Incidental Mutation 'IGL03106:Or5t15'
ID 418947
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or5t15
Ensembl Gene ENSMUSG00000075171
Gene Name olfactory receptor family 5 subfamily T member 15
Synonyms GA_x6K02T2Q125-48336843-48335917, MOR179-1, Olfr1095
Accession Numbers
Essential gene? Probably non essential (E-score: 0.060) question?
Stock # IGL03106
Quality Score
Status
Chromosome 2
Chromosomal Location 86681114-86682040 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 86681958 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Arginine at position 28 (L28R)
Ref Sequence ENSEMBL: ENSMUSP00000097459 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099874]
AlphaFold A3KPP7
Predicted Effect possibly damaging
Transcript: ENSMUST00000099874
AA Change: L28R

PolyPhen 2 Score 0.920 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000097459
Gene: ENSMUSG00000075171
AA Change: L28R

DomainStartEndE-ValueType
Pfam:7tm_4 29 306 1.7e-47 PFAM
Pfam:7tm_1 39 288 9.8e-21 PFAM
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: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam3 G T 8: 25,205,135 (GRCm39) probably benign Het
Adgrv1 T C 13: 81,621,018 (GRCm39) N3911S probably benign Het
Alox12b C T 11: 69,059,702 (GRCm39) Q585* probably null Het
Amtn A G 5: 88,525,944 (GRCm39) Q36R probably benign Het
Arg2 G A 12: 79,196,665 (GRCm39) G129S probably damaging Het
Arhgef28 A C 13: 98,094,301 (GRCm39) Y948D probably damaging Het
Atp10b T C 11: 43,138,304 (GRCm39) V1195A probably benign Het
Bet1l G T 7: 140,434,523 (GRCm39) T42K probably benign Het
Cabin1 G A 10: 75,569,462 (GRCm39) T875I probably benign Het
Ccdc17 A G 4: 116,454,033 (GRCm39) probably null Het
Crebrf A G 17: 26,990,293 (GRCm39) E612G probably damaging Het
Cyp2c67 A T 19: 39,632,119 (GRCm39) M83K probably benign Het
Dgkz A G 2: 91,771,204 (GRCm39) S414P probably damaging Het
Dock10 G T 1: 80,546,551 (GRCm39) H411N probably damaging Het
Dpyd A T 3: 118,988,783 (GRCm39) T749S probably benign Het
Dsc1 C T 18: 20,219,701 (GRCm39) probably null Het
Echdc1 A T 10: 29,198,276 (GRCm39) M74L probably damaging Het
Edn1 C A 13: 42,458,499 (GRCm39) T104K possibly damaging Het
Fat2 T A 11: 55,202,727 (GRCm39) T116S probably benign Het
Fcrl5 A T 3: 87,343,190 (GRCm39) probably null Het
Fpgt C T 3: 154,792,759 (GRCm39) G423R probably damaging Het
Gprc5b A T 7: 118,583,416 (GRCm39) V151E probably damaging Het
Grm5 A G 7: 87,685,278 (GRCm39) Y465C probably damaging Het
Idh3b T A 2: 130,126,321 (GRCm39) N6I probably benign Het
Ighmbp2 T C 19: 3,323,022 (GRCm39) K308R possibly damaging Het
Lrch1 A T 14: 75,073,202 (GRCm39) S146T possibly damaging Het
Lyl1 C T 8: 85,429,300 (GRCm39) P3L possibly damaging Het
Mterf3 T C 13: 67,078,221 (GRCm39) K16R probably damaging Het
Ncapg T A 5: 45,853,010 (GRCm39) H825Q probably damaging Het
Or2t1 G A 14: 14,328,851 (GRCm38) V247I probably damaging Het
Or2y1f T A 11: 49,184,988 (GRCm39) I280N probably damaging Het
Or4d5 A G 9: 40,012,030 (GRCm39) V252A probably damaging Het
Or5b95 G A 19: 12,658,287 (GRCm39) V272M possibly damaging Het
Or5w15 A T 2: 87,568,462 (GRCm39) S69T probably benign Het
Pald1 A T 10: 61,182,884 (GRCm39) M355K probably benign Het
Phc1 A G 6: 122,300,428 (GRCm39) probably benign Het
Phkb T A 8: 86,745,095 (GRCm39) probably benign Het
Pkn3 G T 2: 29,975,257 (GRCm39) R506L probably damaging Het
Plod2 T C 9: 92,455,620 (GRCm39) Y100H probably damaging Het
Prl7b1 G T 13: 27,790,918 (GRCm39) Q56K probably benign Het
Rhot1 T A 11: 80,133,407 (GRCm39) C229* probably null Het
Sema3a G A 5: 13,649,456 (GRCm39) R735Q probably damaging Het
Slc18b1 A G 10: 23,702,557 (GRCm39) *460W probably null Het
Slco6c1 T A 1: 96,993,748 (GRCm39) probably benign Het
Slu7 T A 11: 43,333,457 (GRCm39) V359D possibly damaging Het
Suco T C 1: 161,662,049 (GRCm39) Y794C possibly damaging Het
Sult3a2 T C 10: 33,655,769 (GRCm39) N70S probably benign Het
Taar2 A T 10: 23,817,195 (GRCm39) D245V probably damaging Het
Taf1d A G 9: 15,221,237 (GRCm39) H181R possibly damaging Het
Tmem33 T C 5: 67,421,139 (GRCm39) S38P probably damaging Het
Traf3ip1 T C 1: 91,450,609 (GRCm39) S519P probably benign Het
Ttc12 T C 9: 49,369,362 (GRCm39) K253E possibly damaging Het
Other mutations in Or5t15
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02010:Or5t15 APN 2 86,681,541 (GRCm39) missense possibly damaging 0.77
IGL02947:Or5t15 APN 2 86,681,130 (GRCm39) missense probably benign 0.00
R0631:Or5t15 UTSW 2 86,681,311 (GRCm39) missense probably benign 0.07
R1640:Or5t15 UTSW 2 86,681,571 (GRCm39) missense probably benign 0.05
R1718:Or5t15 UTSW 2 86,681,531 (GRCm39) missense probably benign 0.22
R1936:Or5t15 UTSW 2 86,681,745 (GRCm39) missense probably benign 0.01
R3720:Or5t15 UTSW 2 86,681,935 (GRCm39) missense probably benign 0.16
R4177:Or5t15 UTSW 2 86,681,745 (GRCm39) missense possibly damaging 0.56
R5378:Or5t15 UTSW 2 86,681,807 (GRCm39) missense probably benign
R5589:Or5t15 UTSW 2 86,681,118 (GRCm39) missense unknown
R6158:Or5t15 UTSW 2 86,681,859 (GRCm39) missense possibly damaging 0.92
R6326:Or5t15 UTSW 2 86,681,338 (GRCm39) missense probably benign 0.00
R6637:Or5t15 UTSW 2 86,681,784 (GRCm39) missense probably benign 0.01
Z1176:Or5t15 UTSW 2 86,681,284 (GRCm39) missense
Posted On 2016-08-02