Incidental Mutation 'R5101:Or4x11'
ID 392343
Institutional Source Beutler Lab
Gene Symbol Or4x11
Ensembl Gene ENSMUSG00000059910
Gene Name olfactory receptor family 4 subfamily X member 11
Synonyms MOR228-2, GA_x6K02T2Q125-51469027-51469956, Olfr1265
MMRRC Submission 042852-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.065) question?
Stock # R5101 (G1)
Quality Score 225
Status Validated
Chromosome 2
Chromosomal Location 89867265-89868194 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 89867391 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Valine at position 43 (M43V)
Ref Sequence ENSEMBL: ENSMUSP00000149684 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080311] [ENSMUST00000214855]
AlphaFold Q8VEZ3
Predicted Effect probably benign
Transcript: ENSMUST00000080311
AA Change: M43V

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000079190
Gene: ENSMUSG00000059910
AA Change: M43V

DomainStartEndE-ValueType
Pfam:7tm_4 29 303 1.9e-49 PFAM
Pfam:7tm_1 39 285 1.4e-20 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000214855
AA Change: M43V

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.3%
  • 10x: 96.4%
  • 20x: 93.0%
Validation Efficiency 100% (57/57)
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: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam17 T C 12: 21,423,406 (GRCm39) T10A possibly damaging Het
Adgrg3 T C 8: 95,763,563 (GRCm39) F288S probably benign Het
Ago2 A G 15: 72,991,339 (GRCm39) V533A probably damaging Het
Akap9 T G 5: 4,051,748 (GRCm39) V1505G probably damaging Het
Apob T C 12: 8,061,934 (GRCm39) I3439T probably benign Het
C1qtnf7 T A 5: 43,773,314 (GRCm39) Y204* probably null Het
Cdc42bpb T C 12: 111,265,549 (GRCm39) E1461G probably damaging Het
Cdh3 C T 8: 107,268,024 (GRCm39) A353V possibly damaging Het
Clec4d A G 6: 123,244,071 (GRCm39) Y60C probably damaging Het
Cmya5 T A 13: 93,228,111 (GRCm39) T2326S possibly damaging Het
Cnot1 G A 8: 96,486,815 (GRCm39) L631F possibly damaging Het
Cntnap5a C T 1: 116,370,026 (GRCm39) T881I probably benign Het
Col6a1 T A 10: 76,545,740 (GRCm39) T911S unknown Het
Ctsw A G 19: 5,515,703 (GRCm39) V287A probably benign Het
Cyp2c23 T C 19: 44,017,622 (GRCm39) E2G unknown Het
Cytip A T 2: 58,037,911 (GRCm39) I151N probably damaging Het
Dnah10 A G 5: 124,909,577 (GRCm39) T4399A possibly damaging Het
Dock3 A T 9: 106,846,980 (GRCm39) I883N probably damaging Het
Entpd3 A G 9: 120,395,608 (GRCm39) *530W probably null Het
Gm4787 G C 12: 81,424,604 (GRCm39) T518S probably benign Het
Gp1ba G A 11: 70,532,225 (GRCm39) V664M probably benign Het
Gpd2 T A 2: 57,245,913 (GRCm39) I481N probably damaging Het
Gvin-ps5 T C 7: 105,929,096 (GRCm39) noncoding transcript Het
Ildr2 A G 1: 166,135,331 (GRCm39) D342G probably damaging Het
Krt87 A G 15: 101,385,391 (GRCm39) I327T probably benign Het
Lats1 T A 10: 7,588,348 (GRCm39) C988* probably null Het
Lpin2 G A 17: 71,550,965 (GRCm39) W708* probably null Het
Mast4 T C 13: 102,872,864 (GRCm39) D2168G probably benign Het
Myo6 G T 9: 80,177,321 (GRCm39) E606* probably null Het
Nek7 A G 1: 138,443,431 (GRCm39) V174A probably benign Het
Nid1 T A 13: 13,658,339 (GRCm39) C695S probably damaging Het
Nme8 A G 13: 19,875,017 (GRCm39) probably null Het
Nr2c2 T C 6: 92,131,497 (GRCm39) probably null Het
Or1e16 AGCGGTCGTAGGC AGC 11: 73,286,480 (GRCm39) probably null Het
Or2ag18 A T 7: 106,405,420 (GRCm39) I83K possibly damaging Het
Or51ab3 G A 7: 103,201,150 (GRCm39) E53K probably damaging Het
Or9g19 A G 2: 85,600,268 (GRCm39) N41S probably damaging Het
Pms2 A G 5: 143,865,006 (GRCm39) D696G probably damaging Het
Psapl1 T A 5: 36,361,494 (GRCm39) C29S probably damaging Het
Scn3a A T 2: 65,291,850 (GRCm39) V1632D probably damaging Het
Slc22a1 C T 17: 12,886,129 (GRCm39) G168D probably damaging Het
Smad4 A G 18: 73,808,931 (GRCm39) V112A probably benign Het
Smc4 T C 3: 68,935,845 (GRCm39) V796A probably benign Het
Smco4 A G 9: 15,455,968 (GRCm39) E18G unknown Het
Spata31e2 T C 1: 26,722,417 (GRCm39) E921G possibly damaging Het
Sugp2 A G 8: 70,713,139 (GRCm39) E1035G probably damaging Het
Syde2 T C 3: 145,721,393 (GRCm39) S820P probably damaging Het
Syn2 T C 6: 115,240,860 (GRCm39) L410P probably damaging Het
Tmem131l T C 3: 83,844,811 (GRCm39) N466S probably damaging Het
Uba1y T G Y: 821,447 (GRCm39) probably null Het
Unc79 T C 12: 103,078,769 (GRCm39) S1645P probably damaging Het
Vmn2r17 A T 5: 109,576,217 (GRCm39) S363C probably damaging Het
Vmn2r78 T C 7: 86,571,563 (GRCm39) Y458H probably damaging Het
Other mutations in Or4x11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01154:Or4x11 APN 2 89,867,812 (GRCm39) missense probably damaging 1.00
IGL01470:Or4x11 APN 2 89,868,162 (GRCm39) missense possibly damaging 0.81
IGL01878:Or4x11 APN 2 89,867,478 (GRCm39) missense probably damaging 0.97
IGL02716:Or4x11 APN 2 89,868,138 (GRCm39) missense probably benign 0.05
IGL03066:Or4x11 APN 2 89,867,778 (GRCm39) missense probably damaging 0.99
R1310:Or4x11 UTSW 2 89,868,047 (GRCm39) missense probably benign 0.02
R4986:Or4x11 UTSW 2 89,867,772 (GRCm39) missense probably damaging 1.00
R6149:Or4x11 UTSW 2 89,867,860 (GRCm39) missense probably benign 0.01
R6400:Or4x11 UTSW 2 89,867,739 (GRCm39) missense probably benign 0.00
R7367:Or4x11 UTSW 2 89,868,156 (GRCm39) missense probably benign 0.02
R7432:Or4x11 UTSW 2 89,867,528 (GRCm39) missense probably damaging 0.99
R7645:Or4x11 UTSW 2 89,868,091 (GRCm39) missense possibly damaging 0.90
R7849:Or4x11 UTSW 2 89,867,626 (GRCm39) missense probably damaging 1.00
R9265:Or4x11 UTSW 2 89,867,842 (GRCm39) missense probably benign 0.01
R9634:Or4x11 UTSW 2 89,867,907 (GRCm39) missense probably damaging 1.00
R9756:Or4x11 UTSW 2 89,867,674 (GRCm39) missense probably benign 0.02
X0019:Or4x11 UTSW 2 89,867,988 (GRCm39) missense probably benign 0.02
Predicted Primers PCR Primer
(F):5'- CTTGGATCAAGGTTTTCTGCAAAAG -3'
(R):5'- GTGCATGAAGAAAAGCTGTGTC -3'

Sequencing Primer
(F):5'- CTCATGGCTGACATACAC -3'
(R):5'- TGTGTCATGCAGCCCCATACAG -3'
Posted On 2016-06-15