Incidental Mutation 'IGL02723:Or7g32'
ID 305050
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or7g32
Ensembl Gene ENSMUSG00000052625
Gene Name olfactory receptor family 7 subfamily G member 32
Synonyms MOR155-1, GA_x6K02T2PVTD-13234278-13235216, Olfr851
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.342) question?
Stock # IGL02723
Quality Score
Status
Chromosome 9
Chromosomal Location 19404591-19414111 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 19388805 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Arginine at position 244 (H244R)
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: H247R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000076569
Gene: ENSMUSG00000094535
AA Change: H247R

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: H244R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Coding Region Coverage
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: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Capn9 A T 8: 125,335,922 (GRCm39) probably benign Het
Cchcr1 A C 17: 35,841,699 (GRCm39) K761Q probably benign Het
Cfap20dc T C 14: 8,516,507 (GRCm38) N347S probably benign Het
Csk G T 9: 57,538,672 (GRCm39) probably benign Het
Cyp2j7 T C 4: 96,118,366 (GRCm39) K76E probably benign Het
Dpep1 G A 8: 123,920,888 (GRCm39) A23T possibly damaging Het
Dpp8 T A 9: 64,949,549 (GRCm39) M98K possibly damaging Het
Dspp C A 5: 104,323,041 (GRCm39) N61K probably benign Het
Eno2 T C 6: 124,738,626 (GRCm39) Y364C probably damaging Het
Gfra1 A G 19: 58,441,683 (GRCm39) S83P probably benign Het
Gramd1b T C 9: 40,218,127 (GRCm39) E563G probably damaging Het
Kcns2 G T 15: 34,838,961 (GRCm39) W108L probably damaging Het
Mroh4 T C 15: 74,480,086 (GRCm39) probably benign Het
Obscn A T 11: 59,015,446 (GRCm39) S1009T probably benign Het
Or2y11 A G 11: 49,443,506 (GRCm39) R311G probably benign Het
Or5b119 A G 19: 13,456,699 (GRCm39) Y288H probably damaging Het
Or8b41 A G 9: 38,054,707 (GRCm39) K92R probably benign Het
Plcb2 G A 2: 118,547,500 (GRCm39) probably benign Het
Rpl13a-ps1 T A 19: 50,019,111 (GRCm39) I22F possibly damaging Het
Skil A G 3: 31,171,673 (GRCm39) E599G probably damaging Het
Snx19 A G 9: 30,343,556 (GRCm39) N572S possibly damaging Het
Spata31 T C 13: 65,068,463 (GRCm39) S204P probably benign Het
Srrm1 G A 4: 135,052,415 (GRCm39) P658L unknown Het
Tenm3 A T 8: 48,729,938 (GRCm39) V1356E probably benign Het
Trpc3 T A 3: 36,704,377 (GRCm39) I527F probably benign Het
Vmn2r69 A G 7: 85,059,416 (GRCm39) W498R probably damaging Het
Vwde T A 6: 13,205,759 (GRCm39) I263L probably damaging Het
Vwf G T 6: 125,619,893 (GRCm39) V1524L possibly damaging Het
Wdr55 A G 18: 36,896,435 (GRCm39) E375G 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
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
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
Posted On 2015-04-16