Incidental Mutation 'R5543:Or2z2'
ID 436112
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 043101-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.075) question?
Stock # R5543 (G1)
Quality Score 225
Status Not validated
Chromosome 11
Chromosomal Location 58345741-58346806 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 58345993 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Leucine at position 261 (M261L)
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: M261L

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000055961
Gene: ENSMUSG00000043314
AA Change: M261L

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: M261L

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.2%
  • 20x: 94.7%
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: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9130023H24Rik C A 7: 127,836,353 (GRCm39) S80I probably benign Het
Aak1 T C 6: 86,959,627 (GRCm39) probably null Het
Abcc6 A G 7: 45,638,960 (GRCm39) probably null Het
Acvr1 A G 2: 58,353,157 (GRCm39) S268P probably damaging Het
Apod T C 16: 31,122,351 (GRCm39) probably null Het
Atp5po T C 16: 91,723,418 (GRCm39) I58V probably benign Het
AU040320 C T 4: 126,735,017 (GRCm39) T777M probably damaging Het
Ccne2 A T 4: 11,194,026 (GRCm39) N89I probably benign Het
Cspg4b C A 13: 113,457,407 (GRCm39) T1151K probably damaging Het
Dnah7a A G 1: 53,543,228 (GRCm39) V2314A probably damaging Het
Dop1b T C 16: 93,595,808 (GRCm39) S1881P probably damaging Het
E4f1 A G 17: 24,666,336 (GRCm39) V24A possibly damaging Het
Esrrg A T 1: 187,882,451 (GRCm39) D236V probably damaging Het
Fam240b T A 13: 64,633,736 (GRCm39) I27F possibly damaging Het
Fat1 T A 8: 45,476,516 (GRCm39) I1854N probably damaging Het
Fchsd2 T C 7: 100,920,906 (GRCm39) Y480H probably damaging Het
Fras1 A G 5: 96,676,394 (GRCm39) N47S probably benign Het
Gabrr3 T C 16: 59,253,870 (GRCm39) S196P probably damaging Het
Gbp8 T A 5: 105,165,696 (GRCm39) D319V possibly damaging Het
Hrh3 G T 2: 179,745,763 (GRCm39) A61E probably damaging Het
Idua T C 5: 108,818,095 (GRCm39) I89T probably benign Het
Ifitm3 T A 7: 140,589,730 (GRCm39) I108F unknown Het
Izumo4 T C 10: 80,538,668 (GRCm39) F40S probably damaging Het
Kifc2 A G 15: 76,551,242 (GRCm39) R679G probably damaging Het
Klk14 G A 7: 43,341,501 (GRCm39) C51Y probably damaging Het
Ldha A T 7: 46,500,314 (GRCm39) I171F possibly damaging Het
Lrfn4 T C 19: 4,662,191 (GRCm39) S609G probably benign Het
Mmp15 T C 8: 96,094,729 (GRCm39) F201S possibly damaging Het
Myof C T 19: 37,969,778 (GRCm39) V295I probably benign Het
Or1n2 C T 2: 36,797,369 (GRCm39) T137I possibly damaging Het
Or5m12 G T 2: 85,734,672 (GRCm39) A242D probably damaging Het
Parp14 T C 16: 35,655,137 (GRCm39) D1778G probably benign Het
Pcnt A T 10: 76,247,886 (GRCm39) D969E probably benign Het
Pibf1 A T 14: 99,350,428 (GRCm39) N192I probably benign Het
Pitpnm3 A G 11: 71,947,023 (GRCm39) F792S probably damaging Het
Pkd2 T A 5: 104,637,199 (GRCm39) I604N probably damaging Het
Pla2g15 T C 8: 106,887,775 (GRCm39) Y188H probably damaging Het
Plxnc1 G T 10: 94,700,636 (GRCm39) D643E probably benign Het
Prrc2c G A 1: 162,501,080 (GRCm39) P1241L probably damaging Het
Ptprd T C 4: 75,977,990 (GRCm39) E173G probably damaging Het
Shank3 T C 15: 89,416,557 (GRCm39) V232A probably damaging Het
Shbg A G 11: 69,507,564 (GRCm39) I171T probably damaging Het
Slc22a14 A T 9: 119,002,674 (GRCm39) F404L probably benign Het
Slc37a3 C A 6: 39,331,960 (GRCm39) G158C probably damaging Het
Slfn9 C A 11: 82,873,207 (GRCm39) L565F probably damaging Het
Spmip10 G A 18: 56,727,760 (GRCm39) probably benign Het
Trank1 T A 9: 111,195,180 (GRCm39) M1068K probably damaging Het
Trbv15 A T 6: 41,118,187 (GRCm39) I15L probably benign Het
Ttn C T 2: 76,569,918 (GRCm39) V26992M probably damaging Het
Ttn A T 2: 76,641,587 (GRCm39) L5176Q possibly damaging Het
Ugt2b34 T A 5: 87,054,560 (GRCm39) I74F probably damaging Het
Vamp3 A G 4: 151,135,477 (GRCm39) L47P probably damaging Het
Zfp143 T A 7: 109,682,522 (GRCm39) C363* probably null Het
Zfp438 T C 18: 5,213,761 (GRCm39) E399G probably damaging 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
R5433:Or2z2 UTSW 11 58,346,680 (GRCm39) missense probably damaging 0.99
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'- TGAGAGCTGAGGTACCCATC -3'
(R):5'- AAGCAGGTACTATTTGTGACGG -3'

Sequencing Primer
(F):5'- AGAGCTGAGGTACCCATCTCTCAG -3'
(R):5'- CAGGTACTATTTGTGACGGGTGTG -3'
Posted On 2016-10-24