Incidental Mutation 'IGL01926:Olfr1109'
ID180307
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Olfr1109
Ensembl Gene ENSMUSG00000075161
Gene Nameolfactory receptor 1109
SynonymsMOR172-5, GA_x6K02T2Q125-48586461-48585523
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.065) question?
Stock #IGL01926
Quality Score
Status
Chromosome2
Chromosomal Location87091195-87096008 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to T at 87092974 bp
ZygosityHeterozygous
Amino Acid Change Cysteine to Tyrosine at position 141 (C141Y)
Ref Sequence ENSEMBL: ENSMUSP00000149282 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099863] [ENSMUST00000214636] [ENSMUST00000217066]
Predicted Effect probably damaging
Transcript: ENSMUST00000099863
AA Change: C141Y

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000097449
Gene: ENSMUSG00000075161
AA Change: C141Y

DomainStartEndE-ValueType
Pfam:7tm_4 31 307 8.3e-52 PFAM
Pfam:7tm_1 41 290 6.1e-21 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000214636
AA Change: C141Y

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000217066
AA Change: C141Y

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
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
Abca9 C T 11: 110,135,329 probably benign Het
Ano1 C T 7: 144,610,875 V671M possibly damaging Het
Atf7ip2 G T 16: 10,241,885 D430Y probably damaging Het
Atp7b A T 8: 22,011,781 D740E probably damaging Het
Bbs1 A C 19: 4,902,863 S191A probably benign Het
Capn5 C T 7: 98,128,472 probably null Het
Cyp2c40 A G 19: 39,802,655 I244T probably benign Het
Dsg1a G T 18: 20,333,584 D504Y possibly damaging Het
Eif3a T C 19: 60,769,961 D793G unknown Het
Exoc4 C A 6: 33,862,142 D704E probably damaging Het
Fmo5 A C 3: 97,637,481 T109P probably damaging Het
Ggt5 A G 10: 75,604,101 I179V probably benign Het
Gm10718 A T 9: 3,025,118 Y194F probably benign Het
Gm21738 G A 14: 19,416,979 S144L probably benign Het
Irs1 G T 1: 82,289,959 R179S probably damaging Het
Jmy A T 13: 93,459,786 V445E probably damaging Het
Jup C A 11: 100,383,586 V93F probably benign Het
Krt20 T C 11: 99,437,826 Y91C probably damaging Het
Mug2 T A 6: 122,036,104 probably benign Het
Mybpc3 C T 2: 91,135,407 T1188I possibly damaging Het
Myt1 T C 2: 181,821,997 L1032P probably benign Het
Naip6 A T 13: 100,300,196 N606K probably damaging Het
Nfrkb A T 9: 31,414,179 M973L probably benign Het
Olfr1477 A T 19: 13,502,741 T133S possibly damaging Het
Parp8 T C 13: 116,862,302 probably benign Het
Plekha5 T A 6: 140,525,916 M131K probably benign Het
Pomt1 T A 2: 32,243,472 S207T probably benign Het
Prlr T A 15: 10,314,220 M1K probably null Het
Prr15 A G 6: 54,329,505 K83E probably damaging Het
Rnf4 A G 5: 34,346,779 N5S probably benign Het
Sel1l3 T A 5: 53,200,143 H169L probably benign Het
Slc24a5 A G 2: 125,068,903 I85V probably benign Het
Tmc2 T C 2: 130,260,240 I775T possibly damaging Het
Trnau1ap A T 4: 132,319,562 F141L probably benign Het
Zscan4d A G 7: 11,164,994 C119R probably damaging Het
Zswim9 A T 7: 13,260,321 V636D possibly damaging Het
Other mutations in Olfr1109
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01341:Olfr1109 APN 2 87093299 missense probably benign
IGL03195:Olfr1109 APN 2 87092569 missense probably damaging 1.00
R0550:Olfr1109 UTSW 2 87093129 missense probably benign 0.00
R1334:Olfr1109 UTSW 2 87093227 missense probably damaging 0.98
R1677:Olfr1109 UTSW 2 87092737 missense probably benign
R1753:Olfr1109 UTSW 2 87093227 missense probably damaging 0.98
R3933:Olfr1109 UTSW 2 87092762 missense probably benign 0.01
R4151:Olfr1109 UTSW 2 87093170 missense probably benign 0.07
R4296:Olfr1109 UTSW 2 87092630 missense probably benign 0.00
R6654:Olfr1109 UTSW 2 87093050 missense probably benign 0.23
R6657:Olfr1109 UTSW 2 87093059 missense probably benign 0.00
R7697:Olfr1109 UTSW 2 87092818 missense probably benign 0.30
R8178:Olfr1109 UTSW 2 87092876 missense possibly damaging 0.94
R8413:Olfr1109 UTSW 2 87093158 missense probably benign 0.25
Z1176:Olfr1109 UTSW 2 87093224 missense possibly damaging 0.87
Posted On2014-05-07