Incidental Mutation 'IGL01461:Or7e165'
ID 87974
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or7e165
Ensembl Gene ENSMUSG00000058659
Gene Name olfactory receptor family 7 subfamily E member 165
Synonyms Olfr58, MOR146-7P, IG6, GA_x6K02T2PVTD-13523015-13523944, MOR146-3
Accession Numbers
Essential gene? Probably non essential (E-score: 0.059) question?
Stock # IGL01461
Quality Score
Status
Chromosome 9
Chromosomal Location 19691579-19695360 bp(+) (GRCm39)
Type of Mutation splice site (557 bp from exon)
DNA Base Change (assembly) T to A at 19695245 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000148538 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000079660] [ENSMUST00000212363] [ENSMUST00000215112]
AlphaFold Q7TRF6
Predicted Effect probably benign
Transcript: ENSMUST00000079660
AA Change: M272K

PolyPhen 2 Score 0.028 (Sensitivity: 0.95; Specificity: 0.81)
SMART Domains Protein: ENSMUSP00000078603
Gene: ENSMUSG00000063842
AA Change: M272K

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 1.3e-51 PFAM
Pfam:7TM_GPCR_Srsx 35 303 8.3e-8 PFAM
Pfam:7tm_1 41 290 4.5e-22 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000212363
Predicted Effect probably benign
Transcript: ENSMUST00000215112
AA Change: M272K

PolyPhen 2 Score 0.028 (Sensitivity: 0.95; Specificity: 0.81)
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: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2210408I21Rik T C 13: 77,429,214 (GRCm39) F767S probably benign Het
Abca13 A G 11: 9,353,834 (GRCm39) T3719A probably damaging Het
Apob A T 12: 8,051,884 (GRCm39) M1137L probably benign Het
Brd9 C T 13: 74,099,717 (GRCm39) Q445* probably null Het
Cdh23 T C 10: 60,244,926 (GRCm39) T990A possibly damaging Het
Cenpf A G 1: 189,389,293 (GRCm39) L1513S probably damaging Het
Col27a1 A G 4: 63,142,480 (GRCm39) K56R probably damaging Het
Cryaa A G 17: 31,900,000 (GRCm39) Y118C probably damaging Het
Dtl T C 1: 191,278,729 (GRCm39) T378A possibly damaging Het
E330020D12Rik A G 1: 153,284,105 (GRCm39) noncoding transcript Het
F7 A G 8: 13,082,245 (GRCm39) D145G possibly damaging Het
Flvcr2 A G 12: 85,849,905 (GRCm39) probably benign Het
Hltf A T 3: 20,154,103 (GRCm39) K680* probably null Het
Ing1 T G 8: 11,611,453 (GRCm39) F22V probably benign Het
Ipo5 A G 14: 121,165,945 (GRCm39) D330G probably damaging Het
Itgax G T 7: 127,734,190 (GRCm39) D321Y probably damaging Het
Kel A C 6: 41,678,845 (GRCm39) probably null Het
Marchf10 T C 11: 105,280,431 (GRCm39) K618R probably damaging Het
Mast4 T A 13: 102,890,576 (GRCm39) M925L probably damaging Het
Miga1 C T 3: 152,040,934 (GRCm39) E78K probably damaging Het
Or4c106 G T 2: 88,682,669 (GRCm39) C125F probably damaging Het
Pkdrej T C 15: 85,704,575 (GRCm39) I454V possibly damaging Het
Poglut2 T C 1: 44,150,094 (GRCm39) Q365R probably damaging Het
Prpf6 C A 2: 181,273,304 (GRCm39) T283N probably benign Het
R3hdm1 A G 1: 128,106,643 (GRCm39) H197R probably damaging Het
Resf1 T C 6: 149,233,013 (GRCm39) probably benign Het
Smpd4 A C 16: 17,439,370 (GRCm39) Q7P probably damaging Het
Vmn2r84 A T 10: 130,227,094 (GRCm39) I248K possibly damaging Het
Other mutations in Or7e165
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01815:Or7e165 APN 9 19,695,311 (GRCm39) missense probably damaging 1.00
IGL02408:Or7e165 APN 9 19,694,711 (GRCm39) missense probably benign 0.31
IGL02644:Or7e165 APN 9 19,695,010 (GRCm39) missense probably benign 0.30
IGL03243:Or7e165 APN 9 19,694,564 (GRCm39) missense probably damaging 0.99
R0603:Or7e165 UTSW 9 19,695,235 (GRCm39) missense probably damaging 1.00
R2363:Or7e165 UTSW 9 19,694,892 (GRCm39) missense probably benign 0.00
R2570:Or7e165 UTSW 9 19,695,305 (GRCm39) missense probably damaging 1.00
R3890:Or7e165 UTSW 9 19,695,011 (GRCm39) missense probably benign 0.03
R3892:Or7e165 UTSW 9 19,695,011 (GRCm39) missense probably benign 0.03
R4163:Or7e165 UTSW 9 19,695,086 (GRCm39) missense possibly damaging 0.69
R4610:Or7e165 UTSW 9 19,694,442 (GRCm39) nonsense probably null
R4691:Or7e165 UTSW 9 19,694,678 (GRCm39) missense probably benign 0.33
R4707:Or7e165 UTSW 9 19,694,596 (GRCm39) missense probably damaging 1.00
R4825:Or7e165 UTSW 9 19,694,872 (GRCm39) missense possibly damaging 0.74
R4950:Or7e165 UTSW 9 19,695,027 (GRCm39) missense probably benign
R5185:Or7e165 UTSW 9 19,694,672 (GRCm39) missense probably damaging 1.00
R5202:Or7e165 UTSW 9 19,694,514 (GRCm39) missense possibly damaging 0.46
R5439:Or7e165 UTSW 9 19,695,161 (GRCm39) missense probably damaging 1.00
R5669:Or7e165 UTSW 9 19,695,053 (GRCm39) missense probably benign 0.02
R5672:Or7e165 UTSW 9 19,694,507 (GRCm39) missense possibly damaging 0.92
R6038:Or7e165 UTSW 9 19,694,858 (GRCm39) missense probably benign
R6038:Or7e165 UTSW 9 19,694,858 (GRCm39) missense probably benign
R6212:Or7e165 UTSW 9 19,694,585 (GRCm39) missense probably damaging 1.00
R6415:Or7e165 UTSW 9 19,695,044 (GRCm39) missense probably damaging 1.00
R7385:Or7e165 UTSW 9 19,694,507 (GRCm39) missense possibly damaging 0.92
R7669:Or7e165 UTSW 9 19,694,839 (GRCm39) missense possibly damaging 0.79
Posted On 2013-11-18