMUSG00000051414
Gene Name olfactory receptor family 7 subfamily G member 17
Synonyms Olfr829, GA_x6K02T2PVTD-12599710-12600648, MOR147-1
MMRRC Submission 040983-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.231) question?
Stock # R4090 (G1)
Quality Score 225
Status Validated
Chromosome 9
Chromosomal Location 18767923-18768888 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 18768398 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Threonine at position 159 (I159T)
Ref Sequence ENSEMBL: ENSMUSP00000058101 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000058411] [ENSMUST00000212229]
AlphaFold Q8VGX1
Predicted Effect probably benign
Transcript: ENSMUST00000058411
AA Change: I159T

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
SMART Domains Protein: ENSMUSP00000058101
Gene: ENSMUSG00000051414
AA Change: I159T

DomainStartEndE-ValueType
Pfam:7tm_4 40 317 2e-52 PFAM
Pfam:7TM_GPCR_Srsx 44 174 1e-10 PFAM
Pfam:7tm_1 50 299 1.6e-21 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000212229
AA Change: I150T

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.7%
Validation Efficiency 96% (53/55)
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: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acss3 T G 10: 106,889,313 (GRCm39) Y169S probably damaging Het
Apc2 A G 10: 80,141,378 (GRCm39) K268E probably damaging Het
Arhgef2 G C 3: 88,551,185 (GRCm39) R765P probably benign Het
Bptf T C 11: 106,972,349 (GRCm39) K840E probably damaging Het
Carf A G 1: 60,175,506 (GRCm39) R245G possibly damaging Het
Cd36 A G 5: 17,990,718 (GRCm39) probably null Het
Cep250 G A 2: 155,834,552 (GRCm39) R2159K probably damaging Het
Cldn34c4 A T X: 126,629,011 (GRCm39) V153E probably damaging Het
Col4a4 T A 1: 82,501,643 (GRCm39) Y370F unknown Het
Cplane1 T A 15: 8,241,842 (GRCm39) probably null Het
Ddx4 A G 13: 112,750,295 (GRCm39) V386A probably benign Het
Exoc6 A G 19: 37,560,360 (GRCm39) T126A probably benign Het
Fam83f A T 15: 80,576,393 (GRCm39) N348I possibly damaging Het
Gja8 A G 3: 96,826,468 (GRCm39) V398A probably benign Het
Gkn3 C T 6: 87,360,507 (GRCm39) A163T probably damaging Het
Gm12789 A T 4: 101,845,526 (GRCm39) T72S possibly damaging Het
Gm1988 A G 7: 38,820,292 (GRCm39) noncoding transcript Het
Gm21370 A G 13: 120,488,489 (GRCm39) V20A probably benign Het
Hjurp G C 1: 88,204,937 (GRCm39) probably benign Het
Hsd17b13 T A 5: 104,113,720 (GRCm39) S245C probably benign Het
Htr1f T C 16: 64,746,324 (GRCm39) K323E probably benign Het
Igkc T C 6: 70,703,442 (GRCm39) probably benign Het
Ksr1 T C 11: 78,918,303 (GRCm39) E535G probably damaging Het
Mlxipl A T 5: 135,161,381 (GRCm39) E433D probably benign Het
Npc1 T C 18: 12,331,219 (GRCm39) probably null Het
Or10ak7 C T 4: 118,791,230 (GRCm39) E272K probably benign Het
Or1e29 A G 11: 73,667,667 (GRCm39) L162P probably damaging Het
Or6y1 A G 1: 174,276,500 (GRCm39) T104A probably benign Het
Pcdha3 A G 18: 37,081,504 (GRCm39) R749G probably benign Het
Ppme1 A T 7: 99,997,044 (GRCm39) N122K possibly damaging Het
Rasal1 G A 5: 120,813,674 (GRCm39) V657M possibly damaging Het
Rbm47 A G 5: 66,180,080 (GRCm39) M409T probably benign Het
Rragd C T 4: 33,007,155 (GRCm39) T161M probably damaging Het
Slurp1 T C 15: 74,598,724 (GRCm39) H89R possibly damaging Het
Snap23 A G 2: 120,416,061 (GRCm39) I42V probably benign Het
Sypl2 A G 3: 108,124,992 (GRCm39) I123T possibly damaging Het
Taar8a T A 10: 23,953,062 (GRCm39) V222E probably damaging Het
Tmem171 A T 13: 98,829,096 (GRCm39) V18D probably damaging Het
Topors T C 4: 40,260,794 (GRCm39) D830G unknown Het
Traf3ip3 A G 1: 192,863,628 (GRCm39) V414A probably damaging Het
Tubg1 T A 11: 101,015,364 (GRCm39) M270K possibly damaging Het
Vmn1r188 T C 13: 22,272,772 (GRCm39) V242A probably benign Het
Vmn1r19 T A 6: 57,381,720 (GRCm39) I91N probably damaging Het
Vmn2r12 T A 5: 109,239,412 (GRCm39) M384L probably benign Het
Wdr26 T C 1: 181,030,679 (GRCm39) E205G probably damaging Het
Zfp281 T A 1: 136,553,859 (GRCm39) I279N probably damaging Het
Zfp398 T A 6: 47,843,159 (GRCm39) C272S probably damaging Het
Zfp975 A G 7: 42,312,298 (GRCm39) V105A probably benign Het
Other mutations in Or7g17
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01142:Or7g17 APN 9 18,768,830 (GRCm39) missense probably damaging 0.97
IGL01696:Or7g17 APN 9 18,768,352 (GRCm39) missense probably benign 0.19
IGL02285:Or7g17 APN 9 18,768,286 (GRCm39) missense possibly damaging 0.87
R0133:Or7g17 UTSW 9 18,767,925 (GRCm39) start codon destroyed probably null
R0173:Or7g17 UTSW 9 18,768,325 (GRCm39) missense probably damaging 0.98
R0270:Or7g17 UTSW 9 18,768,127 (GRCm39) missense probably damaging 1.00
R0449:Or7g17 UTSW 9 18,767,945 (GRCm39) missense probably benign 0.00
R1111:Or7g17 UTSW 9 18,768,888 (GRCm39) makesense probably null
R1462:Or7g17 UTSW 9 18,768,407 (GRCm39) missense probably benign 0.30
R1462:Or7g17 UTSW 9 18,768,407 (GRCm39) missense probably benign 0.30
R1845:Or7g17 UTSW 9 18,768,782 (GRCm39) missense possibly damaging 0.95
R4096:Or7g17 UTSW 9 18,767,933 (GRCm39) missense probably benign
R4097:Or7g17 UTSW 9 18,767,933 (GRCm39) missense probably benign
R4755:Or7g17 UTSW 9 18,768,476 (GRCm39) missense probably benign 0.03
R4867:Or7g17 UTSW 9 18,768,862 (GRCm39) missense probably benign 0.00
R5084:Or7g17 UTSW 9 18,768,632 (GRCm39) missense probably benign 0.43
R7216:Or7g17 UTSW 9 18,768,632 (GRCm39) missense probably benign 0.43
R7252:Or7g17 UTSW 9 18,768,548 (GRCm39) missense probably damaging 1.00
R7300:Or7g17 UTSW 9 18,768,530 (GRCm39) missense not run
R7412:Or7g17 UTSW 9 18,768,085 (GRCm39) missense possibly damaging 0.51
R8079:Or7g17 UTSW 9 18,768,725 (GRCm39) missense possibly damaging 0.54
R9083:Or7g17 UTSW 9 18,768,550 (GRCm39) missense probably benign 0.00
R9648:Or7g17 UTSW 9 18,768,748 (GRCm39) missense possibly damaging 0.84
X0024:Or7g17 UTSW 9 18,768,320 (GRCm39) missense probably damaging 1.00
X0057:Or7g17 UTSW 9 18,767,933 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- TGGAGGATGTCTGACTCAGG -3'
(R):5'- TCTCAAGACAGTGGTTGCAATTTG -3'

Sequencing Primer
(F):5'- AGGATGTCTGACTCAGGTCTGC -3'
(R):5'- GACAGTGGTTGCAATTTGACAATATG -3'
Posted On 2015-05-15