Incidental Mutation 'R7789:Or7g29'
ID 599747
Institutional Source Beutler Lab
Gene Symbol Or7g29
Ensembl Gene ENSMUSG00000059821
Gene Name olfactory receptor family 7 subfamily G member 29
Synonyms Olfr847, GA_x6K02T2PVTD-13113073-13112135, MOR149-2
MMRRC Submission 045845-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.132) question?
Stock # R7789 (G1)
Quality Score 225.009
Status Validated
Chromosome 9
Chromosomal Location 19286237-19287175 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 19286361 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Lysine at position 272 (T272K)
Ref Sequence ENSEMBL: ENSMUSP00000151112 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000079620] [ENSMUST00000216839]
AlphaFold Q8VFF4
Predicted Effect probably benign
Transcript: ENSMUST00000079620
AA Change: T272K

PolyPhen 2 Score 0.329 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000078568
Gene: ENSMUSG00000059821
AA Change: T272K

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 1.9e-56 PFAM
Pfam:7tm_1 41 290 2.1e-22 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000216839
AA Change: T272K

PolyPhen 2 Score 0.329 (Sensitivity: 0.90; Specificity: 0.89)
Meta Mutation Damage Score 0.0846 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.5%
Validation Efficiency 99% (77/78)
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: 76 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930562C15Rik G A 16: 4,682,175 (GRCm39) E163K probably benign Het
Adam34 T A 8: 44,105,488 (GRCm39) R52S probably benign Het
Adcy8 A T 15: 64,743,623 (GRCm39) C328* probably null Het
Ankrd26 G T 6: 118,504,760 (GRCm39) S716R possibly damaging Het
Ankrd26 G T 6: 118,504,759 (GRCm39) H717N probably damaging Het
Ankrd40 C A 11: 94,225,535 (GRCm39) P189T probably damaging Het
Anln A G 9: 22,263,333 (GRCm39) S113P Het
Arid5b C T 10: 67,934,417 (GRCm39) G495E probably benign Het
Asxl1 C T 2: 153,241,943 (GRCm39) T832I probably benign Het
Bicd2 C T 13: 49,533,135 (GRCm39) R574C probably damaging Het
Boll T C 1: 55,399,826 (GRCm39) probably null Het
Casr A G 16: 36,315,653 (GRCm39) F806L probably damaging Het
Casz1 C A 4: 149,013,863 (GRCm39) N142K probably benign Het
Cbl C T 9: 44,074,764 (GRCm39) D433N probably damaging Het
Ceacam14 T A 7: 17,548,096 (GRCm39) V62D probably damaging Het
Chst10 T C 1: 38,923,532 (GRCm39) N18S probably benign Het
Cyp2j6 C T 4: 96,433,953 (GRCm39) R119H probably benign Het
Cyp4a14 C G 4: 115,352,107 (GRCm39) V102L probably benign Het
Dnajb3 A T 1: 88,133,399 (GRCm39) M1K probably null Het
Dnajc6 A T 4: 101,475,729 (GRCm39) K534M possibly damaging Het
Dnase2a T C 8: 85,635,505 (GRCm39) probably null Het
Dock10 A G 1: 80,536,930 (GRCm39) I985T possibly damaging Het
Emsy G T 7: 98,270,696 (GRCm39) P436Q probably damaging Het
Enpp1 A T 10: 24,529,981 (GRCm39) probably null Het
Erc1 T A 6: 119,750,670 (GRCm39) R353* probably null Het
Fbn2 T A 18: 58,172,385 (GRCm39) D2140V probably benign Het
Fgfr1 T A 8: 26,052,329 (GRCm39) Y218* probably null Het
Fhod1 C T 8: 106,056,740 (GRCm39) R1045H probably damaging Het
Focad G T 4: 88,147,643 (GRCm39) L427F unknown Het
Gbf1 T A 19: 46,242,441 (GRCm39) L144M probably damaging Het
Glmn T G 5: 107,696,941 (GRCm39) N592T probably benign Het
Golgb1 C G 16: 36,695,761 (GRCm39) P87A unknown Het
H2bw2 G A X: 135,828,471 (GRCm39) R120K unknown Het
Insyn2b T A 11: 34,352,537 (GRCm39) M193K probably benign Het
Itga9 T G 9: 118,487,564 (GRCm39) F216V possibly damaging Het
Klhl18 T C 9: 110,268,076 (GRCm39) D149G unknown Het
Lcat C T 8: 106,668,857 (GRCm39) V114M probably benign Het
Lrrc8c C A 5: 105,755,066 (GRCm39) N280K probably damaging Het
Mettl8 T C 2: 70,796,806 (GRCm39) Y283C probably damaging Het
Mgat4a A T 1: 37,529,360 (GRCm39) I173K probably damaging Het
Mmp1a T C 9: 7,475,266 (GRCm39) V345A possibly damaging Het
Mok T A 12: 110,778,261 (GRCm39) H215L probably damaging Het
Mphosph9 C G 5: 124,453,650 (GRCm39) E221Q probably damaging Het
Muc4 C G 16: 32,575,221 (GRCm39) Q1269E probably benign Het
Mug1 C A 6: 121,838,179 (GRCm39) H470N possibly damaging Het
Myom1 A G 17: 71,424,431 (GRCm39) T1525A probably benign Het
Nap1l1 C T 10: 111,326,317 (GRCm39) S143L probably benign Het
Or1af1 C T 2: 37,109,672 (GRCm39) T57I probably benign Het
Or2j6 A T 7: 139,980,610 (GRCm39) Y116* probably null Het
Or52d1 T A 7: 103,756,195 (GRCm39) S236R probably damaging Het
Plbd2 T C 5: 120,623,819 (GRCm39) S568G probably damaging Het
Plxna4 T A 6: 32,183,168 (GRCm39) probably null Het
Plxnc1 T A 10: 94,630,339 (GRCm39) E1520V probably damaging Het
Ppil3 G A 1: 58,473,538 (GRCm39) T104I possibly damaging Het
Ptprm A T 17: 67,402,534 (GRCm39) V118E probably damaging Het
Rimbp2 T C 5: 128,851,399 (GRCm39) D849G probably damaging Het
Rnf213 T C 11: 119,361,045 (GRCm39) probably null Het
Sema3f T A 9: 107,582,631 (GRCm39) K37N probably benign Het
Sh3glb1 G T 3: 144,397,892 (GRCm39) probably null Het
Sh3rf3 A G 10: 58,922,637 (GRCm39) D571G probably benign Het
Sipa1l3 T C 7: 29,077,150 (GRCm39) Y874C probably damaging Het
Smchd1 G A 17: 71,782,296 (GRCm39) probably benign Het
Snrnp70 A T 7: 45,026,045 (GRCm39) Y441* probably null Het
Ssrp1 C T 2: 84,871,525 (GRCm39) R316W probably damaging Het
Syt10 A T 15: 89,711,101 (GRCm39) V144E probably damaging Het
Tdrd12 A G 7: 35,188,117 (GRCm39) L562P Het
Trim68 T C 7: 102,333,676 (GRCm39) D2G possibly damaging Het
Trub2 T A 2: 29,667,920 (GRCm39) H240L probably damaging Het
Tssc4 A G 7: 142,623,515 (GRCm39) probably null Het
Usp7 T A 16: 8,516,675 (GRCm39) Q539L probably benign Het
Vmn2r17 T A 5: 109,600,831 (GRCm39) C710S possibly damaging Het
Vmn2r99 G T 17: 19,614,079 (GRCm39) V600F possibly damaging Het
Vps13d C T 4: 144,826,635 (GRCm39) V2879M Het
Vrtn T A 12: 84,697,080 (GRCm39) M610K probably benign Het
Xpo4 T C 14: 57,850,806 (GRCm39) E366G probably benign Het
Zyg11a G A 4: 108,040,845 (GRCm39) P703S probably damaging Het
Other mutations in Or7g29
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01150:Or7g29 APN 9 19,286,535 (GRCm39) missense probably damaging 1.00
IGL01293:Or7g29 APN 9 19,286,632 (GRCm39) missense probably benign 0.23
IGL01879:Or7g29 APN 9 19,286,703 (GRCm39) nonsense probably null
IGL03298:Or7g29 APN 9 19,286,358 (GRCm39) missense probably damaging 1.00
R1350:Or7g29 UTSW 9 19,286,710 (GRCm39) missense possibly damaging 0.94
R1400:Or7g29 UTSW 9 19,286,358 (GRCm39) missense probably damaging 0.98
R2894:Or7g29 UTSW 9 19,286,588 (GRCm39) nonsense probably null
R4468:Or7g29 UTSW 9 19,286,944 (GRCm39) missense probably benign 0.00
R4694:Or7g29 UTSW 9 19,286,694 (GRCm39) missense probably damaging 1.00
R4791:Or7g29 UTSW 9 19,287,105 (GRCm39) missense probably benign 0.28
R4794:Or7g29 UTSW 9 19,286,841 (GRCm39) missense probably benign 0.00
R5517:Or7g29 UTSW 9 19,287,063 (GRCm39) missense probably damaging 1.00
R5599:Or7g29 UTSW 9 19,286,925 (GRCm39) missense possibly damaging 0.77
R5777:Or7g29 UTSW 9 19,287,014 (GRCm39) missense probably benign 0.29
R6505:Or7g29 UTSW 9 19,286,237 (GRCm39) makesense probably null
R6509:Or7g29 UTSW 9 19,286,439 (GRCm39) missense probably benign
R7246:Or7g29 UTSW 9 19,286,761 (GRCm39) nonsense probably null
R7659:Or7g29 UTSW 9 19,286,854 (GRCm39) missense probably benign 0.03
R7886:Or7g29 UTSW 9 19,287,202 (GRCm39) splice site probably null
R8948:Or7g29 UTSW 9 19,286,262 (GRCm39) missense probably benign 0.03
R9326:Or7g29 UTSW 9 19,286,346 (GRCm39) missense probably damaging 1.00
R9612:Or7g29 UTSW 9 19,286,677 (GRCm39) missense possibly damaging 0.69
R9784:Or7g29 UTSW 9 19,287,116 (GRCm39) missense probably damaging 0.99
R9798:Or7g29 UTSW 9 19,286,577 (GRCm39) missense probably benign 0.30
Z1088:Or7g29 UTSW 9 19,286,980 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TGCCTCTATGGAAGACATGAAC -3'
(R):5'- CAAGCTTGCCTGTTCTGATAC -3'

Sequencing Primer
(F):5'- GCCTCTATGGAAGACATGAACTACTC -3'
(R):5'- GCAACATTTATATTTGGTGGAATTCC -3'
Posted On 2019-11-26