Incidental Mutation 'R3076:Or1o11'
ID 265238
Institutional Source Beutler Lab
Gene Symbol Or1o11
Ensembl Gene ENSMUSG00000059687
Gene Name olfactory receptor family 1 subfamily O member 11
Synonyms MOR156-5, GA_x6K02T2PSCP-1893605-1894534, Olfr108
MMRRC Submission 040566-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.050) question?
Stock # R3076 (G1)
Quality Score 225
Status Not validated
Chromosome 17
Chromosomal Location 37756371-37757408 bp(+) (GRCm39)
Type of Mutation start gained
DNA Base Change (assembly) T to C at 37756375 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000151360 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000078207] [ENSMUST00000207414] [ENSMUST00000218675]
AlphaFold Q8VFA1
Predicted Effect probably benign
Transcript: ENSMUST00000078207
SMART Domains Protein: ENSMUSP00000077337
Gene: ENSMUSG00000059687

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srv 33 315 8.8e-9 PFAM
Pfam:7tm_4 39 316 9.5e-54 PFAM
Pfam:7tm_1 49 298 1.8e-19 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000207414
Predicted Effect probably benign
Transcript: ENSMUST00000218675
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.4%
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: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrd1 A T 5: 129,206,169 (GRCm39) I248F probably benign Het
Amigo2 C T 15: 97,143,315 (GRCm39) R369Q probably damaging Het
Aopep A C 13: 63,387,929 (GRCm39) D3A probably damaging Het
Arfgef3 T C 10: 18,479,278 (GRCm39) I1446V probably damaging Het
Ascc2 T A 11: 4,622,446 (GRCm39) L504Q probably damaging Het
Atp1a3 A G 7: 24,679,498 (GRCm39) V932A possibly damaging Het
Cabcoco1 T G 10: 68,361,475 (GRCm39) Y8S possibly damaging Het
Cct8 A G 16: 87,285,765 (GRCm39) V231A possibly damaging Het
Col18a1 T C 10: 76,924,762 (GRCm39) K9R possibly damaging Het
Dlgap3 A G 4: 127,089,499 (GRCm39) Y365C probably damaging Het
Dock3 T C 9: 106,818,725 (GRCm39) probably null Het
Gtf3c4 A T 2: 28,725,165 (GRCm39) V189E possibly damaging Het
Khdc3 C A 9: 73,010,212 (GRCm39) F89L probably damaging Het
Kif14 T G 1: 136,447,383 (GRCm39) I1396S possibly damaging Het
Magi1 T C 6: 93,734,668 (GRCm39) Q393R possibly damaging Het
Med28 A G 5: 45,679,820 (GRCm39) T68A possibly damaging Het
Meis1 A T 11: 18,961,254 (GRCm39) N206K probably benign Het
Mnt G C 11: 74,733,936 (GRCm39) probably benign Het
Mrgpre C T 7: 143,335,033 (GRCm39) A157T probably benign Het
Mtpn C T 6: 35,498,879 (GRCm39) V76I possibly damaging Het
Nbeal2 A T 9: 110,460,768 (GRCm39) W1702R probably damaging Het
Nhsl2 C T X: 101,121,201 (GRCm39) R62W probably damaging Het
Npr2 T A 4: 43,640,182 (GRCm39) Y306N probably damaging Het
Nrsn1 T C 13: 25,437,542 (GRCm39) T129A probably benign Het
Nrxn3 T G 12: 89,227,186 (GRCm39) C274G probably damaging Het
Nyap2 T C 1: 81,219,686 (GRCm39) probably null Het
Or1e29 G A 11: 73,667,466 (GRCm39) P229L possibly damaging Het
Phldb2 T C 16: 45,645,373 (GRCm39) T403A probably benign Het
Plaa T C 4: 94,458,042 (GRCm39) I643V probably benign Het
Ptprb T C 10: 116,179,931 (GRCm39) S1450P probably damaging Het
Sh2d2a T C 3: 87,759,477 (GRCm39) I296T probably benign Het
Shtn1 T C 19: 58,983,518 (GRCm39) E471G probably damaging Het
St7 T G 6: 17,846,237 (GRCm39) Y163* probably null Het
Svil T C 18: 5,116,055 (GRCm39) S1623P probably damaging Het
Ugcg T G 4: 59,213,922 (GRCm39) V168G probably damaging Het
Vmn1r223 G A 13: 23,434,335 (GRCm39) A310T probably benign Het
Zfp647 A T 15: 76,802,209 (GRCm39) M1K probably null Het
Other mutations in Or1o11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01370:Or1o11 APN 17 37,756,605 (GRCm39) missense probably benign 0.44
IGL01469:Or1o11 APN 17 37,756,426 (GRCm39) missense probably benign 0.00
IGL02291:Or1o11 APN 17 37,757,176 (GRCm39) missense possibly damaging 0.62
IGL02892:Or1o11 APN 17 37,756,925 (GRCm39) missense probably damaging 1.00
IGL03390:Or1o11 APN 17 37,757,255 (GRCm39) missense probably benign 0.02
R0115:Or1o11 UTSW 17 37,756,670 (GRCm39) missense probably benign 0.00
R0395:Or1o11 UTSW 17 37,756,757 (GRCm39) missense probably damaging 1.00
R0427:Or1o11 UTSW 17 37,756,593 (GRCm39) missense probably damaging 0.99
R0557:Or1o11 UTSW 17 37,756,712 (GRCm39) missense probably damaging 1.00
R1709:Or1o11 UTSW 17 37,757,091 (GRCm39) nonsense probably null
R5467:Or1o11 UTSW 17 37,756,973 (GRCm39) missense probably damaging 1.00
R5642:Or1o11 UTSW 17 37,756,663 (GRCm39) missense probably damaging 1.00
R5916:Or1o11 UTSW 17 37,756,570 (GRCm39) missense probably benign 0.16
R7451:Or1o11 UTSW 17 37,757,196 (GRCm39) missense probably damaging 1.00
R8205:Or1o11 UTSW 17 37,757,180 (GRCm39) missense probably damaging 1.00
R8280:Or1o11 UTSW 17 37,756,744 (GRCm39) missense probably benign 0.11
R9748:Or1o11 UTSW 17 37,756,595 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- GCCTTTGAAGGGATCACAGTC -3'
(R):5'- GTCCCAGCAAGTAAAGACCTAGG -3'

Sequencing Primer
(F):5'- CCTTTGAAGGGATCACAGTCAAACAG -3'
(R):5'- GAAGATGATAAAGAAGTGCTGCCAC -3'
Posted On 2015-02-05