Incidental Mutation 'R0364:Or7g32'
ID 30234
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 038570-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.342) question?
Stock # R0364 (G1)
Quality Score 225
Status Validated
Chromosome 9
Chromosomal Location 19404591-19414111 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to A at 19389268 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Stop codon at position 90 (Q90*)
Ref Sequence ENSEMBL: ENSMUSP00000148623 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000077347] [ENSMUST00000211832]
AlphaFold Q7TRG0
Predicted Effect probably null
Transcript: ENSMUST00000077347
AA Change: Q93*
SMART Domains Protein: ENSMUSP00000076569
Gene: ENSMUSG00000094535
AA Change: Q93*

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 null
Transcript: ENSMUST00000211832
AA Change: Q90*
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.0%
  • 10x: 95.3%
  • 20x: 89.3%
Validation Efficiency 99% (86/87)
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: 87 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acp7 G A 7: 28,310,553 (GRCm39) probably benign Het
Ano7 A G 1: 93,316,380 (GRCm39) D221G probably benign Het
Arhgef12 A T 9: 42,929,697 (GRCm39) N199K probably damaging Het
Arpc2 A G 1: 74,276,046 (GRCm39) N26S probably null Het
Camta2 G A 11: 70,574,136 (GRCm39) T127I probably damaging Het
Ccdc13 T A 9: 121,627,282 (GRCm39) N665I probably damaging Het
Ccdc178 C T 18: 22,048,119 (GRCm39) R757H probably damaging Het
Cfap52 A C 11: 67,844,436 (GRCm39) I93S possibly damaging Het
Cmklr1 A T 5: 113,752,578 (GRCm39) L141H probably damaging Het
Crybb3 T A 5: 113,223,819 (GRCm39) I197F probably damaging Het
Cryzl1 G A 16: 91,504,155 (GRCm39) P97S probably benign Het
Cubn T C 2: 13,315,318 (GRCm39) probably benign Het
Cyp2d37-ps T C 15: 82,574,253 (GRCm39) noncoding transcript Het
Cyp4a12b C A 4: 115,290,117 (GRCm39) N223K probably benign Het
Dennd2a T C 6: 39,485,233 (GRCm39) T349A probably benign Het
Dnah12 A G 14: 26,445,628 (GRCm39) T730A probably benign Het
Dock5 G A 14: 68,060,129 (GRCm39) probably benign Het
Dync2i1 A G 12: 116,221,097 (GRCm39) probably benign Het
Elac2 A G 11: 64,870,136 (GRCm39) Y67C probably damaging Het
Elmo1 A T 13: 20,748,663 (GRCm39) K503* probably null Het
Endou A T 15: 97,616,854 (GRCm39) probably benign Het
Eng T C 2: 32,569,149 (GRCm39) S559P probably benign Het
Epc2 T A 2: 49,427,145 (GRCm39) V563E possibly damaging Het
Fbxw17 T C 13: 50,586,477 (GRCm39) S40P possibly damaging Het
Flt4 A T 11: 49,527,818 (GRCm39) M924L probably benign Het
Fyb1 A G 15: 6,610,272 (GRCm39) K282E probably damaging Het
Gabpa T A 16: 84,654,275 (GRCm39) N317K possibly damaging Het
Gli3 G T 13: 15,899,349 (GRCm39) G912V probably benign Het
Gm10295 C A 7: 71,000,361 (GRCm39) C73F unknown Het
Gm10382 G T 5: 125,466,728 (GRCm39) probably benign Het
Gp1ba T C 11: 70,531,284 (GRCm39) probably benign Het
Gpr146 G A 5: 139,364,933 (GRCm39) probably benign Het
Grm5 A G 7: 87,723,594 (GRCm39) Y628C probably damaging Het
Hexa A G 9: 59,471,218 (GRCm39) N491D probably benign Het
Hexd T A 11: 121,102,969 (GRCm39) H62Q probably benign Het
Hpx G T 7: 105,245,471 (GRCm39) Q101K probably benign Het
Ino80 G A 2: 119,213,441 (GRCm39) R1249C probably damaging Het
Inpp4b A T 8: 82,723,943 (GRCm39) T492S probably benign Het
Iqgap2 A C 13: 95,867,783 (GRCm39) probably benign Het
Islr2 T C 9: 58,107,027 (GRCm39) T78A possibly damaging Het
Itga9 A G 9: 118,670,210 (GRCm39) T177A probably benign Het
Itpkc A C 7: 26,927,174 (GRCm39) S247A possibly damaging Het
Kirrel1 T C 3: 86,997,106 (GRCm39) Y287C probably damaging Het
Kiz T G 2: 146,784,076 (GRCm39) S536R probably benign Het
Klhl9 T G 4: 88,638,527 (GRCm39) K571N probably benign Het
Kprp A T 3: 92,731,642 (GRCm39) Y469* probably null Het
Ksr1 A T 11: 78,919,851 (GRCm39) probably benign Het
Lrrc37a C T 11: 103,391,466 (GRCm39) V1320I possibly damaging Het
Ltf A T 9: 110,854,235 (GRCm39) N350I probably benign Het
Msl3l2 G A 10: 55,991,947 (GRCm39) R224Q possibly damaging Het
Myh6 A T 14: 55,185,804 (GRCm39) Y1490* probably null Het
Necap1 A G 6: 122,857,728 (GRCm39) probably benign Het
Nf1 A T 11: 79,332,783 (GRCm39) K810* probably null Het
Nkx6-3 A G 8: 23,647,722 (GRCm39) E227G possibly damaging Het
Nlrp1a T A 11: 71,004,830 (GRCm39) probably benign Het
Obscn G A 11: 59,019,107 (GRCm39) A969V probably benign Het
Or11a4 T C 17: 37,536,934 (GRCm39) L306P possibly damaging Het
Or8b40 A G 9: 38,027,325 (GRCm39) T78A probably benign Het
Or8k33 A T 2: 86,384,123 (GRCm39) L115Q probably damaging Het
Pcdhb17 C A 18: 37,618,888 (GRCm39) A226E possibly damaging Het
Phldb1 A T 9: 44,610,632 (GRCm39) probably benign Het
Plekha5 G A 6: 140,537,473 (GRCm39) R646K possibly damaging Het
Pon2 G A 6: 5,266,156 (GRCm39) Q288* probably null Het
Prr14 G A 7: 127,073,751 (GRCm39) R205H probably benign Het
Ptpn13 C A 5: 103,681,214 (GRCm39) R805S probably damaging Het
Pyroxd2 A T 19: 42,735,992 (GRCm39) V62D probably damaging Het
Rab37 G T 11: 115,047,790 (GRCm39) C44F probably damaging Het
Rbm44 T C 1: 91,080,069 (GRCm39) S52P probably benign Het
Rusf1 C T 7: 127,889,786 (GRCm39) R1H probably damaging Het
Scn5a T C 9: 119,351,665 (GRCm39) D772G probably damaging Het
Slc7a5 A G 8: 122,611,754 (GRCm39) F425L probably benign Het
Slk T A 19: 47,608,628 (GRCm39) L527* probably null Het
Stpg4 T A 17: 87,697,142 (GRCm39) probably null Het
Taar6 C A 10: 23,861,046 (GRCm39) V167L probably benign Het
Tas2r123 T A 6: 132,824,644 (GRCm39) S180R probably benign Het
Tmc2 C T 2: 130,044,023 (GRCm39) R86W probably benign Het
Tmem200c T A 17: 69,147,543 (GRCm39) V42E probably damaging Het
Trhde T C 10: 114,338,887 (GRCm39) probably benign Het
Tshz1 A T 18: 84,034,249 (GRCm39) I53N probably benign Het
Tshz3 A G 7: 36,469,958 (GRCm39) E649G probably benign Het
Ttll7 C A 3: 146,650,936 (GRCm39) R719S possibly damaging Het
Utp4 T C 8: 107,625,169 (GRCm39) probably benign Het
Vmn1r35 A G 6: 66,655,827 (GRCm39) I281T probably damaging Het
Vps39 T G 2: 120,176,119 (GRCm39) K76T probably damaging Het
Whamm A G 7: 81,243,799 (GRCm39) T674A probably benign Het
Zbtb16 A G 9: 48,654,876 (GRCm39) probably benign Het
Zfp623 T C 15: 75,820,510 (GRCm39) S489P probably benign 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
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
R1626:Or7g32 UTSW 9 19,389,495 (GRCm39) missense probably damaging 1.00
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'- CAGGGTTCCATGATGACTGTGTACC -3'
(R):5'- TAAGTCTCTCAGGGACATGCCTGC -3'

Sequencing Primer
(F):5'- GAGACAGTTTTCCATGCCAC -3'
(R):5'- catcctgatctttatgctggtttc -3'
Posted On 2013-04-24