Incidental Mutation 'IGL02136:Or11g2'
ID 281312
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or11g2
Ensembl Gene ENSMUSG00000053815
Gene Name olfactory receptor family 11 subfamily G member 2
Synonyms MOR106-13P, GA_x6K02T2PMLR-6326342-6327313, Olfr744
Accession Numbers
Essential gene? Probably non essential (E-score: 0.093) question?
Stock # IGL02136
Quality Score
Chromosome 14
Chromosomal Location 50855681-50856652 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 50855708 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 10 (S10P)
Ref Sequence ENSEMBL: ENSMUSP00000148954 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000066457] [ENSMUST00000213668] [ENSMUST00000216690]
AlphaFold Q7TRM0
Predicted Effect possibly damaging
Transcript: ENSMUST00000066457
AA Change: S10P

PolyPhen 2 Score 0.857 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000066496
Gene: ENSMUSG00000053815
AA Change: S10P

Pfam:7tm_4 35 312 2.9e-48 PFAM
Pfam:7tm_1 45 294 1.4e-19 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000213668
AA Change: S10P

PolyPhen 2 Score 0.857 (Sensitivity: 0.83; Specificity: 0.93)
Predicted Effect possibly damaging
Transcript: ENSMUST00000216690
AA Change: S10P

PolyPhen 2 Score 0.857 (Sensitivity: 0.83; Specificity: 0.93)
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: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca12 G T 1: 71,286,301 (GRCm39) T2511K probably damaging Het
Acta2 T A 19: 34,229,230 (GRCm39) D53V probably damaging Het
Banf1 G A 19: 5,415,098 (GRCm39) A71V probably benign Het
Cacng5 A T 11: 107,772,557 (GRCm39) I97N probably benign Het
Clec14a T A 12: 58,315,415 (GRCm39) E69V probably damaging Het
Cracr2a T C 6: 127,606,893 (GRCm39) probably benign Het
Dysf A G 6: 84,085,149 (GRCm39) R845G probably benign Het
Dzip3 T C 16: 48,747,945 (GRCm39) N949S possibly damaging Het
Eprs1 T G 1: 185,117,180 (GRCm39) W408G probably damaging Het
Fgf14 G A 14: 124,217,784 (GRCm39) P240S possibly damaging Het
Fpgt G T 3: 154,798,989 (GRCm39) A2E probably benign Het
Galntl5 T A 5: 25,425,060 (GRCm39) S392R probably benign Het
Gatd1 A G 7: 140,988,873 (GRCm39) *221Q probably null Het
Gcsam T A 16: 45,430,896 (GRCm39) M1K probably null Het
Ksr2 A G 5: 117,754,959 (GRCm39) N351S possibly damaging Het
Map1a T C 2: 121,130,693 (GRCm39) V503A probably damaging Het
Myl12a T A 17: 71,303,851 (GRCm39) K9* probably null Het
Ncapg2 A T 12: 116,424,203 (GRCm39) M1129L probably benign Het
Or8k41 T C 2: 86,313,809 (GRCm39) I92M probably damaging Het
Otof T C 5: 30,531,336 (GRCm39) K1691E possibly damaging Het
Pdk4 A T 6: 5,486,715 (GRCm39) M353K probably damaging Het
Pkhd1 A T 1: 20,345,839 (GRCm39) W2730R probably damaging Het
Pkn2 T A 3: 142,559,351 (GRCm39) K58I probably damaging Het
Plk5 T C 10: 80,199,001 (GRCm39) probably null Het
Prkcq T C 2: 11,265,479 (GRCm39) F399L probably benign Het
Ptprz1 G A 6: 22,972,821 (GRCm39) V244M probably damaging Het
Rpusd2 T C 2: 118,868,659 (GRCm39) F361L probably damaging Het
Rttn T A 18: 89,064,252 (GRCm39) L1168I possibly damaging Het
S100a9 T C 3: 90,600,075 (GRCm39) H107R probably benign Het
Serpinb3a T A 1: 106,974,015 (GRCm39) M299L probably benign Het
Slfn8 G A 11: 82,894,291 (GRCm39) Q783* probably null Het
Smc3 T C 19: 53,624,147 (GRCm39) I721T probably benign Het
Top2b C A 14: 16,407,103 (GRCm38) probably benign Het
Uvssa T A 5: 33,549,192 (GRCm39) W351R probably damaging Het
Vmn2r107 G T 17: 20,595,168 (GRCm39) V574L probably benign Het
Wdr3 G A 3: 100,046,041 (GRCm39) R931* probably null Het
Other mutations in Or11g2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01373:Or11g2 APN 14 50,856,069 (GRCm39) missense probably damaging 1.00
IGL02165:Or11g2 APN 14 50,856,468 (GRCm39) missense probably damaging 1.00
IGL02207:Or11g2 APN 14 50,856,015 (GRCm39) missense probably damaging 1.00
IGL02556:Or11g2 APN 14 50,856,185 (GRCm39) missense probably benign 0.01
IGL02710:Or11g2 APN 14 50,856,255 (GRCm39) missense probably benign 0.02
R0127:Or11g2 UTSW 14 50,855,789 (GRCm39) missense probably benign
R0389:Or11g2 UTSW 14 50,856,036 (GRCm39) missense probably damaging 1.00
R0603:Or11g2 UTSW 14 50,855,967 (GRCm39) missense probably damaging 1.00
R0927:Or11g2 UTSW 14 50,856,044 (GRCm39) missense possibly damaging 0.47
R1477:Or11g2 UTSW 14 50,856,170 (GRCm39) missense probably damaging 0.98
R1705:Or11g2 UTSW 14 50,856,579 (GRCm39) missense probably benign 0.01
R1800:Or11g2 UTSW 14 50,856,143 (GRCm39) missense probably benign 0.01
R1898:Or11g2 UTSW 14 50,856,231 (GRCm39) missense probably damaging 1.00
R2244:Or11g2 UTSW 14 50,856,114 (GRCm39) missense probably damaging 1.00
R4731:Or11g2 UTSW 14 50,856,026 (GRCm39) missense probably benign 0.11
R4732:Or11g2 UTSW 14 50,856,026 (GRCm39) missense probably benign 0.11
R4733:Or11g2 UTSW 14 50,856,026 (GRCm39) missense probably benign 0.11
R4801:Or11g2 UTSW 14 50,856,479 (GRCm39) missense probably benign 0.01
R4802:Or11g2 UTSW 14 50,856,479 (GRCm39) missense probably benign 0.01
R5068:Or11g2 UTSW 14 50,856,197 (GRCm39) missense probably damaging 1.00
R5069:Or11g2 UTSW 14 50,856,197 (GRCm39) missense probably damaging 1.00
R5070:Or11g2 UTSW 14 50,856,197 (GRCm39) missense probably damaging 1.00
R5070:Or11g2 UTSW 14 50,855,931 (GRCm39) missense probably benign 0.11
R5195:Or11g2 UTSW 14 50,856,243 (GRCm39) missense probably damaging 1.00
R6058:Or11g2 UTSW 14 50,856,158 (GRCm39) missense probably benign 0.03
R8246:Or11g2 UTSW 14 50,855,841 (GRCm39) missense probably benign
R8275:Or11g2 UTSW 14 50,855,868 (GRCm39) missense probably damaging 1.00
R9292:Or11g2 UTSW 14 50,856,513 (GRCm39) missense possibly damaging 0.94
Posted On 2015-04-16