Incidental Mutation 'R8931:Or6c33'
ID 680320
Institutional Source Beutler Lab
Gene Symbol Or6c33
Ensembl Gene ENSMUSG00000048745
Gene Name olfactory receptor family 6 subfamily C member 33
Synonyms GA_x6K02T2PULF-11688441-11689379, Olfr820, MOR116-1
MMRRC Submission 068775-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.058) question?
Stock # R8931 (G1)
Quality Score 225.009
Status Validated
Chromosome 10
Chromosomal Location 129853232-129854170 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 129853769 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Serine at position 180 (T180S)
Ref Sequence ENSEMBL: ENSMUSP00000150332 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000059244] [ENSMUST00000214917] [ENSMUST00000215791]
AlphaFold Q8VFU5
Predicted Effect possibly damaging
Transcript: ENSMUST00000059244
AA Change: T180S

PolyPhen 2 Score 0.806 (Sensitivity: 0.84; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000052995
Gene: ENSMUSG00000048745
AA Change: T180S

DomainStartEndE-ValueType
Pfam:7tm_4 29 306 1e-47 PFAM
Pfam:7tm_1 39 288 1.8e-21 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000214917
AA Change: T180S

PolyPhen 2 Score 0.806 (Sensitivity: 0.84; Specificity: 0.93)
Predicted Effect possibly damaging
Transcript: ENSMUST00000215791
AA Change: T180S

PolyPhen 2 Score 0.806 (Sensitivity: 0.84; Specificity: 0.93)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.8%
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: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acat3 G C 17: 13,147,405 (GRCm39) P204R probably damaging Het
Aldh3b1 A G 19: 3,968,803 (GRCm39) I250T possibly damaging Het
Ankrd11 C T 8: 123,622,718 (GRCm39) R378K probably damaging Het
Arap1 G A 7: 101,057,324 (GRCm39) R1355Q possibly damaging Het
Arhgef19 T C 4: 140,976,603 (GRCm39) V455A probably damaging Het
BC051019 T C 7: 109,315,286 (GRCm39) E323G probably damaging Het
Bzw2 T C 12: 36,184,943 (GRCm39) N2S possibly damaging Het
Calm3 G C 7: 16,651,398 (GRCm39) F66L probably damaging Het
Carmil1 T A 13: 24,338,704 (GRCm39) T191S probably benign Het
Cemip2 T A 19: 21,770,323 (GRCm39) S104T probably benign Het
Cep170 A T 1: 176,597,377 (GRCm39) C389S probably benign Het
Clhc1 C T 11: 29,510,533 (GRCm39) Q195* probably null Het
Cttnbp2 A G 6: 18,434,808 (GRCm39) L350P probably benign Het
Cyp7a1 T C 4: 6,271,238 (GRCm39) E306G possibly damaging Het
Ddx25 T C 9: 35,465,864 (GRCm39) N119S possibly damaging Het
Ephx2 G T 14: 66,322,441 (GRCm39) probably benign Het
Ern2 C T 7: 121,769,363 (GRCm39) A888T probably benign Het
Fbln2 A T 6: 91,246,072 (GRCm39) I973F probably damaging Het
Fbn1 T C 2: 125,202,095 (GRCm39) I1259M probably damaging Het
Glis1 A G 4: 107,421,060 (GRCm39) H92R probably benign Het
Gm13283 A C 4: 88,679,516 (GRCm39) D169A probably benign Het
Gpr61 A G 3: 108,057,470 (GRCm39) L397P probably benign Het
H4c11 T A 13: 21,919,369 (GRCm39) I35N probably damaging Het
Hip1 A T 5: 135,460,297 (GRCm39) probably benign Het
Hmgcs2 C T 3: 98,203,557 (GRCm39) A222V probably damaging Het
Ifna2 G A 4: 88,601,712 (GRCm39) T102I probably benign Het
Kat6b T C 14: 21,674,995 (GRCm39) S387P probably damaging Het
Ldlr G A 9: 21,643,108 (GRCm39) V45M probably damaging Het
Mc3r A T 2: 172,091,515 (GRCm39) I246F possibly damaging Het
Mug1 G C 6: 121,861,296 (GRCm39) A1306P probably benign Het
Myo15a A G 11: 60,368,020 (GRCm39) E260G probably benign Het
Naa16 A G 14: 79,582,395 (GRCm39) Y565H probably damaging Het
Ndufaf7 A G 17: 79,244,950 (GRCm39) Y23C possibly damaging Het
Nop58 G A 1: 59,731,549 (GRCm39) probably null Het
Or6c88 A T 10: 129,406,550 (GRCm39) T9S probably benign Het
Or7g19 T A 9: 18,855,920 (GRCm39) probably benign Het
Pcdh8 G A 14: 80,006,971 (GRCm39) Q531* probably null Het
Pik3c2g A G 6: 139,821,093 (GRCm39) T297A probably benign Het
Poc1b T C 10: 99,028,861 (GRCm39) probably null Het
Prb1c G A 6: 132,338,897 (GRCm39) P107L Het
Prokr2 A G 2: 132,215,996 (GRCm39) V155A possibly damaging Het
Rce1 C T 19: 4,674,094 (GRCm39) probably benign Het
Rnf148 A T 6: 23,654,704 (GRCm39) N97K possibly damaging Het
Setbp1 A G 18: 78,899,723 (GRCm39) S1315P probably benign Het
Sgcz A G 8: 38,107,140 (GRCm39) V124A probably damaging Het
Slc25a2 C A 18: 37,771,089 (GRCm39) G147C probably damaging Het
Slc28a2b C A 2: 122,348,983 (GRCm39) P303Q Het
Sod2 T C 17: 13,227,193 (GRCm39) L49P probably damaging Het
Tbc1d12 T C 19: 38,854,098 (GRCm39) V260A probably benign Het
Tcte2 C A 17: 13,933,410 (GRCm39) probably benign Het
Tenm3 T C 8: 48,688,637 (GRCm39) T2317A probably damaging Het
Tfcp2 T C 15: 100,402,298 (GRCm39) I500V possibly damaging Het
Trav14-3 C A 14: 54,001,112 (GRCm39) Q108K probably damaging Het
Trbv14 T C 6: 41,112,364 (GRCm39) Y54H probably damaging Het
Trpm3 T A 19: 22,744,034 (GRCm39) V337E probably damaging Het
Tsbp1 T C 17: 34,659,328 (GRCm39) probably benign Het
Uox A T 3: 146,318,047 (GRCm39) I14F probably damaging Het
Wdfy3 A G 5: 102,065,421 (GRCm39) V1249A probably benign Het
Zfp511 T C 7: 139,617,194 (GRCm39) Y97H probably damaging Het
Zfp536 G T 7: 37,268,721 (GRCm39) Q232K probably benign Het
Zng1 T G 19: 24,932,780 (GRCm39) K84N probably damaging Het
Other mutations in Or6c33
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01387:Or6c33 APN 10 129,853,710 (GRCm39) missense probably damaging 0.98
IGL01938:Or6c33 APN 10 129,853,981 (GRCm39) nonsense probably null
IGL02369:Or6c33 APN 10 129,853,425 (GRCm39) missense possibly damaging 0.81
R0378:Or6c33 UTSW 10 129,853,872 (GRCm39) missense probably damaging 1.00
R0437:Or6c33 UTSW 10 129,853,965 (GRCm39) missense probably damaging 1.00
R0648:Or6c33 UTSW 10 129,853,350 (GRCm39) missense probably damaging 1.00
R1891:Or6c33 UTSW 10 129,853,439 (GRCm39) missense probably damaging 1.00
R2187:Or6c33 UTSW 10 129,853,557 (GRCm39) missense probably damaging 1.00
R4190:Or6c33 UTSW 10 129,853,847 (GRCm39) missense probably damaging 0.96
R4730:Or6c33 UTSW 10 129,853,416 (GRCm39) missense probably damaging 1.00
R6380:Or6c33 UTSW 10 129,853,782 (GRCm39) missense probably benign 0.18
R6496:Or6c33 UTSW 10 129,853,448 (GRCm39) missense probably benign 0.13
R7198:Or6c33 UTSW 10 129,853,760 (GRCm39) missense probably damaging 1.00
R7667:Or6c33 UTSW 10 129,853,403 (GRCm39) missense probably damaging 1.00
R7762:Or6c33 UTSW 10 129,853,050 (GRCm39) intron probably benign
R7823:Or6c33 UTSW 10 129,854,136 (GRCm39) missense probably benign 0.00
R8472:Or6c33 UTSW 10 129,853,445 (GRCm39) missense probably damaging 1.00
R9536:Or6c33 UTSW 10 129,853,345 (GRCm39) missense probably benign 0.01
R9563:Or6c33 UTSW 10 129,853,287 (GRCm39) missense probably benign
R9564:Or6c33 UTSW 10 129,853,287 (GRCm39) missense probably benign
R9565:Or6c33 UTSW 10 129,853,287 (GRCm39) missense probably benign
R9624:Or6c33 UTSW 10 129,853,866 (GRCm39) missense possibly damaging 0.94
R9630:Or6c33 UTSW 10 129,853,410 (GRCm39) missense probably damaging 1.00
R9652:Or6c33 UTSW 10 129,853,809 (GRCm39) missense possibly damaging 0.95
Z1177:Or6c33 UTSW 10 129,853,854 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- AGCAGTGATGTCCTATGACCG -3'
(R):5'- GACCACTATCATGTGAGAGGAAC -3'

Sequencing Primer
(F):5'- CAGTGATGTCCTATGACCGCTATG -3'
(R):5'- TGTGAGAGGAACATGTAGAGAAAGCC -3'
Posted On 2021-08-31