Incidental Mutation 'IGL00937:Or2ag15'
ID 27836
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 # IGL00937
Quality Score
Status
Chromosome 7
Chromosomal Location 106340112-106341163 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 106340364 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Phenylalanine at position 259 (Y259F)
Ref Sequence ENSEMBL: ENSMUSP00000152039 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000050541] [ENSMUST00000217734]
AlphaFold Q8VFM4
Predicted Effect probably damaging
Transcript: ENSMUST00000050541
AA Change: Y259F

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000055207
Gene: ENSMUSG00000051591
AA Change: Y259F

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 damaging
Transcript: ENSMUST00000217734
AA Change: Y259F

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: 21 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Cc2d2a A T 5: 43,845,464 (GRCm39) probably null Het
Cd34 A G 1: 194,642,422 (GRCm39) E381G probably damaging Het
Chka A G 19: 3,942,189 (GRCm39) E381G probably benign Het
Dennd1b T A 1: 139,097,977 (GRCm39) C673S probably benign Het
E130308A19Rik G A 4: 59,690,846 (GRCm39) A227T probably benign Het
F13b T A 1: 139,445,098 (GRCm39) probably benign Het
Hipk3 T C 2: 104,263,517 (GRCm39) N933D possibly damaging Het
Mmp27 T C 9: 7,578,900 (GRCm39) probably benign Het
Nod1 C T 6: 54,914,349 (GRCm39) V815I probably benign Het
Or2a5 T A 6: 42,873,568 (GRCm39) F61Y probably damaging Het
Or3a1d C T 11: 74,238,255 (GRCm39) V52I probably benign Het
Or51ab3 C A 7: 103,201,064 (GRCm39) A24E probably damaging Het
Or51h1 T A 7: 102,308,555 (GRCm39) S176T probably damaging Het
Or52k2 T A 7: 102,253,564 (GRCm39) M1K probably null Het
Pms1 T A 1: 53,314,410 (GRCm39) E45V possibly damaging Het
Prkcsh T C 9: 21,917,861 (GRCm39) S126P possibly damaging Het
Pros1 A T 16: 62,730,408 (GRCm39) L299F probably damaging Het
Scrn1 A G 6: 54,497,718 (GRCm39) I291T probably benign Het
Slc15a2 A T 16: 36,572,242 (GRCm39) Y676* probably null Het
Tenm2 A C 11: 35,915,450 (GRCm39) V2028G probably damaging Het
Trpa1 T C 1: 14,950,501 (GRCm39) probably benign Het
Other mutations in Or2ag15
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00226:Or2ag15 APN 7 106,340,908 (GRCm39) missense probably benign 0.20
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
IGL02654:Or2ag15 APN 7 106,340,555 (GRCm39) nonsense probably null
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 2013-04-17