Incidental Mutation 'IGL01469:Or1o11'
ID 88209
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or1o11
Ensembl Gene ENSMUSG00000059687
Gene Name olfactory receptor family 1 subfamily O member 11
Synonyms MOR156-5, GA_x6K02T2PSCP-1893605-1894534, Olfr108
Accession Numbers
Essential gene? Probably non essential (E-score: 0.050) question?
Stock # IGL01469
Quality Score
Status
Chromosome 17
Chromosomal Location 37756371-37757408 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 37756426 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Threonine at position 5 (S5T)
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
AA Change: S5T
Predicted Effect probably benign
Transcript: ENSMUST00000218675
AA Change: S5T

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
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: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl4fm1 A G 4: 144,255,192 (GRCm39) Q204R possibly damaging Het
Actn2 C T 13: 12,325,796 (GRCm39) E60K possibly damaging Het
Alpk1 T C 3: 127,471,401 (GRCm39) probably null Het
Ccdc107 A G 4: 43,495,751 (GRCm39) N218S probably benign Het
Cdh23 A T 10: 60,433,504 (GRCm39) M60K probably benign Het
Cenpe A G 3: 134,934,567 (GRCm39) Q378R probably damaging Het
Dnaaf6rt A T 1: 31,262,510 (GRCm39) D164V probably damaging Het
Dnah8 T A 17: 30,902,688 (GRCm39) probably benign Het
Eif2b4 T C 5: 31,345,111 (GRCm39) D190G probably benign Het
Fmo5 A G 3: 97,558,884 (GRCm39) N448S probably benign Het
Gal3st2c A G 1: 93,937,039 (GRCm39) N328S probably benign Het
Gbf1 A T 19: 46,267,803 (GRCm39) E1271V probably damaging Het
Ifitm6 A T 7: 140,596,725 (GRCm39) V16D probably damaging Het
Ighv2-4 A G 12: 113,616,966 (GRCm39) probably null Het
Kng2 T A 16: 22,818,577 (GRCm39) K305I probably damaging Het
Lrp1 C T 10: 127,420,283 (GRCm39) R900Q probably damaging Het
Maml1 A G 11: 50,157,353 (GRCm39) M274T probably damaging Het
Med23 A G 10: 24,758,495 (GRCm39) E278G probably damaging Het
Myo1h A G 5: 114,499,330 (GRCm39) T164A probably damaging Het
Ncoa2 A T 1: 13,257,093 (GRCm39) S135R probably benign Het
Nrbf2 A G 10: 67,105,919 (GRCm39) L41P probably damaging Het
Or10a48 A G 7: 108,424,534 (GRCm39) V224A probably benign Het
Or1j13 T C 2: 36,369,836 (GRCm39) Y102C probably benign Het
Or52e5 T A 7: 104,719,595 (GRCm39) M307K probably benign Het
Or6c6 A G 10: 129,186,449 (GRCm39) M6V probably benign Het
Otoa T C 7: 120,754,496 (GRCm39) probably null Het
Plxnb1 T C 9: 108,934,483 (GRCm39) probably benign Het
Ppp1r42 A T 1: 10,073,458 (GRCm39) probably null Het
Rad54l2 T A 9: 106,599,957 (GRCm39) K100M probably damaging Het
Rnf112 T A 11: 61,342,167 (GRCm39) T308S possibly damaging Het
Scaper T C 9: 55,767,051 (GRCm39) D466G probably damaging Het
Sgsm2 T A 11: 74,744,697 (GRCm39) I796L possibly damaging Het
Shank3 T C 15: 89,405,477 (GRCm39) L476P probably damaging Het
Shkbp1 T C 7: 27,055,366 (GRCm39) T6A probably benign Het
Slc14a2 A T 18: 78,198,781 (GRCm39) I783N probably damaging Het
Stat1 A G 1: 52,186,529 (GRCm39) D447G possibly damaging Het
Tekt3 T G 11: 62,964,294 (GRCm39) I208S probably damaging Het
Tenm3 A T 8: 48,689,458 (GRCm39) V2043E probably damaging Het
Tgm3 T C 2: 129,866,414 (GRCm39) Y111H probably damaging Het
Tph2 T A 10: 114,915,664 (GRCm39) R459* probably null Het
Vmn2r109 T C 17: 20,761,671 (GRCm39) Y562C probably damaging Het
Other mutations in Or1o11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01370:Or1o11 APN 17 37,756,605 (GRCm39) missense probably benign 0.44
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
R3076:Or1o11 UTSW 17 37,756,375 (GRCm39) start gained probably benign
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
Posted On 2013-11-18