Incidental Mutation 'IGL02839:Or5t9'
ID 361785
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or5t9
Ensembl Gene ENSMUSG00000044213
Gene Name olfactory receptor family 5 subfamily T member 9
Synonyms Olfr1094, GA_x6K02T2Q125-48321457-48322449, MOR179-7
Accession Numbers
Essential gene? Probably non essential (E-score: 0.240) question?
Stock # IGL02839
Quality Score
Status
Chromosome 2
Chromosomal Location 86659020-86660166 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 86659712 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Lysine at position 205 (N205K)
Ref Sequence ENSEMBL: ENSMUSP00000148902 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000105211] [ENSMUST00000217509]
AlphaFold Q8VF13
Predicted Effect probably benign
Transcript: ENSMUST00000105211
AA Change: N205K

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000100846
Gene: ENSMUSG00000044213
AA Change: N205K

DomainStartEndE-ValueType
Pfam:7tm_4 43 320 4.6e-52 PFAM
Pfam:7tm_1 53 316 3.5e-18 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000217509
AA Change: N205K

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
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: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A3galt2 T C 4: 128,653,816 (GRCm39) probably null Het
Aldh1l1 T C 6: 90,546,857 (GRCm39) F387L possibly damaging Het
Aldh5a1 A G 13: 25,095,603 (GRCm39) S505P probably damaging Het
Aox1 A G 1: 58,107,943 (GRCm39) T642A probably benign Het
Atg16l2 T C 7: 100,942,604 (GRCm39) I364V probably damaging Het
Atp2c2 T C 8: 120,475,859 (GRCm39) V584A possibly damaging Het
Axl A T 7: 25,466,216 (GRCm39) probably null Het
Camta1 T C 4: 151,228,969 (GRCm39) Q621R probably damaging Het
Cdca4 A T 12: 112,785,511 (GRCm39) D72E probably damaging Het
Col1a2 T A 6: 4,538,748 (GRCm39) Y1223N unknown Het
Drc1 T C 5: 30,507,767 (GRCm39) M263T probably benign Het
Eef1akmt1 A T 14: 57,787,238 (GRCm39) Y213N probably damaging Het
Fat3 C A 9: 15,830,466 (GRCm39) D4343Y probably damaging Het
Ftdc1 A G 16: 58,436,210 (GRCm39) Y38H probably damaging Het
Gucy2d T C 7: 98,093,196 (GRCm39) V191A possibly damaging Het
Hdac5 A G 11: 102,095,734 (GRCm39) L355P probably damaging Het
Hdgfl3 C T 7: 81,550,160 (GRCm39) G58D probably damaging Het
Hnrnpul1 A G 7: 25,432,667 (GRCm39) probably null Het
Klf12 A T 14: 100,137,675 (GRCm39) C290* probably null Het
Mtmr3 A T 11: 4,437,994 (GRCm39) I820N probably benign Het
Myo7a A T 7: 97,740,329 (GRCm39) L555Q probably damaging Het
Nrsn1 A G 13: 25,437,527 (GRCm39) C134R probably damaging Het
Or13c7d T A 4: 43,770,943 (GRCm39) K23* probably null Het
Or1p1 T A 11: 74,180,196 (GRCm39) C241* probably null Het
Or4c11c G A 2: 88,661,992 (GRCm39) C177Y probably damaging Het
Or56a3b A C 7: 104,771,563 (GRCm39) T300P probably damaging Het
Or5ac24 A T 16: 59,165,753 (GRCm39) C104S probably benign Het
Pik3r6 A G 11: 68,417,238 (GRCm39) E60G probably damaging Het
Pkhd1l1 T A 15: 44,392,939 (GRCm39) I1758N probably damaging Het
Poc1b A G 10: 98,980,460 (GRCm39) probably benign Het
Rnf103 G T 6: 71,486,689 (GRCm39) R440L probably benign Het
Siglec1 A G 2: 130,926,852 (GRCm39) V237A possibly damaging Het
Skic2 T C 17: 35,066,774 (GRCm39) T165A probably benign Het
Slit3 A G 11: 35,539,874 (GRCm39) N762S possibly damaging Het
Trank1 A G 9: 111,193,824 (GRCm39) N616S probably damaging Het
Trav14d-3-dv8 C A 14: 53,316,247 (GRCm39) Q36K possibly damaging Het
Ttll6 T C 11: 96,049,646 (GRCm39) V788A probably damaging Het
Ube4b A T 4: 149,452,856 (GRCm39) S357T probably damaging Het
Unc80 A G 1: 66,710,834 (GRCm39) H2701R possibly damaging Het
Wdfy3 A G 5: 102,116,786 (GRCm39) S85P probably damaging Het
Other mutations in Or5t9
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03053:Or5t9 APN 2 86,659,607 (GRCm39) missense possibly damaging 0.93
IGL03168:Or5t9 APN 2 86,659,607 (GRCm39) missense possibly damaging 0.93
IGL02799:Or5t9 UTSW 2 86,659,300 (GRCm39) missense probably damaging 0.99
R0511:Or5t9 UTSW 2 86,659,950 (GRCm39) missense probably benign 0.02
R0944:Or5t9 UTSW 2 86,659,281 (GRCm39) missense probably benign 0.01
R1065:Or5t9 UTSW 2 86,659,888 (GRCm39) missense probably damaging 0.98
R1476:Or5t9 UTSW 2 86,659,542 (GRCm39) missense probably benign 0.31
R1807:Or5t9 UTSW 2 86,659,445 (GRCm39) missense probably benign 0.03
R2865:Or5t9 UTSW 2 86,659,198 (GRCm39) missense probably benign 0.21
R2915:Or5t9 UTSW 2 86,659,570 (GRCm39) missense probably benign 0.02
R3055:Or5t9 UTSW 2 86,659,471 (GRCm39) missense possibly damaging 0.94
R3104:Or5t9 UTSW 2 86,660,035 (GRCm39) missense probably benign 0.03
R4862:Or5t9 UTSW 2 86,659,876 (GRCm39) missense probably damaging 1.00
R4874:Or5t9 UTSW 2 86,659,598 (GRCm39) missense probably damaging 0.98
R5505:Or5t9 UTSW 2 86,659,845 (GRCm39) missense possibly damaging 0.88
R5507:Or5t9 UTSW 2 86,659,661 (GRCm39) missense probably damaging 1.00
R6318:Or5t9 UTSW 2 86,659,998 (GRCm39) missense possibly damaging 0.73
R6538:Or5t9 UTSW 2 86,659,869 (GRCm39) missense possibly damaging 0.55
R8058:Or5t9 UTSW 2 86,660,052 (GRCm39) missense probably benign 0.01
R8285:Or5t9 UTSW 2 86,659,443 (GRCm39) missense probably benign 0.03
R9563:Or5t9 UTSW 2 86,659,098 (GRCm39) start codon destroyed probably null 0.04
Posted On 2015-12-18