Incidental Mutation 'R6858:Or6c213'
ID 535379
Institutional Source Beutler Lab
Gene Symbol Or6c213
Ensembl Gene ENSMUSG00000071065
Gene Name olfactory receptor family 6 subfamily C member 213
Synonyms MOR110-5, GA_x6K02T2PULF-11417610-11416669, Olfr806, MOR110-12
MMRRC Submission 044960-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.050) question?
Stock # R6858 (G1)
Quality Score 225.009
Status Validated
Chromosome 10
Chromosomal Location 129573843-129574784 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 129574333 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Serine at position 151 (F151S)
Ref Sequence ENSEMBL: ENSMUSP00000150380 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000095245] [ENSMUST00000213239] [ENSMUST00000215142]
AlphaFold Q8VFI2
Predicted Effect probably damaging
Transcript: ENSMUST00000095245
AA Change: F151S

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000092873
Gene: ENSMUSG00000071065
AA Change: F151S

DomainStartEndE-ValueType
Pfam:7tm_4 28 306 2.6e-52 PFAM
Pfam:7tm_1 39 288 4.5e-22 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000213239
AA Change: F151S

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
Predicted Effect probably damaging
Transcript: ENSMUST00000215142
AA Change: F151S

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
Meta Mutation Damage Score 0.6329 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.5%
  • 20x: 98.4%
Validation Efficiency 96% (49/51)
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: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aldob T C 4: 49,538,796 (GRCm39) T241A probably benign Het
Arid4a A G 12: 71,070,283 (GRCm39) I65V probably benign Het
Bhmt2 C T 13: 93,807,948 (GRCm39) E47K probably damaging Het
Bpifa3 G A 2: 153,979,514 (GRCm39) G213D probably benign Het
C4b C G 17: 34,948,805 (GRCm39) A1548P probably damaging Het
Ccdc39 A G 3: 33,874,017 (GRCm39) V605A probably damaging Het
Cept1 A T 3: 106,420,195 (GRCm39) probably null Het
Cntrl T C 2: 35,052,107 (GRCm39) probably null Het
Col3a1 A G 1: 45,385,144 (GRCm39) D87G probably damaging Het
Crim1 A T 17: 78,623,056 (GRCm39) E418V probably damaging Het
Crtac1 T C 19: 42,307,174 (GRCm39) I196M possibly damaging Het
Crtap T C 9: 114,209,084 (GRCm39) Y320C probably damaging Het
Cttnbp2 A G 6: 18,448,452 (GRCm39) V27A probably damaging Het
Cyp2c69 G A 19: 39,866,009 (GRCm39) L195F probably benign Het
Cyp2d26 G A 15: 82,678,284 (GRCm39) R31C probably damaging Het
Fan1 T A 7: 64,022,234 (GRCm39) N340Y probably damaging Het
Fign G T 2: 63,810,157 (GRCm39) T371K probably benign Het
Fryl T C 5: 73,222,375 (GRCm39) T2069A probably damaging Het
Gm3486 A G 14: 41,210,322 (GRCm39) I53T probably damaging Het
Gprc5d T C 6: 135,093,313 (GRCm39) N198S possibly damaging Het
Ighv1-42 A G 12: 114,900,966 (GRCm39) S40P probably damaging Het
Itga8 A G 2: 12,204,892 (GRCm39) V515A probably benign Het
Kidins220 A T 12: 25,058,542 (GRCm39) I523L possibly damaging Het
Lmx1a A T 1: 167,660,450 (GRCm39) N245I probably damaging Het
Med22 T C 2: 26,795,949 (GRCm39) D157G possibly damaging Het
Ola1 T C 2: 72,927,574 (GRCm39) H335R probably damaging Het
Or1a1 A T 11: 74,086,925 (GRCm39) M199L probably benign Het
Or4c12 A G 2: 89,774,087 (GRCm39) I124T probably damaging Het
Or7e166 T C 9: 19,624,765 (GRCm39) I214T probably damaging Het
Or8h9 A G 2: 86,789,034 (GRCm39) I256T probably benign Het
Pde1a T A 2: 79,959,502 (GRCm39) probably benign Het
Pdgfrb G A 18: 61,198,219 (GRCm39) G304D probably benign Het
Potegl T C 2: 23,102,676 (GRCm39) V138A possibly damaging Het
Prune2 T A 19: 17,095,470 (GRCm39) C325S possibly damaging Het
Ptk2b T C 14: 66,450,847 (GRCm39) I40V probably damaging Het
Qrich1 A G 9: 108,411,333 (GRCm39) D286G probably damaging Het
Scn5a T C 9: 119,321,156 (GRCm39) I1469V probably benign Het
Serpina3k G A 12: 104,311,504 (GRCm39) A361T possibly damaging Het
Slc25a23 A G 17: 57,365,171 (GRCm39) Y73H probably damaging Het
Tmco3 A G 8: 13,363,924 (GRCm39) D82G probably damaging Het
Trbv28 G T 6: 41,248,624 (GRCm39) M51I probably damaging Het
Unc13b A T 4: 43,165,828 (GRCm39) H204L possibly damaging Het
Vamp5 G A 6: 72,357,424 (GRCm39) probably benign Het
Vmn1r25 T C 6: 57,955,996 (GRCm39) S98G probably benign Het
Vmn2r2 A G 3: 64,044,915 (GRCm39) F77S probably damaging Het
Vmn2r79 A T 7: 86,686,580 (GRCm39) M654L probably benign Het
Zfp985 A T 4: 147,667,764 (GRCm39) K211* probably null Het
Zwilch C T 9: 64,060,869 (GRCm39) D328N probably damaging Het
Other mutations in Or6c213
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01875:Or6c213 APN 10 129,574,791 (GRCm39) utr 5 prime probably benign
IGL02090:Or6c213 APN 10 129,574,181 (GRCm39) missense probably benign
IGL02328:Or6c213 APN 10 129,573,895 (GRCm39) missense probably benign 0.35
IGL02572:Or6c213 APN 10 129,574,735 (GRCm39) missense possibly damaging 0.81
R1773:Or6c213 UTSW 10 129,574,312 (GRCm39) missense probably damaging 0.97
R1797:Or6c213 UTSW 10 129,574,578 (GRCm39) missense probably benign 0.03
R4430:Or6c213 UTSW 10 129,574,130 (GRCm39) missense probably damaging 1.00
R5704:Or6c213 UTSW 10 129,574,685 (GRCm39) missense probably benign 0.00
R6140:Or6c213 UTSW 10 129,574,523 (GRCm39) missense possibly damaging 0.95
R6655:Or6c213 UTSW 10 129,573,956 (GRCm39) missense possibly damaging 0.96
R7647:Or6c213 UTSW 10 129,574,070 (GRCm39) missense probably damaging 0.99
R7879:Or6c213 UTSW 10 129,574,559 (GRCm39) missense probably benign 0.15
R8392:Or6c213 UTSW 10 129,573,910 (GRCm39) missense probably damaging 1.00
R8510:Or6c213 UTSW 10 129,574,054 (GRCm39) missense probably benign 0.01
R8765:Or6c213 UTSW 10 129,574,511 (GRCm39) missense probably damaging 1.00
R8774:Or6c213 UTSW 10 129,573,926 (GRCm39) missense probably damaging 1.00
R8774-TAIL:Or6c213 UTSW 10 129,573,926 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CCTTTGTTGAGCTGAAGGGAAC -3'
(R):5'- TCCACGATTCTTGATGAGCATTC -3'

Sequencing Primer
(F):5'- CTAAGATCAAGGTGATGATAAGTGTC -3'
(R):5'- ACAATTACCTACAATGCTTGTGTAG -3'
Posted On 2018-09-12