Incidental Mutation 'R6251:Or8b36'
ID 506227
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 044368-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.106) question?
Stock # R6251 (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) G to GGGATTGC at 37937833 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
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.6%
  • 20x: 96.3%
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: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3100002H09Rik A G 4: 124,504,445 (GRCm39) S36P probably damaging Het
Agmo A G 12: 37,302,538 (GRCm39) D125G probably damaging Het
Arhgap26 A T 18: 39,490,880 (GRCm39) S328C probably null Het
Arl6 T C 16: 59,439,169 (GRCm39) D175G probably damaging Het
Asb3 G A 11: 31,005,559 (GRCm39) A192T probably damaging Het
Atp10b A T 11: 43,126,573 (GRCm39) M1110L possibly damaging Het
Cacna1i T C 15: 80,220,883 (GRCm39) I175T probably damaging Het
Car15 A T 16: 17,655,227 (GRCm39) I71N probably benign Het
Casq1 T A 1: 172,044,407 (GRCm39) Y140F probably benign Het
Ccdc93 C T 1: 121,362,269 (GRCm39) T17M possibly damaging Het
Cfap46 CCTTCTTCT CCTTCT 7: 139,218,816 (GRCm39) probably benign Het
Ciart G A 3: 95,788,323 (GRCm39) probably benign Het
Cul5 A T 9: 53,558,094 (GRCm39) V170D probably benign Het
Cyb5r3 T C 15: 83,038,917 (GRCm39) D224G probably benign Het
Daam1 G A 12: 72,035,723 (GRCm39) G964R probably damaging Het
Daglb T A 5: 143,475,689 (GRCm39) L383Q probably damaging Het
Dazap2 T G 15: 100,514,864 (GRCm39) H28Q possibly damaging Het
Dnttip2 A T 3: 122,068,905 (GRCm39) D40V probably benign Het
Dynlt2b T A 16: 32,245,727 (GRCm39) D125E possibly damaging Het
Epn1 G T 7: 5,098,925 (GRCm39) D406Y probably damaging Het
Epn1 G T 7: 5,098,935 (GRCm39) R409L probably damaging Het
Evc T C 5: 37,457,843 (GRCm39) T966A probably benign Het
Extl3 T C 14: 65,314,375 (GRCm39) D269G probably damaging Het
Gfra3 TGCGC TGC 18: 34,828,864 (GRCm39) probably null Het
Gpr87 A T 3: 59,086,528 (GRCm39) F326I probably damaging Het
Hivep3 C A 4: 119,952,137 (GRCm39) P151H probably damaging Het
Kcnj14 T A 7: 45,467,440 (GRCm39) E302V probably damaging Het
Kdm5d T C Y: 921,693 (GRCm39) Y534H probably damaging Homo
Map3k5 T A 10: 20,014,006 (GRCm39) probably null Het
Mdn1 A G 4: 32,748,590 (GRCm39) T4212A probably benign Het
Ms4a6d A T 19: 11,564,504 (GRCm39) S122R probably damaging Het
Mtarc1 G A 1: 184,527,648 (GRCm39) R271W probably damaging Het
Nectin3 A T 16: 46,215,513 (GRCm39) H76Q probably damaging Het
Notch1 C A 2: 26,364,182 (GRCm39) E846D possibly damaging Het
Or1e23 A G 11: 73,407,534 (GRCm39) S164P probably benign Het
Or4a67 T C 2: 88,598,632 (GRCm39) E9G probably damaging Het
Or8g18 T A 9: 39,149,514 (GRCm39) I72F possibly damaging Het
Pfkl C T 10: 77,825,399 (GRCm39) probably null Het
Pigz T C 16: 31,764,424 (GRCm39) V494A possibly damaging Het
Pik3r4 T C 9: 105,531,247 (GRCm39) V516A probably benign Het
Polr2b G A 5: 77,496,141 (GRCm39) R1104K probably benign Het
Rap1a A T 3: 105,639,311 (GRCm39) L116* probably null Het
Rnf114 T C 2: 167,356,649 (GRCm39) *230R probably null Het
Rtl1 G T 12: 109,560,083 (GRCm39) N585K probably benign Het
Serpinb5 G T 1: 106,802,795 (GRCm39) R110I possibly damaging Het
Spink6 T C 18: 44,207,498 (GRCm39) probably null Het
Spopfm1 G T 3: 94,173,208 (GRCm39) S72I probably damaging Het
Stk39 A T 2: 68,137,383 (GRCm39) probably null Het
Tcstv2a T C 13: 120,724,907 (GRCm39) probably benign Het
Tcte1 A T 17: 45,846,085 (GRCm39) T230S probably benign Het
Tecpr1 C A 5: 144,135,394 (GRCm39) V1020L probably damaging Het
Tmc7 T C 7: 118,160,261 (GRCm39) Y192C possibly damaging Het
Trim63 A T 4: 134,050,537 (GRCm39) T274S probably benign Het
Wdr43 G A 17: 71,957,048 (GRCm39) probably null Het
Zfr T C 15: 12,160,677 (GRCm39) I750T 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
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 37,937,844 (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
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 PCR Primer
(F):5'- TGACCTTCTGTGATGGCAAC -3'
(R):5'- TCTAAGTGCAAGGTAGACATCC -3'

Sequencing Primer
(F):5'- ATCACTATGCATGTGACATACTTCC -3'
(R):5'- GTGCAAGGTAGACATCCTTATTCC -3'
Posted On 2018-03-15