Incidental Mutation 'R9083:Or7g17'
ID 690404
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 068902-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.231) question?
Stock # R9083 (G1)
Quality Score 225.009
Status Validated
Chromosome 9
Chromosomal Location 18767923-18768888 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 18768550 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 201 (I201F)
Ref Sequence ENSEMBL: ENSMUSP00000148395 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000058411] [ENSMUST00000212229]
AlphaFold Q8VGX1
Predicted Effect probably benign
Transcript: ENSMUST00000058411
AA Change: I210F

PolyPhen 2 Score 0.008 (Sensitivity: 0.96; Specificity: 0.76)
SMART Domains Protein: ENSMUSP00000058101
Gene: ENSMUSG00000051414
AA Change: I210F

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: I201F

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
Meta Mutation Damage Score 0.0846 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.5%
Validation Efficiency 100% (61/61)
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: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2ml1 A T 6: 128,534,524 (GRCm39) S844R possibly damaging Het
Adig C A 2: 158,347,709 (GRCm39) probably benign Het
Aspm A G 1: 139,421,436 (GRCm39) N3106S possibly damaging Het
Bcas1 A T 2: 170,190,081 (GRCm39) probably benign Het
Bco1 A C 8: 117,844,143 (GRCm39) I286L probably benign Het
Bnc1 C T 7: 81,624,646 (GRCm39) V194I probably benign Het
Bptf G A 11: 106,959,176 (GRCm39) R1912W probably damaging Het
Cacna1a A G 8: 85,344,511 (GRCm39) I1858V probably benign Het
Chdh T C 14: 29,753,703 (GRCm39) F204S probably damaging Het
Cic A G 7: 24,985,470 (GRCm39) T1212A probably damaging Het
Cpne7 C T 8: 123,856,951 (GRCm39) P402L probably damaging Het
Cts8 A G 13: 61,397,036 (GRCm39) Y295H probably damaging Het
Cyp1a2 T C 9: 57,587,572 (GRCm39) T333A probably benign Het
Cyp2a12 T C 7: 26,735,944 (GRCm39) F451S probably damaging Het
Dmxl2 T C 9: 54,316,548 (GRCm39) I1613V probably benign Het
Eme1 A G 11: 94,540,958 (GRCm39) L260S probably damaging Het
Ermp1 A C 19: 29,623,415 (GRCm39) S192A probably benign Het
Fam186a T C 15: 99,843,079 (GRCm39) Q1055R probably benign Het
Fat1 C T 8: 45,466,127 (GRCm39) T1462M possibly damaging Het
Fat1 A G 8: 45,491,336 (GRCm39) N3822S probably benign Het
Gm973 A G 1: 59,675,317 (GRCm39) T225A Het
Gnl2 A G 4: 124,941,357 (GRCm39) Y367C probably damaging Het
Golga5 T A 12: 102,458,476 (GRCm39) S640T probably benign Het
Inafm1 A G 7: 16,007,196 (GRCm39) V7A unknown Het
Irx2 A G 13: 72,777,392 (GRCm39) D71G possibly damaging Het
Kash5 G A 7: 44,854,058 (GRCm39) R24C unknown Het
Kif13a T C 13: 46,966,263 (GRCm39) Y448C probably damaging Het
Lcor G T 19: 41,574,839 (GRCm39) R1198L probably damaging Het
Ldlrad4 A T 18: 68,197,746 (GRCm39) N10I probably benign Het
Lix1 T C 17: 17,677,392 (GRCm39) Y196H possibly damaging Het
Lrrc37 A C 11: 103,509,830 (GRCm39) S713A unknown Het
Mon1a A G 9: 107,779,835 (GRCm39) Y468C probably damaging Het
Mroh4 A T 15: 74,498,140 (GRCm39) I177N probably damaging Het
Mterf4 A T 1: 93,229,515 (GRCm39) Y236* probably null Het
Myo1f T A 17: 33,813,036 (GRCm39) I614N probably damaging Het
Nbas T A 12: 13,385,856 (GRCm39) S707T possibly damaging Het
Ncl A T 1: 86,279,183 (GRCm39) S577T possibly damaging Het
Or10al4 T A 17: 38,037,060 (GRCm39) N48K probably damaging Het
Or52d13 T C 7: 103,109,896 (GRCm39) D173G Het
Or6c2b A T 10: 128,947,892 (GRCm39) M134K probably damaging Het
Or6c69c A T 10: 129,910,941 (GRCm39) M221L probably benign Het
Or6c69c G C 10: 129,910,969 (GRCm39) S230T probably benign Het
Or8g17 A G 9: 38,930,016 (GRCm39) S274P probably damaging Het
Padi1 C A 4: 140,559,602 (GRCm39) probably null Het
Patj G A 4: 98,401,871 (GRCm39) V1004M probably benign Het
Pcdhb9 A T 18: 37,535,770 (GRCm39) D588V probably damaging Het
Pdzph1 C A 17: 59,261,395 (GRCm39) R879L possibly damaging Het
Pla2g2c G A 4: 138,463,378 (GRCm39) V91I probably benign Het
Plin4 T C 17: 56,416,345 (GRCm39) D53G possibly damaging Het
Poll T C 19: 45,546,317 (GRCm39) Q241R probably benign Het
Recql5 A T 11: 115,785,475 (GRCm39) L674M possibly damaging Het
Shroom3 G A 5: 93,098,533 (GRCm39) G1338S probably damaging Het
Slc38a8 C T 8: 120,212,780 (GRCm39) V294I probably benign Het
Slc4a1ap T C 5: 31,684,457 (GRCm39) V31A probably benign Het
Tln2 G A 9: 67,269,927 (GRCm39) P489S probably damaging Het
Trappc9 G A 15: 72,608,626 (GRCm39) R928* probably null Het
Uba7 C A 9: 107,855,166 (GRCm39) T343N probably benign Het
Vasn C T 16: 4,467,871 (GRCm39) T606I probably benign Het
Xrn2 T A 2: 146,880,199 (GRCm39) D507E probably damaging Het
Zfp592 T A 7: 80,674,644 (GRCm39) M536K possibly damaging Het
Zfp932 A T 5: 110,157,100 (GRCm39) H266L probably damaging 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
R4090:Or7g17 UTSW 9 18,768,398 (GRCm39) missense probably benign 0.00
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
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'- GACCGCTATGTTGCTATTTGCC -3'
(R):5'- CACAGCACTCTTCCTGGATG -3'

Sequencing Primer
(F):5'- GCCATCCACTTAGGTATAGGATC -3'
(R):5'- TTGTTGAGCTGATATAGACCCC -3'
Posted On 2021-12-30