Incidental Mutation 'IGL02654:Or2ag15'
ID 302269
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or2ag15
Ensembl Gene ENSMUSG00000051591
Gene Name olfactory receptor family 2 subfamily AG member 15
Synonyms GA_x6K02T2PBJ9-9119301-9118348, Olfr697, MOR283-5
Accession Numbers
Essential gene? Probably non essential (E-score: 0.080) question?
Stock # IGL02654
Quality Score
Status
Chromosome 7
Chromosomal Location 106340112-106341163 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 106340555 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 195 (Y195*)
Ref Sequence ENSEMBL: ENSMUSP00000152039 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000050541] [ENSMUST00000217734]
AlphaFold Q8VFM4
Predicted Effect probably null
Transcript: ENSMUST00000050541
AA Change: Y195*
SMART Domains Protein: ENSMUSP00000055207
Gene: ENSMUSG00000051591
AA Change: Y195*

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 1.2e-46 PFAM
Pfam:7TM_GPCR_Srsx 35 305 4.7e-7 PFAM
Pfam:7tm_1 41 290 8.7e-26 PFAM
Pfam:7TM_GPCR_Srx 69 306 4.3e-6 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000217734
AA Change: Y195*
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: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb4 T C 5: 8,977,826 (GRCm39) I468T possibly damaging Het
Actmap A G 7: 26,903,298 (GRCm39) E289G probably damaging Het
Anxa13 A G 15: 58,205,397 (GRCm39) noncoding transcript Het
Arhgef33 A G 17: 80,677,740 (GRCm39) Y429C probably damaging Het
Bdh1 T C 16: 31,275,433 (GRCm39) probably benign Het
Dennd4a A G 9: 64,817,473 (GRCm39) probably benign Het
Dld G T 12: 31,383,916 (GRCm39) H396N probably benign Het
Dsg1b T C 18: 20,542,319 (GRCm39) V942A probably damaging Het
Eln A T 5: 134,745,908 (GRCm39) probably benign Het
Fat3 G A 9: 15,908,271 (GRCm39) T2577M possibly damaging Het
Gad1 A T 2: 70,403,125 (GRCm39) K73M possibly damaging Het
Gipc1 T C 8: 84,389,780 (GRCm39) V253A probably damaging Het
Gtpbp10 A C 5: 5,593,372 (GRCm39) probably benign Het
Hgf A T 5: 16,766,049 (GRCm39) T62S probably benign Het
Hivep1 T C 13: 42,311,161 (GRCm39) S1134P probably damaging Het
Hnrnpc A G 14: 52,321,574 (GRCm39) L80S probably damaging Het
Kif20a G A 18: 34,765,076 (GRCm39) R770H probably damaging Het
Lcat T C 8: 106,666,401 (GRCm39) T374A possibly damaging Het
Mlana A G 19: 29,682,018 (GRCm39) probably null Het
Nhsl3 C T 4: 129,116,112 (GRCm39) G851R probably damaging Het
Nynrin A G 14: 56,100,716 (GRCm39) I169V possibly damaging Het
P3h3 A G 6: 124,822,228 (GRCm39) V585A possibly damaging Het
Pcdhb17 T A 18: 37,619,614 (GRCm39) M468K probably benign Het
Prl8a2 T G 13: 27,536,780 (GRCm39) I134S possibly damaging Het
Rev3l T C 10: 39,738,730 (GRCm39) V2828A probably damaging Het
Rhbdd1 G T 1: 82,320,504 (GRCm39) V163F probably benign Het
Rrp1 A G 10: 78,248,773 (GRCm39) V5A probably benign Het
Sephs1 A T 2: 4,889,366 (GRCm39) N48I probably benign Het
Speer4a3 T A 5: 26,158,205 (GRCm39) H49L probably benign Het
Vmn1r71 A G 7: 10,482,242 (GRCm39) Y149H probably benign Het
Wiz T C 17: 32,578,324 (GRCm39) D396G probably damaging Het
Xirp2 A G 2: 67,345,015 (GRCm39) S2419G possibly damaging Het
Zfp128 A G 7: 12,618,606 (GRCm39) T35A possibly damaging Het
Zmym2 T A 14: 57,148,772 (GRCm39) F362Y probably damaging Het
Other mutations in Or2ag15
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00226:Or2ag15 APN 7 106,340,908 (GRCm39) missense probably benign 0.20
IGL00937:Or2ag15 APN 7 106,340,364 (GRCm39) missense probably damaging 1.00
IGL01368:Or2ag15 APN 7 106,340,829 (GRCm39) missense probably benign 0.19
IGL01410:Or2ag15 APN 7 106,340,706 (GRCm39) missense probably benign 0.19
IGL01415:Or2ag15 APN 7 106,340,706 (GRCm39) missense probably benign 0.19
IGL01962:Or2ag15 APN 7 106,340,991 (GRCm39) missense probably benign 0.12
IGL02903:Or2ag15 APN 7 106,340,917 (GRCm39) missense probably damaging 1.00
IGL03347:Or2ag15 APN 7 106,340,177 (GRCm39) utr 3 prime probably benign
IGL03391:Or2ag15 APN 7 106,340,962 (GRCm39) missense probably damaging 1.00
R0139:Or2ag15 UTSW 7 106,340,832 (GRCm39) missense probably benign 0.05
R0142:Or2ag15 UTSW 7 106,340,972 (GRCm39) missense probably benign 0.36
R1293:Or2ag15 UTSW 7 106,341,058 (GRCm39) missense probably damaging 0.98
R1522:Or2ag15 UTSW 7 106,340,212 (GRCm39) missense probably benign 0.03
R1715:Or2ag15 UTSW 7 106,340,755 (GRCm39) missense probably damaging 1.00
R1959:Or2ag15 UTSW 7 106,340,601 (GRCm39) missense probably damaging 1.00
R1960:Or2ag15 UTSW 7 106,340,601 (GRCm39) missense probably damaging 1.00
R2031:Or2ag15 UTSW 7 106,341,105 (GRCm39) missense probably damaging 1.00
R4790:Or2ag15 UTSW 7 106,340,998 (GRCm39) missense probably benign 0.05
R5550:Or2ag15 UTSW 7 106,340,340 (GRCm39) missense probably benign 0.01
R6232:Or2ag15 UTSW 7 106,340,761 (GRCm39) missense probably damaging 0.96
R6293:Or2ag15 UTSW 7 106,340,613 (GRCm39) missense probably damaging 1.00
R6643:Or2ag15 UTSW 7 106,340,911 (GRCm39) missense probably benign 0.06
R7831:Or2ag15 UTSW 7 106,340,620 (GRCm39) missense probably damaging 0.99
R8013:Or2ag15 UTSW 7 106,340,824 (GRCm39) missense probably benign 0.00
R8014:Or2ag15 UTSW 7 106,340,824 (GRCm39) missense probably benign 0.00
R8883:Or2ag15 UTSW 7 106,340,274 (GRCm39) missense possibly damaging 0.74
R9072:Or2ag15 UTSW 7 106,340,759 (GRCm39) nonsense probably null
RF018:Or2ag15 UTSW 7 106,340,692 (GRCm39) missense probably benign 0.02
X0020:Or2ag15 UTSW 7 106,340,343 (GRCm39) missense probably damaging 0.97
Z1088:Or2ag15 UTSW 7 106,340,350 (GRCm39) missense probably benign 0.21
Posted On 2015-04-16