Incidental Mutation 'R5433:Or2z2'
ID 428168
Institutional Source Beutler Lab
Gene Symbol Or2z2
Ensembl Gene ENSMUSG00000043314
Gene Name olfactory receptor family 2 subfamily Z member 2
Synonyms MOR281-1, MTPCR07, GA_x6K02T2NKPP-957001-957948, Olfr30
MMRRC Submission 042998-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.083) question?
Stock # R5433 (G1)
Quality Score 225
Status Validated
Chromosome 11
Chromosomal Location 58345741-58346806 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 58346680 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Methionine at position 32 (V32M)
Ref Sequence ENSEMBL: ENSMUSP00000148907 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055204] [ENSMUST00000064614] [ENSMUST00000215691]
AlphaFold Q8VGD8
Predicted Effect probably damaging
Transcript: ENSMUST00000055204
AA Change: V32M

PolyPhen 2 Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000055961
Gene: ENSMUSG00000043314
AA Change: V32M

DomainStartEndE-ValueType
Pfam:7tm_4 32 308 1.9e-53 PFAM
Pfam:7TM_GPCR_Srsx 36 252 1.7e-6 PFAM
Pfam:7tm_1 42 291 8.3e-25 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000064614
SMART Domains Protein: ENSMUSP00000063665
Gene: ENSMUSG00000052642

DomainStartEndE-ValueType
signal peptide 1 24 N/A INTRINSIC
Pfam:UPAR_LY6 47 124 1.3e-6 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000215691
AA Change: V32M

PolyPhen 2 Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.8%
Validation Efficiency 100% (58/58)
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: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700019D03Rik T C 1: 52,964,657 (GRCm39) S24G probably damaging Het
1810064F22Rik A G 9: 22,119,039 (GRCm39) noncoding transcript Het
Aacs A T 5: 125,592,078 (GRCm39) M589L probably benign Het
Adamts8 A C 9: 30,873,012 (GRCm39) H739P probably benign Het
Atp8b2 T C 3: 89,860,216 (GRCm39) probably benign Het
BC030500 A G 8: 59,366,043 (GRCm39) probably benign Het
Btnl9 T A 11: 49,066,830 (GRCm39) probably benign Het
Cd74 G T 18: 60,940,993 (GRCm39) A31S probably benign Het
Ceacam3 G A 7: 16,893,808 (GRCm39) A440T possibly damaging Het
Ces1d G A 8: 93,912,664 (GRCm39) T258I probably benign Het
Col10a1 A G 10: 34,266,735 (GRCm39) probably benign Het
Coro1b C T 19: 4,203,449 (GRCm39) A430V probably benign Het
Cyp2c65 A T 19: 39,081,928 (GRCm39) I485L probably benign Het
Dio1 A T 4: 107,163,977 (GRCm39) probably benign Het
Dmxl1 G A 18: 50,000,966 (GRCm39) probably null Het
Dynlt5 A G 4: 102,859,700 (GRCm39) E84G possibly damaging Het
Elp6 A G 9: 110,144,851 (GRCm39) Y136C probably damaging Het
Gon4l A T 3: 88,803,532 (GRCm39) Q1382L possibly damaging Het
Guca1a T C 17: 47,711,295 (GRCm39) E17G probably damaging Het
Gucy2d G A 7: 98,098,982 (GRCm39) G267E probably damaging Het
Gvin3 T A 7: 106,199,314 (GRCm39) noncoding transcript Het
Hspg2 T A 4: 137,256,105 (GRCm39) probably null Het
Il1a G T 2: 129,149,821 (GRCm39) D26E possibly damaging Het
Il22b T A 10: 118,130,789 (GRCm39) I36F probably damaging Het
Kcna1 A T 6: 126,620,075 (GRCm39) F82I probably damaging Het
Klhl18 G C 9: 110,265,195 (GRCm39) N335K possibly damaging Het
Lamtor5 T G 3: 107,189,323 (GRCm39) C120G probably benign Het
Lars1 A G 18: 42,384,363 (GRCm39) C72R possibly damaging Het
Lrrfip1 T G 1: 91,014,848 (GRCm39) probably null Het
Mapkapk3 T C 9: 107,133,491 (GRCm39) D349G probably damaging Het
Mknk2 A T 10: 80,503,059 (GRCm39) I421N probably benign Het
Myh6 A G 14: 55,191,381 (GRCm39) I820T probably benign Het
Notch2 T G 3: 98,033,450 (GRCm39) V1182G probably damaging Het
Or1af1 T G 2: 37,109,684 (GRCm39) F61C probably damaging Het
Or1e16 AGCGGTCGTAGGC AGC 11: 73,286,480 (GRCm39) probably null Het
Ppfia4 A T 1: 134,245,632 (GRCm39) S641T probably damaging Het
Prok1 T A 3: 107,146,949 (GRCm39) H6L probably benign Het
Ptprm A T 17: 67,000,468 (GRCm39) V1172E probably damaging Het
Rasal3 C T 17: 32,612,575 (GRCm39) R762Q probably benign Het
Rgs20 G T 1: 5,140,333 (GRCm39) A23E possibly damaging Het
Rprd1a T C 18: 24,640,288 (GRCm39) T163A probably benign Het
Rrm1 A T 7: 102,114,974 (GRCm39) N37I probably damaging Het
Shc4 T A 2: 125,481,350 (GRCm39) E520V probably damaging Het
Slc14a2 G T 18: 78,252,143 (GRCm39) P56Q probably damaging Het
Slc22a3 C T 17: 12,677,377 (GRCm39) G264S probably damaging Het
Svil A G 18: 5,059,294 (GRCm39) E770G probably damaging Het
Svop A G 5: 114,198,186 (GRCm39) V129A probably damaging Het
Szt2 A T 4: 118,232,663 (GRCm39) probably benign Het
Tcof1 T C 18: 60,951,105 (GRCm39) probably benign Het
Tmem30a T A 9: 79,687,930 (GRCm39) I80F probably damaging Het
Vmn2r16 G T 5: 109,511,708 (GRCm39) L638F probably damaging Het
Xkr7 T A 2: 152,896,244 (GRCm39) I366N probably damaging Het
Zer1 A G 2: 29,990,998 (GRCm39) probably benign Het
Other mutations in Or2z2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01305:Or2z2 APN 11 58,346,088 (GRCm39) missense probably damaging 1.00
IGL02001:Or2z2 APN 11 58,346,335 (GRCm39) missense probably benign 0.33
IGL02170:Or2z2 APN 11 58,345,906 (GRCm39) missense probably damaging 1.00
IGL02638:Or2z2 APN 11 58,345,873 (GRCm39) missense probably damaging 1.00
ANU22:Or2z2 UTSW 11 58,346,088 (GRCm39) missense probably damaging 1.00
R0502:Or2z2 UTSW 11 58,346,140 (GRCm39) missense possibly damaging 0.54
R0784:Or2z2 UTSW 11 58,346,131 (GRCm39) missense possibly damaging 0.63
R1300:Or2z2 UTSW 11 58,346,667 (GRCm39) missense probably damaging 1.00
R1451:Or2z2 UTSW 11 58,346,358 (GRCm39) missense probably benign 0.00
R1642:Or2z2 UTSW 11 58,346,664 (GRCm39) missense probably benign
R1754:Or2z2 UTSW 11 58,346,088 (GRCm39) missense probably damaging 1.00
R1854:Or2z2 UTSW 11 58,346,257 (GRCm39) missense probably damaging 1.00
R2920:Or2z2 UTSW 11 58,346,403 (GRCm39) missense probably damaging 1.00
R3160:Or2z2 UTSW 11 58,346,053 (GRCm39) missense probably damaging 1.00
R3162:Or2z2 UTSW 11 58,346,053 (GRCm39) missense probably damaging 1.00
R4791:Or2z2 UTSW 11 58,346,370 (GRCm39) missense possibly damaging 0.83
R4964:Or2z2 UTSW 11 58,346,733 (GRCm39) missense probably benign 0.05
R5543:Or2z2 UTSW 11 58,345,993 (GRCm39) missense probably damaging 1.00
R6649:Or2z2 UTSW 11 58,346,394 (GRCm39) missense probably damaging 0.98
R6653:Or2z2 UTSW 11 58,346,394 (GRCm39) missense probably damaging 0.98
R7388:Or2z2 UTSW 11 58,346,481 (GRCm39) missense probably damaging 1.00
R7492:Or2z2 UTSW 11 58,346,715 (GRCm39) missense probably benign 0.28
R7566:Or2z2 UTSW 11 58,346,489 (GRCm39) missense probably benign 0.02
R7567:Or2z2 UTSW 11 58,345,992 (GRCm39) missense probably damaging 1.00
R8557:Or2z2 UTSW 11 58,346,562 (GRCm39) missense probably damaging 1.00
R8777:Or2z2 UTSW 11 58,346,757 (GRCm39) nonsense probably null
R8777-TAIL:Or2z2 UTSW 11 58,346,757 (GRCm39) nonsense probably null
R8810:Or2z2 UTSW 11 58,345,936 (GRCm39) missense possibly damaging 0.54
R9139:Or2z2 UTSW 11 58,345,999 (GRCm39) missense possibly damaging 0.92
Z1177:Or2z2 UTSW 11 58,346,363 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TCCGAAAGAGATGCTCGTCC -3'
(R):5'- TGGTTTTCCTGTGAAATAATGACCC -3'

Sequencing Primer
(F):5'- GAGATGCTCGTCCAACCAAAGAG -3'
(R):5'- TGACCCTACAAATACTGGCTAGGTG -3'
Posted On 2016-09-01