Incidental Mutation 'IGL02256:Or10j2'
ID 286583
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or10j2
Ensembl Gene ENSMUSG00000049605
Gene Name olfactory receptor family 10 subfamily J member 2
Synonyms MOR267-8, Olfr418, Olfr1403, GA_x6K02T2P20D-20826777-20827719, Olfr418-ps1, MOR267-12P, GA_x6K02T2R7CC-581296-580364
Accession Numbers
Essential gene? Probably non essential (E-score: 0.092) question?
Stock # IGL02256
Quality Score
Status
Chromosome 1
Chromosomal Location 173097714-173098704 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 173098194 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 151 (I151F)
Ref Sequence ENSEMBL: ENSMUSP00000150427 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000059754] [ENSMUST00000111224] [ENSMUST00000213420]
AlphaFold A0A140T8J6
Predicted Effect probably benign
Transcript: ENSMUST00000059754
AA Change: I151F

PolyPhen 2 Score 0.038 (Sensitivity: 0.94; Specificity: 0.82)
SMART Domains Protein: ENSMUSP00000052418
Gene: ENSMUSG00000049605
AA Change: I151F

DomainStartEndE-ValueType
Pfam:7tm_4 31 307 1.6e-55 PFAM
Pfam:7tm_1 41 289 5.7e-25 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000111224
SMART Domains Protein: ENSMUSP00000106855
Gene: ENSMUSG00000079180

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
PTX 20 219 1.93e-94 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000213420
AA Change: I151F

PolyPhen 2 Score 0.038 (Sensitivity: 0.94; Specificity: 0.82)
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: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ambra1 T A 2: 91,599,399 (GRCm39) V173E possibly damaging Het
Dennd4c A G 4: 86,717,778 (GRCm39) T592A probably damaging Het
Dhcr24 G A 4: 106,429,517 (GRCm39) G197S probably damaging Het
Fat1 A G 8: 45,403,369 (GRCm39) Y40C probably damaging Het
Fbxl17 A C 17: 63,806,085 (GRCm39) C310G probably benign Het
H2bc8 G T 13: 23,755,609 (GRCm39) M1I probably null Het
Hdac10 T C 15: 89,010,097 (GRCm39) probably benign Het
Mcm6 A G 1: 128,263,465 (GRCm39) probably null Het
Mrpl19 G A 6: 81,941,300 (GRCm39) T87I probably benign Het
Mzf1 A G 7: 12,786,664 (GRCm39) probably benign Het
Nhlrc2 A G 19: 56,585,793 (GRCm39) E676G probably benign Het
Notch3 T C 17: 32,351,298 (GRCm39) D1899G probably damaging Het
Nxph1 A G 6: 9,247,185 (GRCm39) D52G probably benign Het
Or10g9b A G 9: 39,917,349 (GRCm39) F299L probably benign Het
Or2aj6 T C 16: 19,443,756 (GRCm39) I31M probably benign Het
Or2n1 G T 17: 38,486,577 (GRCm39) V201L probably benign Het
Or8b3b A T 9: 38,584,776 (GRCm39) M1K probably null Het
Or8b49 G A 9: 38,505,840 (GRCm39) V108I probably benign Het
Pax6 T C 2: 105,515,115 (GRCm39) V54A probably benign Het
Pbx1 A T 1: 168,011,171 (GRCm39) H376Q possibly damaging Het
Prpf4b T A 13: 35,083,861 (GRCm39) C877S probably damaging Het
Robo3 A G 9: 37,336,649 (GRCm39) L373P probably damaging Het
Samd9l G A 6: 3,376,197 (GRCm39) R355W probably damaging Het
Smarce1 A T 11: 99,110,206 (GRCm39) N127K possibly damaging Het
Sptbn1 T C 11: 30,070,990 (GRCm39) I1511V probably benign Het
Stab1 C T 14: 30,863,549 (GRCm39) R2071H probably damaging Het
Svep1 A T 4: 58,070,311 (GRCm39) C2492S possibly damaging Het
Tbr1 C A 2: 61,635,218 (GRCm39) T56N probably damaging Het
Thoc2l T A 5: 104,668,149 (GRCm39) Y890* probably null Het
Tlr6 T C 5: 65,112,287 (GRCm39) T207A probably benign Het
Tmem241 A G 18: 12,246,489 (GRCm39) W54R probably damaging Het
Tmem87a A G 2: 120,208,377 (GRCm39) V326A probably damaging Het
Trappc14 C A 5: 138,258,577 (GRCm39) D557Y probably damaging Het
Uroc1 A G 6: 90,323,669 (GRCm39) D372G possibly damaging Het
Zc3h7a A C 16: 10,965,140 (GRCm39) S664R probably benign Het
Other mutations in Or10j2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01413:Or10j2 APN 1 173,098,275 (GRCm39) missense probably damaging 1.00
IGL01418:Or10j2 APN 1 173,098,275 (GRCm39) missense probably damaging 1.00
IGL01930:Or10j2 APN 1 173,098,177 (GRCm39) missense probably benign
IGL01963:Or10j2 APN 1 173,097,919 (GRCm39) missense probably damaging 0.99
IGL02104:Or10j2 APN 1 173,098,603 (GRCm39) missense probably damaging 0.96
IGL02192:Or10j2 APN 1 173,098,417 (GRCm39) missense probably damaging 1.00
IGL02340:Or10j2 APN 1 173,097,972 (GRCm39) missense probably benign 0.10
IGL02454:Or10j2 APN 1 173,098,507 (GRCm39) missense probably damaging 0.99
IGL02638:Or10j2 APN 1 173,097,898 (GRCm39) missense probably benign 0.07
FR4737:Or10j2 UTSW 1 173,098,197 (GRCm39) frame shift probably null
FR4976:Or10j2 UTSW 1 173,098,197 (GRCm39) frame shift probably null
R0552:Or10j2 UTSW 1 173,098,372 (GRCm39) missense probably benign 0.05
R0621:Or10j2 UTSW 1 173,098,242 (GRCm39) missense possibly damaging 0.48
R0735:Or10j2 UTSW 1 173,098,569 (GRCm39) missense probably benign 0.05
R1506:Or10j2 UTSW 1 173,098,336 (GRCm39) missense probably benign 0.04
R1670:Or10j2 UTSW 1 173,098,467 (GRCm39) missense probably damaging 1.00
R2111:Or10j2 UTSW 1 173,097,879 (GRCm39) missense probably benign
R2204:Or10j2 UTSW 1 173,097,703 (GRCm39) splice site probably null
R4475:Or10j2 UTSW 1 173,098,480 (GRCm39) missense probably damaging 0.99
R4909:Or10j2 UTSW 1 173,098,546 (GRCm39) missense probably damaging 0.97
R5457:Or10j2 UTSW 1 173,098,141 (GRCm39) missense probably benign 0.00
R6124:Or10j2 UTSW 1 173,097,846 (GRCm39) missense probably damaging 1.00
R6456:Or10j2 UTSW 1 173,098,105 (GRCm39) missense probably damaging 1.00
R7220:Or10j2 UTSW 1 173,097,811 (GRCm39) missense possibly damaging 0.56
R7240:Or10j2 UTSW 1 173,098,561 (GRCm39) missense probably benign 0.27
R7672:Or10j2 UTSW 1 173,098,440 (GRCm39) missense probably benign 0.18
R8073:Or10j2 UTSW 1 173,098,552 (GRCm39) missense probably benign 0.42
R8116:Or10j2 UTSW 1 173,098,047 (GRCm39) missense possibly damaging 0.88
R8982:Or10j2 UTSW 1 173,098,306 (GRCm39) missense probably damaging 1.00
R9038:Or10j2 UTSW 1 173,098,147 (GRCm39) missense possibly damaging 0.63
R9668:Or10j2 UTSW 1 173,098,183 (GRCm39) missense possibly damaging 0.94
RF032:Or10j2 UTSW 1 173,098,276 (GRCm39) frame shift probably null
RF036:Or10j2 UTSW 1 173,098,276 (GRCm39) frame shift probably null
RF040:Or10j2 UTSW 1 173,098,276 (GRCm39) frame shift probably null
X0019:Or10j2 UTSW 1 173,098,124 (GRCm39) nonsense probably null
Posted On 2015-04-16