Incidental Mutation 'R1626:Or7g32'
ID 172505
Institutional Source Beutler Lab
Gene Symbol Or7g32
Ensembl Gene ENSMUSG00000052625
Gene Name olfactory receptor family 7 subfamily G member 32
Synonyms MOR155-1, GA_x6K02T2PVTD-13234278-13235216, Olfr851
MMRRC Submission 039663-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.127) question?
Stock # R1626 (G1)
Quality Score 225
Status Not validated
Chromosome 9
Chromosomal Location 19404591-19414111 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 19389495 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Proline at position 14 (L14P)
Ref Sequence ENSEMBL: ENSMUSP00000148623 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000077347] [ENSMUST00000211832]
AlphaFold Q7TRG0
Predicted Effect probably damaging
Transcript: ENSMUST00000077347
AA Change: L17P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000076569
Gene: ENSMUSG00000094535
AA Change: L17P

DomainStartEndE-ValueType
low complexity region 10 21 N/A INTRINSIC
Pfam:7tm_4 34 311 1.8e-51 PFAM
Pfam:7TM_GPCR_Srsx 38 304 1e-6 PFAM
Pfam:7tm_1 44 293 5.1e-24 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000211832
AA Change: L14P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.1%
  • 10x: 95.5%
  • 20x: 90.1%
Validation Efficiency
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
1700020N01Rik T C 10: 21,497,571 (GRCm39) Y71H possibly damaging Het
Acsl6 C A 11: 54,242,872 (GRCm39) P628T probably damaging Het
Ak7 A G 12: 105,734,807 (GRCm39) D591G probably benign Het
Anxa5 T C 3: 36,516,130 (GRCm39) D66G probably damaging Het
Cacna1b G A 2: 24,496,721 (GRCm39) T2283I probably damaging Het
Cand1 A T 10: 119,045,919 (GRCm39) D995E possibly damaging Het
Cblc G T 7: 19,530,427 (GRCm39) A94E probably damaging Het
Cd48 G A 1: 171,509,687 (GRCm39) C9Y probably benign Het
Chd9 A G 8: 91,721,224 (GRCm39) K1004R probably benign Het
Cilk1 A G 9: 78,057,919 (GRCm39) Y156C probably damaging Het
Cldn1 T C 16: 26,190,202 (GRCm39) T59A probably damaging Het
Col11a1 G A 3: 113,925,218 (GRCm39) G17D probably damaging Het
Cpeb1 A G 7: 81,085,995 (GRCm39) V49A probably damaging Het
Cyp4b1 G T 4: 115,498,855 (GRCm39) P109Q probably damaging Het
Dhrs7b T A 11: 60,735,082 (GRCm39) F23I possibly damaging Het
Dnah9 C A 11: 65,976,093 (GRCm39) A1319S probably benign Het
Egf A T 3: 129,479,864 (GRCm39) V553D possibly damaging Het
Fbn1 T C 2: 125,183,199 (GRCm39) D1760G probably damaging Het
Fbxo31 A G 8: 122,286,745 (GRCm39) F178L probably damaging Het
Fstl4 C A 11: 52,891,117 (GRCm39) S85* probably null Het
Gfm1 A G 3: 67,345,977 (GRCm39) Y225C probably damaging Het
Gm10797 A T 10: 67,408,453 (GRCm39) noncoding transcript Het
H3c8 G A 13: 23,719,721 (GRCm39) V36M probably damaging Het
Heatr4 T A 12: 84,020,495 (GRCm39) I499L probably benign Het
Igfn1 A T 1: 135,896,705 (GRCm39) M1287K probably benign Het
Inpp5b C A 4: 124,677,696 (GRCm39) D385E probably damaging Het
Lrrc9 A G 12: 72,542,435 (GRCm39) probably null Het
Ltb4r1 A G 14: 56,004,699 (GRCm39) M1V probably null Het
Macf1 T C 4: 123,365,327 (GRCm39) I3145V probably benign Het
Man2a2 T C 7: 80,017,450 (GRCm39) N277S probably damaging Het
Megf6 G T 4: 154,261,578 (GRCm39) V68L probably benign Het
Mgat4e A G 1: 134,469,016 (GRCm39) Y343H probably benign Het
Noxred1 T C 12: 87,268,029 (GRCm39) *367W probably null Het
Nup58 A T 14: 60,480,076 (GRCm39) L190* probably null Het
Olfml2a G T 2: 38,841,275 (GRCm39) K270N probably damaging Het
Or5c1 A G 2: 37,222,774 (GRCm39) probably null Het
Phgdh G T 3: 98,223,725 (GRCm39) Q359K probably benign Het
Plpp5 G T 8: 26,212,604 (GRCm39) C200F possibly damaging Het
Pole A C 5: 110,441,235 (GRCm39) I230L probably benign Het
Prtg A T 9: 72,752,193 (GRCm39) D193V probably damaging Het
Ptgs2 G A 1: 149,979,619 (GRCm39) probably null Het
Ptprz1 A T 6: 23,001,573 (GRCm39) Q1221L probably benign Het
Rufy2 T C 10: 62,831,151 (GRCm39) I204T probably benign Het
Rybp A G 6: 100,209,919 (GRCm39) S115P possibly damaging Het
Samd13 A G 3: 146,368,481 (GRCm39) V37A probably benign Het
Secisbp2l T G 2: 125,617,606 (GRCm39) K24Q probably damaging Het
Sorbs2 A G 8: 46,222,891 (GRCm39) Y198C probably damaging Het
Svil T G 18: 5,117,099 (GRCm39) probably null Het
Ttc24 G T 3: 87,977,366 (GRCm39) R127S probably benign Het
Ttn C T 2: 76,588,888 (GRCm39) V21394M probably damaging Het
Tubal3 G T 13: 3,982,841 (GRCm39) C207F probably damaging Het
Vmn2r16 A T 5: 109,511,443 (GRCm39) D550V probably damaging Het
Vmn2r2 T A 3: 64,041,921 (GRCm39) I265F possibly damaging Het
Zfp507 T C 7: 35,494,858 (GRCm39) K62E probably damaging Het
Other mutations in Or7g32
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00094:Or7g32 APN 9 19,408,155 (GRCm39) missense probably damaging 1.00
IGL01992:Or7g32 APN 9 19,408,070 (GRCm39) missense probably benign 0.00
IGL02455:Or7g32 APN 9 19,408,559 (GRCm39) nonsense probably null
IGL02468:Or7g32 APN 9 19,408,473 (GRCm39) missense probably benign
IGL02685:Or7g32 APN 9 19,408,098 (GRCm39) missense probably benign
IGL02723:Or7g32 APN 9 19,388,805 (GRCm39) missense probably damaging 1.00
IGL03294:Or7g32 APN 9 19,389,285 (GRCm39) missense possibly damaging 0.95
PIT4305001:Or7g32 UTSW 9 19,389,357 (GRCm39) missense probably damaging 1.00
R0153:Or7g32 UTSW 9 19,408,233 (GRCm39) missense probably damaging 1.00
R0364:Or7g32 UTSW 9 19,389,268 (GRCm39) nonsense probably null
R0379:Or7g32 UTSW 9 19,388,776 (GRCm39) missense possibly damaging 0.75
R0449:Or7g32 UTSW 9 19,389,388 (GRCm39) missense possibly damaging 0.89
R0682:Or7g32 UTSW 9 19,388,645 (GRCm39) missense probably benign 0.03
R0693:Or7g32 UTSW 9 19,389,268 (GRCm39) nonsense probably null
R0789:Or7g32 UTSW 9 19,408,458 (GRCm39) missense possibly damaging 0.68
R1484:Or7g32 UTSW 9 19,389,423 (GRCm39) missense probably damaging 1.00
R1599:Or7g32 UTSW 9 19,389,517 (GRCm39) missense probably damaging 0.97
R1742:Or7g32 UTSW 9 19,389,337 (GRCm39) missense probably damaging 1.00
R2041:Or7g32 UTSW 9 19,408,131 (GRCm39) missense probably benign
R2060:Or7g32 UTSW 9 19,408,533 (GRCm39) missense possibly damaging 0.88
R4232:Or7g32 UTSW 9 19,389,022 (GRCm39) missense probably damaging 0.98
R4237:Or7g32 UTSW 9 19,388,893 (GRCm39) missense probably benign 0.00
R4474:Or7g32 UTSW 9 19,408,173 (GRCm39) missense probably damaging 1.00
R5081:Or7g32 UTSW 9 19,408,557 (GRCm39) missense probably benign 0.05
R5116:Or7g32 UTSW 9 19,389,094 (GRCm39) missense possibly damaging 0.67
R5643:Or7g32 UTSW 9 19,388,853 (GRCm39) missense probably benign 0.22
R6271:Or7g32 UTSW 9 19,389,337 (GRCm39) missense probably damaging 1.00
R6815:Or7g32 UTSW 9 19,389,061 (GRCm39) missense probably benign 0.20
R6853:Or7g32 UTSW 9 19,408,102 (GRCm39) nonsense probably null
R7150:Or7g32 UTSW 9 19,408,145 (GRCm39) missense probably benign 0.44
R7222:Or7g32 UTSW 9 19,388,763 (GRCm39) missense probably damaging 1.00
R7378:Or7g32 UTSW 9 19,408,398 (GRCm39) missense probably damaging 1.00
R7456:Or7g32 UTSW 9 19,408,844 (GRCm39) missense probably damaging 1.00
R7527:Or7g32 UTSW 9 19,408,685 (GRCm39) missense probably damaging 0.98
R7587:Or7g32 UTSW 9 19,408,818 (GRCm39) missense probably damaging 1.00
R7592:Or7g32 UTSW 9 19,389,128 (GRCm39) missense possibly damaging 0.52
R8155:Or7g32 UTSW 9 19,389,453 (GRCm39) missense probably benign 0.17
R8215:Or7g32 UTSW 9 19,408,796 (GRCm39) missense probably damaging 1.00
R8220:Or7g32 UTSW 9 19,408,317 (GRCm39) missense probably damaging 0.97
R8296:Or7g32 UTSW 9 19,408,377 (GRCm39) missense probably damaging 1.00
R8732:Or7g32 UTSW 9 19,408,098 (GRCm39) missense probably benign
R8813:Or7g32 UTSW 9 19,389,477 (GRCm39) missense possibly damaging 0.75
R9152:Or7g32 UTSW 9 19,408,448 (GRCm39) missense probably damaging 1.00
R9187:Or7g32 UTSW 9 19,389,166 (GRCm39) missense probably benign
R9528:Or7g32 UTSW 9 19,389,444 (GRCm39) missense probably damaging 1.00
R9789:Or7g32 UTSW 9 19,389,382 (GRCm39) missense probably benign 0.35
R9795:Or7g32 UTSW 9 19,408,412 (GRCm39) missense probably damaging 1.00
RF034:Or7g32 UTSW 9 19,388,928 (GRCm39) missense possibly damaging 0.46
X0058:Or7g32 UTSW 9 19,389,519 (GRCm39) missense probably benign 0.10
Z1177:Or7g32 UTSW 9 19,388,633 (GRCm39) frame shift probably null
Predicted Primers PCR Primer
(F):5'- CCAGCATCTTTGGGATCGTGCTTG -3'
(R):5'- GCTGGGAGGCAGTCTGTGATAATC -3'

Sequencing Primer
(F):5'- ATCGTGCTTGTGCTTAAACAG -3'
(R):5'- catcctgatctttatgctggtttc -3'
Posted On 2014-04-24