Incidental Mutation 'IGL02710:Or11g2'
ID 304517
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 # IGL02710
Quality Score
Status
Chromosome 14
Chromosomal Location 50855681-50856652 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 50856255 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Isoleucine at position 192 (T192I)
Ref Sequence ENSEMBL: ENSMUSP00000148954 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000066457] [ENSMUST00000213668] [ENSMUST00000216690]
AlphaFold Q7TRM0
Predicted Effect probably benign
Transcript: ENSMUST00000066457
AA Change: T192I

PolyPhen 2 Score 0.016 (Sensitivity: 0.95; Specificity: 0.79)
SMART Domains Protein: ENSMUSP00000066496
Gene: ENSMUSG00000053815
AA Change: T192I

DomainStartEndE-ValueType
Pfam:7tm_4 35 312 2.9e-48 PFAM
Pfam:7tm_1 45 294 1.4e-19 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000213668
AA Change: T192I

PolyPhen 2 Score 0.016 (Sensitivity: 0.95; Specificity: 0.79)
Predicted Effect probably benign
Transcript: ENSMUST00000216690
AA Change: T192I

PolyPhen 2 Score 0.016 (Sensitivity: 0.95; Specificity: 0.79)
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: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aox1 T G 1: 58,373,928 (GRCm39) probably null Het
Col18a1 G A 10: 76,949,146 (GRCm39) A122V possibly damaging Het
Dnai3 A T 3: 145,753,903 (GRCm39) I719N possibly damaging Het
Dtnb T A 12: 3,698,380 (GRCm39) H289Q possibly damaging Het
Fat4 A T 3: 38,944,744 (GRCm39) K1212N probably damaging Het
Gm10392 T C 11: 77,409,294 (GRCm39) H44R possibly damaging Het
Herc2 G A 7: 55,787,562 (GRCm39) A1740T possibly damaging Het
Ifna1 A G 4: 88,768,523 (GRCm39) D67G probably benign Het
Knl1 A C 2: 118,901,411 (GRCm39) E1037D probably damaging Het
Lsg1 A T 16: 30,390,292 (GRCm39) D274E probably benign Het
Msantd3 A G 4: 48,552,686 (GRCm39) K92E probably damaging Het
Nap1l4 G A 7: 143,077,998 (GRCm39) T312I probably benign Het
Nlrp3 A G 11: 59,456,802 (GRCm39) E988G probably damaging Het
Palm3 C T 8: 84,754,941 (GRCm39) T151I possibly damaging Het
Pde1b T C 15: 103,430,484 (GRCm39) W144R probably damaging Het
Piezo2 A G 18: 63,207,730 (GRCm39) L1427P probably damaging Het
Rasal1 A T 5: 120,804,496 (GRCm39) H456L possibly damaging Het
Sec16a C T 2: 26,320,142 (GRCm39) G1432D possibly damaging Het
Shc1 A G 3: 89,331,917 (GRCm39) probably null Het
Skint5 T A 4: 113,335,156 (GRCm39) I1452F unknown Het
Slc35b4 C A 6: 34,135,476 (GRCm39) V279L probably benign Het
Snx9 T C 17: 5,958,873 (GRCm39) V283A probably damaging Het
Stra6l T C 4: 45,882,728 (GRCm39) F480L possibly damaging Het
Stt3a A G 9: 36,670,041 (GRCm39) Y132H probably damaging Het
Sv2c T A 13: 96,125,649 (GRCm39) I363F probably damaging Het
Tnfrsf21 C T 17: 43,398,820 (GRCm39) T642I probably damaging Het
Tubgcp2 G A 7: 139,584,897 (GRCm39) probably benign Het
Usp47 A G 7: 111,692,132 (GRCm39) N845D probably benign Het
Wdr20 A T 12: 110,759,544 (GRCm39) probably benign Het
Zfp518b A G 5: 38,830,061 (GRCm39) V648A probably damaging Het
Zfp687 A T 3: 94,916,084 (GRCm39) S927T probably benign Het
Other mutations in Or11g2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01373:Or11g2 APN 14 50,856,069 (GRCm39) missense probably damaging 1.00
IGL02136:Or11g2 APN 14 50,855,708 (GRCm39) missense possibly damaging 0.86
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
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