Incidental Mutation 'R6092:Or5g29'
ID 485965
Institutional Source Beutler Lab
Gene Symbol Or5g29
Ensembl Gene ENSMUSG00000111454
Gene Name olfactory receptor family 5 subfamily G member 29
Synonyms Olfr998, GA_x6K02T2Q125-47069356-47070300, MOR175-5
MMRRC Submission 044249-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.264) question?
Stock # R6092 (G1)
Quality Score 225.009
Status Validated
Chromosome 2
Chromosomal Location 85420854-85421865 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 85420950 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Cysteine at position 22 (Y22C)
Ref Sequence ENSEMBL: ENSMUSP00000150713 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000052307] [ENSMUST00000215083]
AlphaFold Q8VF76
Predicted Effect probably benign
Transcript: ENSMUST00000052307
AA Change: Y22C

PolyPhen 2 Score 0.141 (Sensitivity: 0.92; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000059970
Gene: ENSMUSG00000111454
AA Change: Y22C

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 2.6e-54 PFAM
Pfam:7tm_1 41 308 9.5e-18 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000117353
Predicted Effect probably benign
Transcript: ENSMUST00000215083
AA Change: Y22C

PolyPhen 2 Score 0.141 (Sensitivity: 0.92; Specificity: 0.86)
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.0%
  • 20x: 94.1%
Validation Efficiency 98% (61/62)
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: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110002E22Rik C T 3: 137,774,701 (GRCm39) P1297S probably benign Het
4930486L24Rik C T 13: 61,001,461 (GRCm39) V89M probably benign Het
Abhd16a T C 17: 35,317,786 (GRCm39) probably null Het
Abtb1 A C 6: 88,815,433 (GRCm39) C264G probably benign Het
Ank3 G A 10: 69,838,395 (GRCm39) R1566K possibly damaging Het
Arid1a C T 4: 133,421,163 (GRCm39) G881R unknown Het
Asb8 A G 15: 98,034,123 (GRCm39) V144A possibly damaging Het
Atm A C 9: 53,435,714 (GRCm39) C199G probably damaging Het
Atxn1 C A 13: 45,720,288 (GRCm39) V536L probably benign Het
Baz1a C T 12: 54,955,868 (GRCm39) V1074M possibly damaging Het
BC034090 T A 1: 155,100,659 (GRCm39) D535V probably damaging Het
Casp8ap2 C A 4: 32,639,380 (GRCm39) H145N probably damaging Het
Ccdc24 T A 4: 117,729,645 (GRCm39) K25* probably null Het
Ccdc91 A G 6: 147,437,114 (GRCm39) N100S possibly damaging Het
Cdh20 A T 1: 110,026,036 (GRCm39) Y424F probably benign Het
Clasp1 T C 1: 118,438,028 (GRCm39) S612P probably damaging Het
Cxcl14 T C 13: 56,443,646 (GRCm39) M55V possibly damaging Het
Dnah11 T C 12: 117,892,191 (GRCm39) T3661A probably benign Het
Dnah14 T A 1: 181,449,398 (GRCm39) D574E probably benign Het
Dnah6 C T 6: 73,091,680 (GRCm39) V2204M possibly damaging Het
Ercc4 A T 16: 12,943,125 (GRCm39) H178L probably benign Het
Far2 T C 6: 148,076,581 (GRCm39) F475L probably benign Het
Ggt7 A G 2: 155,359,959 (GRCm39) probably null Het
Gm4131 T A 14: 62,718,364 (GRCm39) T81S possibly damaging Het
Gprc6a A G 10: 51,491,173 (GRCm39) S788P probably damaging Het
Hmgxb3 C A 18: 61,270,672 (GRCm39) G884V possibly damaging Het
Homer1 T A 13: 93,502,945 (GRCm39) probably benign Het
Iars1 T C 13: 49,861,897 (GRCm39) S483P probably damaging Het
Kansl1l C G 1: 66,812,643 (GRCm39) E457Q probably damaging Het
Krtap4-9 G A 11: 99,676,481 (GRCm39) probably benign Het
Lepr C A 4: 101,649,220 (GRCm39) P874T probably damaging Het
Mad2l2 T A 4: 148,228,067 (GRCm39) F100L probably damaging Het
Mavs A T 2: 131,087,518 (GRCm39) R339* probably null Het
Mettl1 G A 10: 126,877,843 (GRCm39) probably benign Het
Mfsd8 A G 3: 40,774,031 (GRCm39) V493A possibly damaging Het
Mtmr9 C T 14: 63,779,901 (GRCm39) V63M possibly damaging Het
Mto1 T C 9: 78,368,131 (GRCm39) I425T possibly damaging Het
Or2av9 A T 11: 58,380,900 (GRCm39) M227K probably damaging Het
Or8b36 ATTGCTGTTT ATTGCTGTTTGCTGTTT 9: 37,937,836 (GRCm39) probably null Het
Pclo C T 5: 14,727,937 (GRCm39) probably benign Het
Phf2 T C 13: 48,969,533 (GRCm39) D608G unknown Het
Plch2 T C 4: 155,068,829 (GRCm39) T1266A probably benign Het
Prdm12 A G 2: 31,533,889 (GRCm39) N169D probably damaging Het
Rimbp3 A G 16: 17,030,134 (GRCm39) Y1186C probably damaging Het
Serpinb3d T C 1: 107,006,989 (GRCm39) M240V probably damaging Het
Slc25a38 C T 9: 119,945,658 (GRCm39) R74C probably damaging Het
Slc25a39 A T 11: 102,295,719 (GRCm39) Y109* probably null Het
Slc26a8 T C 17: 28,867,129 (GRCm39) N564S probably damaging Het
Spag4 G A 2: 155,907,696 (GRCm39) probably benign Het
Stx1b A G 7: 127,407,035 (GRCm39) M74T possibly damaging Het
Tbc1d1 A G 5: 64,507,242 (GRCm39) D1153G probably benign Het
Tert T C 13: 73,776,700 (GRCm39) F484L probably benign Het
Tet1 A G 10: 62,649,494 (GRCm39) V72A probably benign Het
Tnfrsf13c T C 15: 82,107,355 (GRCm39) T147A probably damaging Het
Trpa1 A T 1: 14,959,710 (GRCm39) Y659N probably damaging Het
Trpm2 A G 10: 77,761,516 (GRCm39) F1045L probably benign Het
Ttc13 T C 8: 125,405,772 (GRCm39) H529R probably benign Het
Ttn T C 2: 76,545,614 (GRCm39) T32570A probably damaging Het
Uba7 A G 9: 107,860,359 (GRCm39) T892A possibly damaging Het
Uty A T Y: 1,174,836 (GRCm39) M195K probably benign Het
Zfp109 A G 7: 23,928,978 (GRCm39) S152P possibly damaging Het
Zfp532 T C 18: 65,777,281 (GRCm39) V846A probably damaging Het
Zfp658 A T 7: 43,223,951 (GRCm39) H742L possibly damaging Het
Zfp831 C A 2: 174,547,299 (GRCm39) P1494Q probably damaging Het
Other mutations in Or5g29
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01763:Or5g29 APN 2 85,421,691 (GRCm39) missense probably benign 0.00
R0091:Or5g29 UTSW 2 85,421,696 (GRCm39) missense probably benign 0.38
R0241:Or5g29 UTSW 2 85,421,154 (GRCm39) missense probably benign 0.20
R0241:Or5g29 UTSW 2 85,421,154 (GRCm39) missense probably benign 0.20
R0268:Or5g29 UTSW 2 85,421,645 (GRCm39) missense possibly damaging 0.78
R0481:Or5g29 UTSW 2 85,421,448 (GRCm39) missense possibly damaging 0.94
R1816:Or5g29 UTSW 2 85,421,269 (GRCm39) missense probably benign 0.00
R1988:Or5g29 UTSW 2 85,420,985 (GRCm39) missense probably benign 0.00
R2008:Or5g29 UTSW 2 85,421,766 (GRCm39) missense probably damaging 1.00
R2060:Or5g29 UTSW 2 85,421,627 (GRCm39) missense possibly damaging 0.78
R2273:Or5g29 UTSW 2 85,420,932 (GRCm39) missense probably damaging 1.00
R4409:Or5g29 UTSW 2 85,421,274 (GRCm39) missense probably damaging 1.00
R4783:Or5g29 UTSW 2 85,421,282 (GRCm39) missense probably benign 0.03
R4785:Or5g29 UTSW 2 85,421,282 (GRCm39) missense probably benign 0.03
R5098:Or5g29 UTSW 2 85,420,976 (GRCm39) missense probably benign 0.00
R5176:Or5g29 UTSW 2 85,421,779 (GRCm39) missense possibly damaging 0.88
R5462:Or5g29 UTSW 2 85,421,640 (GRCm39) missense probably damaging 1.00
R6278:Or5g29 UTSW 2 85,421,342 (GRCm39) missense probably benign 0.00
R7022:Or5g29 UTSW 2 85,420,942 (GRCm39) missense probably benign 0.01
R7673:Or5g29 UTSW 2 85,421,406 (GRCm39) missense possibly damaging 0.75
R8054:Or5g29 UTSW 2 85,421,184 (GRCm39) missense probably damaging 1.00
R8118:Or5g29 UTSW 2 85,421,332 (GRCm39) nonsense probably null
R8940:Or5g29 UTSW 2 85,421,528 (GRCm39) missense probably benign
R9617:Or5g29 UTSW 2 85,421,279 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TCTTTGTGGGGAGAGTCACC -3'
(R):5'- CACAGAGCATCTTAGGAGCTATGG -3'

Sequencing Primer
(F):5'- GACCCTGTACCCAAGATTATACATG -3'
(R):5'- GCATCTTAGGAGCTATGGAAGAAG -3'
Posted On 2017-08-16