Incidental Mutation 'R6035:Or8b36'
ID 479155
Institutional Source Beutler Lab
Gene Symbol Or8b36
Ensembl Gene ENSMUSG00000094461
Gene Name olfactory receptor family 8 subfamily B member 36
Synonyms MOR162-6, Olfr883, GA_x6K02T2PVTD-31705144-31706073
MMRRC Submission 044207-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.106) question?
Stock # R6035 (G1)
Quality Score 217.468
Status Not validated
Chromosome 9
Chromosomal Location 37937104-37938033 bp(+) (GRCm39)
Type of Mutation frame shift
DNA Base Change (assembly) ATTGCTGTTT to ATTGCTGTTTGCTGTTT at 37937836 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000072741 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000072974]
AlphaFold Q8VF64
Predicted Effect probably null
Transcript: ENSMUST00000072974
SMART Domains Protein: ENSMUSP00000072741
Gene: ENSMUSG00000094461

DomainStartEndE-ValueType
Pfam:7tm_4 31 306 1.6e-48 PFAM
Pfam:7tm_1 41 288 3.7e-24 PFAM
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.8%
  • 3x: 98.9%
  • 10x: 91.8%
  • 20x: 70.9%
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: 80 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2m G T 6: 121,615,353 (GRCm39) G76W probably damaging Het
Abca17 A T 17: 24,500,219 (GRCm39) F1324Y possibly damaging Het
Abca8b A T 11: 109,862,686 (GRCm39) probably null Het
Abcc12 A G 8: 87,244,033 (GRCm39) M1040T probably damaging Het
Abtb1 A G 6: 88,818,788 (GRCm39) F7L probably damaging Het
Adcy9 T C 16: 4,122,377 (GRCm39) T558A probably benign Het
Adgrb1 A T 15: 74,412,292 (GRCm39) T424S possibly damaging Het
Afg3l2 G T 18: 67,554,329 (GRCm39) L458M probably damaging Het
Ankrd31 C A 13: 96,968,721 (GRCm39) P786Q probably benign Het
Arhgap39 G T 15: 76,621,424 (GRCm39) Y392* probably null Het
Ash1l T C 3: 88,892,326 (GRCm39) Y1402H probably damaging Het
Carmil2 G T 8: 106,419,195 (GRCm39) W749L probably benign Het
Ccar1 A G 10: 62,587,564 (GRCm39) Y867H unknown Het
Cdh13 A G 8: 119,232,437 (GRCm39) D47G probably benign Het
Chst9 T A 18: 15,585,910 (GRCm39) T218S probably benign Het
Clec2i G A 6: 128,870,587 (GRCm39) V67I probably benign Het
Cox7a2 T A 9: 79,667,028 (GRCm39) probably benign Het
Cplx3 A G 9: 57,519,030 (GRCm39) probably null Het
Cpz A G 5: 35,674,929 (GRCm39) C107R probably damaging Het
Dapk1 T A 13: 60,909,013 (GRCm39) C1209S possibly damaging Het
Ddx41 T C 13: 55,681,781 (GRCm39) M307V probably benign Het
Defa24 A G 8: 22,224,565 (GRCm39) I5V probably benign Het
Dgcr8 A T 16: 18,076,178 (GRCm39) N2K probably damaging Het
Ebf2 A G 14: 67,476,423 (GRCm39) D131G probably damaging Het
Fam149b C T 14: 20,427,985 (GRCm39) R424C probably damaging Het
Fbln2 G A 6: 91,240,335 (GRCm39) V714M probably damaging Het
Fgf5 T C 5: 98,423,385 (GRCm39) Y257H probably damaging Het
Fmo3 A C 1: 162,791,605 (GRCm39) V224G probably damaging Het
Gigyf2 T C 1: 87,338,450 (GRCm39) I394T possibly damaging Het
Glmn T A 5: 107,741,746 (GRCm39) probably null Het
Greb1l T C 18: 10,501,025 (GRCm39) I385T possibly damaging Het
Grhl1 C A 12: 24,658,449 (GRCm39) Q365K probably benign Het
Gsdme G A 6: 50,206,306 (GRCm39) T179M probably damaging Het
Gtf2a1l A G 17: 89,018,962 (GRCm39) T349A probably benign Het
Hax1 GTCATCATCATCATCATC GTCATCATCATCATCATCATC 3: 89,905,247 (GRCm39) probably benign Het
Il5ra G A 6: 106,718,226 (GRCm39) T76I probably damaging Het
Itga8 T C 2: 12,196,525 (GRCm39) T631A probably benign Het
Kcnh6 G A 11: 105,909,978 (GRCm39) probably null Het
Krt26 C T 11: 99,224,415 (GRCm39) E368K probably benign Het
Lhx9 T C 1: 138,766,281 (GRCm39) D169G possibly damaging Het
Lmod3 A G 6: 97,224,234 (GRCm39) L529P probably damaging Het
Mroh2a G A 1: 88,158,390 (GRCm39) V146M probably damaging Het
Nup155 A G 15: 8,173,577 (GRCm39) T891A probably benign Het
Or11g24 A G 14: 50,661,984 (GRCm39) T3A probably benign Het
Or1e1 T C 11: 73,244,582 (GRCm39) M1T probably null Het
Or1j13 T A 2: 36,369,996 (GRCm39) I49F probably damaging Het
Or1p4-ps1 T C 11: 74,208,285 (GRCm39) *145R probably null Het
Papln G C 12: 83,821,454 (GRCm39) G262A probably damaging Het
Pdcd1lg2 G A 19: 29,423,435 (GRCm39) V160I probably benign Het
Pde8b A G 13: 95,164,105 (GRCm39) probably benign Het
Ppme1 G A 7: 100,004,002 (GRCm39) R68* probably null Het
Ptprn2 A T 12: 117,219,215 (GRCm39) N949Y probably damaging Het
Qser1 C A 2: 104,617,468 (GRCm39) D1115Y probably damaging Het
Rad54l G T 4: 115,954,666 (GRCm39) D674E probably damaging Het
Ripk4 T A 16: 97,545,387 (GRCm39) D420V probably damaging Het
Ros1 G T 10: 51,954,067 (GRCm39) S1857R probably benign Het
Rsf1 ATGGCG ATGGCGACGGTGGCG 7: 97,229,111 (GRCm39) probably benign Het
Rsf1 A G 7: 97,311,316 (GRCm39) E682G probably benign Het
Samd4 G A 14: 47,325,329 (GRCm39) R515H probably damaging Het
Selp T A 1: 163,969,079 (GRCm39) W560R probably benign Het
Shc3 A T 13: 51,615,468 (GRCm39) L163Q probably damaging Het
Shh G A 5: 28,666,397 (GRCm39) A163V probably damaging Het
Slc17a8 T C 10: 89,427,937 (GRCm39) R113G possibly damaging Het
Slc5a6 C A 5: 31,206,168 (GRCm39) probably benign Het
Smarcd2 A G 11: 106,157,715 (GRCm39) probably null Het
Sytl3 A G 17: 6,995,664 (GRCm39) D148G probably damaging Het
Tnks G T 8: 35,385,615 (GRCm39) H297Q possibly damaging Het
Trbv21 A T 6: 41,179,568 (GRCm39) probably benign Het
Ube3c T C 5: 29,806,161 (GRCm39) F268L probably benign Het
Ugt2b5 T C 5: 87,287,541 (GRCm39) I209V probably benign Het
Usp1 A G 4: 98,818,082 (GRCm39) N140S probably damaging Het
Vcam1 T C 3: 115,919,606 (GRCm39) Y226C probably damaging Het
Vmn1r129 T A 7: 21,094,534 (GRCm39) Q228L probably damaging Het
Vmn1r209 T A 13: 22,990,202 (GRCm39) N163Y probably benign Het
Vmn1r85 A G 7: 12,818,854 (GRCm39) S97P probably damaging Het
Vmn2r30 C T 7: 7,337,350 (GRCm39) M95I probably benign Het
Vmn2r74 G A 7: 85,601,098 (GRCm39) R847C probably damaging Het
Wdr70 G A 15: 7,916,830 (GRCm39) T529I possibly damaging Het
Zfp532 T G 18: 65,757,005 (GRCm39) S313A possibly damaging Het
Zhx3 A T 2: 160,621,463 (GRCm39) N901K probably benign Het
Other mutations in Or8b36
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00980:Or8b36 APN 9 37,937,107 (GRCm39) missense probably benign 0.02
IGL02092:Or8b36 APN 9 37,937,917 (GRCm39) missense possibly damaging 0.80
IGL02351:Or8b36 APN 9 37,937,332 (GRCm39) missense possibly damaging 0.78
IGL02358:Or8b36 APN 9 37,937,332 (GRCm39) missense possibly damaging 0.78
IGL02807:Or8b36 APN 9 37,937,485 (GRCm39) missense probably damaging 1.00
R0972:Or8b36 UTSW 9 37,937,856 (GRCm39) missense possibly damaging 0.88
R1016:Or8b36 UTSW 9 37,937,987 (GRCm39) missense probably damaging 0.98
R1818:Or8b36 UTSW 9 37,937,803 (GRCm39) missense probably damaging 1.00
R4466:Or8b36 UTSW 9 37,937,479 (GRCm39) missense probably damaging 0.99
R4871:Or8b36 UTSW 9 37,937,822 (GRCm39) missense probably damaging 1.00
R5977:Or8b36 UTSW 9 37,937,836 (GRCm39) frame shift probably null
R5979:Or8b36 UTSW 9 37,937,836 (GRCm39) frame shift probably null
R6026:Or8b36 UTSW 9 37,937,836 (GRCm39) frame shift probably null
R6027:Or8b36 UTSW 9 37,937,836 (GRCm39) frame shift probably null
R6029:Or8b36 UTSW 9 37,937,836 (GRCm39) frame shift probably null
R6035:Or8b36 UTSW 9 37,937,836 (GRCm39) frame shift probably null
R6053:Or8b36 UTSW 9 37,937,837 (GRCm39) frame shift probably null
R6092:Or8b36 UTSW 9 37,937,836 (GRCm39) frame shift probably null
R6106:Or8b36 UTSW 9 37,937,762 (GRCm39) missense probably damaging 1.00
R6131:Or8b36 UTSW 9 37,937,836 (GRCm39) frame shift probably null
R6132:Or8b36 UTSW 9 37,937,836 (GRCm39) frame shift probably null
R6133:Or8b36 UTSW 9 37,937,836 (GRCm39) frame shift probably null
R6134:Or8b36 UTSW 9 37,937,836 (GRCm39) frame shift probably null
R6153:Or8b36 UTSW 9 37,937,836 (GRCm39) frame shift probably null
R6251:Or8b36 UTSW 9 37,937,842 (GRCm39) frame shift probably null
R6251:Or8b36 UTSW 9 37,937,841 (GRCm39) frame shift probably null
R6251:Or8b36 UTSW 9 37,937,833 (GRCm39) frame shift probably null
R6251:Or8b36 UTSW 9 37,937,844 (GRCm39) frame shift probably null
R6300:Or8b36 UTSW 9 37,937,836 (GRCm39) frame shift probably null
R6301:Or8b36 UTSW 9 37,937,836 (GRCm39) frame shift probably null
R6305:Or8b36 UTSW 9 37,937,838 (GRCm39) frame shift probably null
R6305:Or8b36 UTSW 9 37,937,836 (GRCm39) frame shift probably null
R6307:Or8b36 UTSW 9 37,937,836 (GRCm39) frame shift probably null
R6312:Or8b36 UTSW 9 37,937,842 (GRCm39) frame shift probably null
R6312:Or8b36 UTSW 9 37,937,837 (GRCm39) frame shift probably null
R6312:Or8b36 UTSW 9 37,937,836 (GRCm39) frame shift probably null
R6312:Or8b36 UTSW 9 37,937,845 (GRCm39) frame shift probably null
R6312:Or8b36 UTSW 9 37,937,843 (GRCm39) nonsense probably null
R6813:Or8b36 UTSW 9 37,937,129 (GRCm39) missense probably damaging 1.00
R7134:Or8b36 UTSW 9 37,937,795 (GRCm39) missense probably benign 0.00
R7775:Or8b36 UTSW 9 37,937,963 (GRCm39) missense probably damaging 1.00
R7778:Or8b36 UTSW 9 37,937,963 (GRCm39) missense probably damaging 1.00
R7984:Or8b36 UTSW 9 37,937,155 (GRCm39) missense probably damaging 1.00
R8326:Or8b36 UTSW 9 37,938,014 (GRCm39) missense probably benign 0.00
R9154:Or8b36 UTSW 9 37,937,690 (GRCm39) nonsense probably null
Predicted Primers
Posted On 2017-06-26