Incidental Mutation 'R2322:Or2y17'
ID 244784
Institutional Source Beutler Lab
Gene Symbol Or2y17
Ensembl Gene ENSMUSG00000045421
Gene Name olfactory receptor family 2 subfamily Y member 17
Synonyms GA_x6K02T2QP88-6094111-6093176, MOR256-2, Olfr1390
Accession Numbers
Essential gene? Probably non essential (E-score: 0.077) question?
Stock # R2322 (G1)
Quality Score 225
Status Not validated
Chromosome 11
Chromosomal Location 49231361-49232296 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 49231476 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Arginine at position 39 (L39R)
Ref Sequence ENSEMBL: ENSMUSP00000151059 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000062719] [ENSMUST00000215014]
AlphaFold Q8VGW9
Predicted Effect probably damaging
Transcript: ENSMUST00000062719
AA Change: L39R

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000053611
Gene: ENSMUSG00000045421
AA Change: L39R

DomainStartEndE-ValueType
Pfam:7tm_4 31 307 2.5e-45 PFAM
Pfam:7TM_GPCR_Srsx 35 230 2.8e-6 PFAM
Pfam:7tm_1 41 289 2.3e-24 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000215014
AA Change: L39R

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.5%
  • 20x: 95.7%
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
A2ml1 C T 6: 128,557,349 (GRCm39) A115T probably benign Het
AY358078 A G 14: 52,042,147 (GRCm39) Y174C unknown Het
Bod1l A T 5: 41,984,463 (GRCm39) V529E probably benign Het
Brinp3 A G 1: 146,577,492 (GRCm39) T176A probably benign Het
Ccn2 T C 10: 24,472,732 (GRCm39) M214T probably damaging Het
Cfap57 T A 4: 118,467,922 (GRCm39) I272L probably benign Het
Cnr1 A G 4: 33,944,514 (GRCm39) K301E probably damaging Het
Elavl1 A T 8: 4,339,802 (GRCm39) L260H probably damaging Het
Ercc6 A G 14: 32,248,274 (GRCm39) Y275C probably damaging Het
Fndc1 A G 17: 8,007,847 (GRCm39) S96P probably damaging Het
Hykk G A 9: 54,853,418 (GRCm39) G247S probably benign Het
Ky T C 9: 102,414,990 (GRCm39) probably null Het
Mcu A C 10: 59,290,766 (GRCm39) probably null Het
Or5w11 T C 2: 87,459,118 (GRCm39) C104R possibly damaging Het
Ppp4r3a C T 12: 101,008,878 (GRCm39) R667Q probably damaging Het
Ptprj T C 2: 90,301,473 (GRCm39) T220A probably benign Het
St18 T A 1: 6,914,348 (GRCm39) C766* probably null Het
St8sia4 C T 1: 95,581,463 (GRCm39) R93H probably damaging Het
Tcim G C 8: 24,928,726 (GRCm39) R63G probably damaging Het
Xylb T C 9: 119,217,813 (GRCm39) S488P possibly damaging Het
Zhx3 T C 2: 160,623,948 (GRCm39) D73G probably damaging Het
Other mutations in Or2y17
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02176:Or2y17 APN 11 49,232,133 (GRCm39) missense probably benign 0.44
IGL02334:Or2y17 APN 11 49,232,018 (GRCm39) missense probably benign 0.09
IGL02958:Or2y17 APN 11 49,232,127 (GRCm39) missense probably benign 0.44
PIT4402001:Or2y17 UTSW 11 49,232,226 (GRCm39) missense probably damaging 1.00
R0149:Or2y17 UTSW 11 49,231,641 (GRCm39) missense probably benign 0.07
R0361:Or2y17 UTSW 11 49,231,641 (GRCm39) missense probably benign 0.07
R0417:Or2y17 UTSW 11 49,231,500 (GRCm39) missense possibly damaging 0.88
R1187:Or2y17 UTSW 11 49,231,417 (GRCm39) missense probably damaging 1.00
R1859:Or2y17 UTSW 11 49,232,211 (GRCm39) missense probably damaging 1.00
R1882:Or2y17 UTSW 11 49,231,539 (GRCm39) missense probably damaging 1.00
R1885:Or2y17 UTSW 11 49,231,662 (GRCm39) missense probably damaging 1.00
R2193:Or2y17 UTSW 11 49,231,770 (GRCm39) missense possibly damaging 0.70
R3929:Or2y17 UTSW 11 49,231,820 (GRCm39) missense probably benign 0.00
R4739:Or2y17 UTSW 11 49,232,148 (GRCm39) missense probably benign 0.00
R4939:Or2y17 UTSW 11 49,231,376 (GRCm39) missense probably benign 0.00
R5977:Or2y17 UTSW 11 49,231,592 (GRCm39) missense probably damaging 0.96
R6338:Or2y17 UTSW 11 49,231,694 (GRCm39) missense probably benign 0.30
R6864:Or2y17 UTSW 11 49,231,580 (GRCm39) missense probably damaging 0.99
R7045:Or2y17 UTSW 11 49,231,757 (GRCm39) missense probably damaging 0.96
R7276:Or2y17 UTSW 11 49,231,821 (GRCm39) missense probably benign 0.33
R7339:Or2y17 UTSW 11 49,231,875 (GRCm39) missense not run
R8355:Or2y17 UTSW 11 49,231,592 (GRCm39) missense possibly damaging 0.89
R8497:Or2y17 UTSW 11 49,231,721 (GRCm39) missense probably damaging 1.00
R8715:Or2y17 UTSW 11 49,232,154 (GRCm39) missense probably damaging 1.00
R9587:Or2y17 UTSW 11 49,232,007 (GRCm39) missense probably benign 0.22
Predicted Primers PCR Primer
(F):5'- GACCAATGCTCTGTTCTGTGC -3'
(R):5'- TCTGTGGTGGCTAAAGCAAGG -3'

Sequencing Primer
(F):5'- AATGCTCTGTTCTGTGCTCTTCCTAG -3'
(R):5'- GAAGAGCTGGGCCACACAC -3'
Posted On 2014-10-30