Incidental Mutation 'R1451:Or2w2'
ID 161689
Institutional Source Beutler Lab
Gene Symbol Or2w2
Ensembl Gene ENSMUSG00000046016
Gene Name olfactory receptor family 2 subfamily W member 2
Synonyms GA_x6K02T2QHY8-11663090-11664010, MOR256-13, Olfr1364
MMRRC Submission 039506-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.099) question?
Stock # R1451 (G1)
Quality Score 225
Status Validated
Chromosome 13
Chromosomal Location 21757680-21758624 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 21758457 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 56 (Y56*)
Ref Sequence ENSEMBL: ENSMUSP00000149964 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000057453] [ENSMUST00000206526] [ENSMUST00000213912]
AlphaFold Q5SZS9
Predicted Effect probably null
Transcript: ENSMUST00000057453
AA Change: Y56*
SMART Domains Protein: ENSMUSP00000059544
Gene: ENSMUSG00000046016
AA Change: Y56*

DomainStartEndE-ValueType
Pfam:7tm_4 36 314 1.2e-48 PFAM
Pfam:7tm_1 47 296 3.9e-24 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000206526
AA Change: Y56*
Predicted Effect probably null
Transcript: ENSMUST00000213912
AA Change: Y56*
Predicted Effect noncoding transcript
Transcript: ENSMUST00000216898
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 98.8%
  • 3x: 97.8%
  • 10x: 94.4%
  • 20x: 86.3%
Validation Efficiency 96% (55/57)
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: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700024G13Rik T C 14: 32,098,588 (GRCm39) E83G possibly damaging Het
Abca9 A G 11: 110,018,273 (GRCm39) S1116P probably damaging Het
Abcc12 T A 8: 87,284,322 (GRCm39) T296S probably damaging Het
Adarb2 A G 13: 8,389,657 (GRCm39) probably benign Het
Arhgef12 C T 9: 42,903,874 (GRCm39) probably benign Het
Asah1 A G 8: 41,807,049 (GRCm39) probably null Het
C1ra A T 6: 124,498,600 (GRCm39) Q431L probably benign Het
C1s2 A T 6: 124,602,453 (GRCm39) I580N probably benign Het
Cacna2d4 C T 6: 119,213,785 (GRCm39) T68I probably benign Het
Car8 A T 4: 8,189,327 (GRCm39) H162Q probably benign Het
Ccdc106 A G 7: 5,062,527 (GRCm39) R116G probably damaging Het
Ccdc136 T A 6: 29,419,376 (GRCm39) N965K probably benign Het
Cd200r3 A G 16: 44,771,910 (GRCm39) E58G possibly damaging Het
Cnksr3 T A 10: 7,076,830 (GRCm39) S121C probably null Het
Cog6 T C 3: 52,916,534 (GRCm39) M212V possibly damaging Het
Ebna1bp2 C A 4: 118,478,269 (GRCm39) probably null Het
Epha1 C A 6: 42,338,385 (GRCm39) M730I probably damaging Het
Fcgbpl1 T C 7: 27,836,582 (GRCm39) F167S probably damaging Het
Fscn2 A T 11: 120,252,848 (GRCm39) E105V probably damaging Het
Gars1 T C 6: 55,030,108 (GRCm39) probably benign Het
Itgb4 G T 11: 115,881,710 (GRCm39) G753V probably damaging Het
Kif23 C T 9: 61,832,084 (GRCm39) V634M probably damaging Het
Krt8 T C 15: 101,907,264 (GRCm39) Y273C possibly damaging Het
Lgmn A G 12: 102,372,151 (GRCm39) probably benign Het
Lrig3 T C 10: 125,845,926 (GRCm39) I785T possibly damaging Het
Lrriq1 A G 10: 103,038,376 (GRCm39) probably benign Het
Lta4h A G 10: 93,316,590 (GRCm39) D491G probably damaging Het
Megf10 A T 18: 57,385,931 (GRCm39) S315C probably damaging Het
Mphosph8 C T 14: 56,905,878 (GRCm39) R24C possibly damaging Het
Neurog2 A G 3: 127,427,490 (GRCm39) D38G possibly damaging Het
Or1j11 G T 2: 36,311,877 (GRCm39) A156S probably benign Het
Or2z2 C T 11: 58,346,358 (GRCm39) R139H probably benign Het
Or6b3 T A 1: 92,439,517 (GRCm39) I78F possibly damaging Het
Or8b50 A T 9: 38,518,234 (GRCm39) I158F probably benign Het
Or8g50 T A 9: 39,648,612 (GRCm39) V167D probably benign Het
Pcdhb17 A T 18: 37,619,989 (GRCm39) D593V probably damaging Het
Pde2a G T 7: 101,071,198 (GRCm39) E23* probably null Het
Prex2 G A 1: 11,226,483 (GRCm39) V749I probably benign Het
Ptchd4 A G 17: 42,813,809 (GRCm39) Y570C probably damaging Het
Robo3 C T 9: 37,329,007 (GRCm39) R1237K probably benign Het
Slc6a1 C A 6: 114,284,756 (GRCm39) Y87* probably null Het
Snx13 G A 12: 35,128,983 (GRCm39) A34T probably benign Het
Sppl3 T C 5: 115,226,424 (GRCm39) L193P probably damaging Het
Tia1 A T 6: 86,407,321 (GRCm39) Y277F probably benign Het
Tns2 C T 15: 102,017,369 (GRCm39) R281C probably damaging Het
Trappc2l T C 8: 123,342,134 (GRCm39) F127L probably damaging Het
Ushbp1 G T 8: 71,838,663 (GRCm39) Q588K possibly damaging Het
Usp43 T A 11: 67,747,007 (GRCm39) H895L probably benign Het
Vmn1r179 T A 7: 23,628,275 (GRCm39) C155* probably null Het
Vmn2r8 T A 5: 108,945,933 (GRCm39) D558V probably damaging Het
Vps13a T C 19: 16,688,228 (GRCm39) T860A probably benign Het
Vps50 A G 6: 3,565,628 (GRCm39) N522S possibly damaging Het
Zfp180 T C 7: 23,804,643 (GRCm39) F354S probably benign Het
Zgpat A G 2: 181,021,984 (GRCm39) probably benign Het
Other mutations in Or2w2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01485:Or2w2 APN 13 21,758,627 (GRCm39) splice site probably null
IGL01925:Or2w2 APN 13 21,758,341 (GRCm39) missense possibly damaging 0.70
R0540:Or2w2 UTSW 13 21,757,948 (GRCm39) missense probably benign 0.01
R1268:Or2w2 UTSW 13 21,758,498 (GRCm39) missense probably benign 0.15
R1572:Or2w2 UTSW 13 21,758,480 (GRCm39) missense possibly damaging 0.53
R1781:Or2w2 UTSW 13 21,757,711 (GRCm39) missense probably damaging 0.98
R1927:Or2w2 UTSW 13 21,758,426 (GRCm39) missense probably benign 0.11
R4611:Or2w2 UTSW 13 21,757,744 (GRCm39) missense probably damaging 0.98
R4750:Or2w2 UTSW 13 21,757,913 (GRCm39) missense possibly damaging 0.48
R5493:Or2w2 UTSW 13 21,758,042 (GRCm39) missense probably damaging 1.00
R7192:Or2w2 UTSW 13 21,758,539 (GRCm39) missense probably damaging 1.00
R7611:Or2w2 UTSW 13 21,758,488 (GRCm39) missense probably benign 0.06
R8017:Or2w2 UTSW 13 21,758,648 (GRCm39) start gained probably benign
R8819:Or2w2 UTSW 13 21,757,999 (GRCm39) missense probably benign 0.44
R8965:Or2w2 UTSW 13 21,758,387 (GRCm39) missense probably benign 0.30
R8974:Or2w2 UTSW 13 21,758,203 (GRCm39) missense probably damaging 0.98
R8978:Or2w2 UTSW 13 21,758,279 (GRCm39) missense probably benign 0.44
Predicted Primers PCR Primer
(F):5'- TCACCTGACATCTGCCACATCGAG -3'
(R):5'- ATGCCATGATCAACCAGAGCTGCC -3'

Sequencing Primer
(F):5'- AGGCAGCTTCATGGTCACAG -3'
(R):5'- GCTGCCAGGAACAGTTCATC -3'
Posted On 2014-03-14