Incidental Mutation 'R7886:Or7g29'
ID 628699
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 045938-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.132) question?
Stock # R7886 (G1)
Quality Score 225.009
Status Validated
Chromosome 9
Chromosomal Location 19286237-19287175 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 19287202 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000151112 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000079620] [ENSMUST00000216839]
AlphaFold Q8VFF4
Predicted Effect probably benign
Transcript: ENSMUST00000079620
SMART Domains Protein: ENSMUSP00000078568
Gene: ENSMUSG00000059821

Pfam:7tm_4 31 308 1.9e-56 PFAM
Pfam:7tm_1 41 290 2.1e-22 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000216839
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.9%
Validation Efficiency 100% (53/53)
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: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A730049H05Rik T G 6: 92,811,437 (GRCm39) I130S unknown Het
Ano5 A G 7: 51,220,141 (GRCm39) H427R probably benign Het
Atad2 A T 15: 57,989,532 (GRCm39) V182E probably damaging Het
B4galnt1 T C 10: 127,002,923 (GRCm39) Y147H probably damaging Het
C1s2 T C 6: 124,605,289 (GRCm39) S349G possibly damaging Het
Ccdc51 G T 9: 108,920,655 (GRCm39) A181S probably damaging Het
Dcc G A 18: 72,087,939 (GRCm39) Q100* probably null Het
Dchs2 A T 3: 83,212,392 (GRCm39) I2064F probably damaging Het
Depdc1a G A 3: 159,221,706 (GRCm39) V217I probably benign Het
Dnajc7 A T 11: 100,492,629 (GRCm39) F31I probably benign Het
Eftud2 C T 11: 102,730,934 (GRCm39) R825H probably damaging Het
Fam184a T C 10: 53,551,256 (GRCm39) E237G probably damaging Het
Fdx2 A T 9: 20,984,623 (GRCm39) probably null Het
Frem1 T C 4: 82,934,643 (GRCm39) D106G possibly damaging Het
Gabrg3 G A 7: 56,374,229 (GRCm39) R446W probably damaging Het
Get1 T A 16: 95,946,768 (GRCm39) L31Q possibly damaging Het
Gm42669 A G 5: 107,656,572 (GRCm39) E362G Het
Hmcn1 A T 1: 150,533,221 (GRCm39) I3022N possibly damaging Het
Ifna2 C A 4: 88,601,506 (GRCm39) V171F probably damaging Het
Igsf10 T C 3: 59,235,748 (GRCm39) N1478D probably benign Het
Kcnc1 C A 7: 46,077,045 (GRCm39) D282E probably damaging Het
Klhdc2 G A 12: 69,351,406 (GRCm39) probably null Het
Macrod2 G A 2: 141,566,565 (GRCm39) G188S probably damaging Het
Mapkbp1 T C 2: 119,843,128 (GRCm39) F186L possibly damaging Het
Mettl21a T C 1: 64,654,343 (GRCm39) E58G probably damaging Het
Muc16 A T 9: 18,497,278 (GRCm39) C6625S probably benign Het
Naip5 A T 13: 100,382,689 (GRCm39) S7T probably benign Het
Nfs1 T A 2: 155,983,981 (GRCm39) D132V unknown Het
Nlgn1 T C 3: 25,490,071 (GRCm39) D552G probably damaging Het
Numa1 C T 7: 101,663,072 (GRCm39) T2066I probably benign Het
Or10k2 T C 8: 84,268,576 (GRCm39) S268P possibly damaging Het
Or2t48 C A 11: 58,419,880 (GRCm39) V311L probably benign Het
Or4k2 A T 14: 50,424,021 (GRCm39) Y219N probably damaging Het
Or7a39 A G 10: 78,715,657 (GRCm39) Y217C possibly damaging Het
Pde11a C T 2: 76,121,547 (GRCm39) V345I probably benign Het
Pglyrp2 A G 17: 32,637,735 (GRCm39) S98P possibly damaging Het
Pik3c3 C T 18: 30,452,641 (GRCm39) Q643* probably null Het
Pold2 T C 11: 5,822,714 (GRCm39) Y402C probably damaging Het
Pom121 T C 5: 135,410,848 (GRCm39) T770A unknown Het
Pou4f1 A T 14: 104,704,228 (GRCm39) V68E probably damaging Het
Ppfia1 G T 7: 144,073,020 (GRCm39) Q265K probably benign Het
Pygl A G 12: 70,253,130 (GRCm39) probably null Het
Rdh19 A G 10: 127,686,169 (GRCm39) T94A probably benign Het
Scgb1b12 A G 7: 32,033,922 (GRCm39) T61A probably damaging Het
Sirpb1c C T 3: 15,886,366 (GRCm39) A337T probably benign Het
Sltm C G 9: 70,493,955 (GRCm39) P802R possibly damaging Het
Tbc1d23 T C 16: 57,009,746 (GRCm39) E381G possibly damaging Het
Tnik A G 3: 28,720,288 (GRCm39) I1304V probably damaging Het
Tpmt C A 13: 47,193,638 (GRCm39) G54C probably damaging Het
Usp25 A T 16: 76,910,659 (GRCm39) Q905L probably damaging Het
Vmn1r91 T A 7: 19,835,490 (GRCm39) N136K probably benign Het
Wdr70 C T 15: 8,108,733 (GRCm39) E138K probably benign Het
Zbed3 A G 13: 95,472,633 (GRCm39) D19G possibly damaging Het
Zfp369 A G 13: 65,439,868 (GRCm39) K184R possibly 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
R7789:Or7g29 UTSW 9 19,286,361 (GRCm39) missense probably benign 0.33
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

Sequencing Primer
Posted On 2020-06-10