Incidental Mutation 'R1066:Or5b113'
ID 86030
Institutional Source Beutler Lab
Gene Symbol Or5b113
Ensembl Gene ENSMUSG00000049015
Gene Name olfactory receptor family 5 subfamily B member 113
Synonyms GA_x6K02T2RE5P-3695694-3696620, Olfr1467, MOR202-15
MMRRC Submission 039152-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.091) question?
Stock # R1066 (G1)
Quality Score 225
Status Not validated
Chromosome 19
Chromosomal Location 13341994-13342920 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 13342451 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Threonine at position 153 (M153T)
Ref Sequence ENSEMBL: ENSMUSP00000149487 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000054687] [ENSMUST00000215096]
AlphaFold Q8VFW1
Predicted Effect probably benign
Transcript: ENSMUST00000054687
AA Change: M153T

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000061580
Gene: ENSMUSG00000049015
AA Change: M153T

DomainStartEndE-ValueType
Pfam:7tm_4 30 307 6.6e-48 PFAM
Pfam:7tm_1 40 289 7.4e-20 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000215096
AA Change: M153T

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.1%
  • 20x: 94.1%
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: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts8 T A 9: 30,867,837 (GRCm39) C554S probably damaging Het
Adarb2 T G 13: 8,807,359 (GRCm39) F720C probably benign Het
Arid5b T C 10: 67,934,186 (GRCm39) D572G probably benign Het
BB014433 C T 8: 15,092,185 (GRCm39) V223M probably damaging Het
Boc T C 16: 44,311,047 (GRCm39) probably null Het
Brf2 T C 8: 27,613,974 (GRCm39) E404G probably benign Het
Ces3a T A 8: 105,782,288 (GRCm39) H380Q probably benign Het
Chd9 T A 8: 91,712,764 (GRCm39) Y389* probably null Het
Csmd3 A G 15: 47,777,361 (GRCm39) F1182L probably damaging Het
Dnah2 C A 11: 69,338,645 (GRCm39) W3169L probably damaging Het
Dnah3 T A 7: 119,660,232 (GRCm39) E802D probably damaging Het
Dtx4 G T 19: 12,478,373 (GRCm39) T70K probably damaging Het
Fat4 T C 3: 39,011,376 (GRCm39) Y2159H probably damaging Het
Flrt2 T A 12: 95,745,833 (GRCm39) V57E probably damaging Het
Gsdmc2 T A 15: 63,696,899 (GRCm39) Y424F possibly damaging Het
Igfn1 T C 1: 135,898,463 (GRCm39) E701G probably benign Het
Klhl42 T C 6: 147,009,397 (GRCm39) V412A probably benign Het
Mkln1 A C 6: 31,395,922 (GRCm39) N52T possibly damaging Het
Msantd5f6 C A 4: 73,320,066 (GRCm39) V238L possibly damaging Het
Myo15b A T 11: 115,770,577 (GRCm39) M1519L probably benign Het
Nup155 A T 15: 8,187,244 (GRCm39) H1391L probably damaging Het
P4ha3 G T 7: 99,967,270 (GRCm39) V360L possibly damaging Het
Pals2 A T 6: 50,122,847 (GRCm39) N31I possibly damaging Het
Phf14 T A 6: 11,987,254 (GRCm39) D611E possibly damaging Het
Pik3r1 T A 13: 101,825,171 (GRCm39) R465S probably damaging Het
Reep3 G T 10: 66,870,445 (GRCm39) T117K probably damaging Het
Reln G T 5: 22,239,662 (GRCm39) N868K probably damaging Het
Sdcbp T G 4: 6,385,120 (GRCm39) I113S probably damaging Het
Sema4c A T 1: 36,589,281 (GRCm39) V615E possibly damaging Het
Slc25a18 A G 6: 120,765,249 (GRCm39) probably null Het
Tedc2 T A 17: 24,435,291 (GRCm39) E366V probably damaging Het
Tedc2 C A 17: 24,435,292 (GRCm39) E366* probably null Het
Uba2 A T 7: 33,858,247 (GRCm39) F70I probably damaging Het
Usp42 A T 5: 143,703,796 (GRCm39) H422Q probably damaging Het
Vmn2r86 C T 10: 130,282,145 (GRCm39) V824I probably benign Het
Vps50 A C 6: 3,533,565 (GRCm39) T266P probably damaging Het
Znhit6 T A 3: 145,284,252 (GRCm39) D141E probably damaging Het
Other mutations in Or5b113
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00936:Or5b113 APN 19 13,341,988 (GRCm39) utr 5 prime probably benign
IGL01109:Or5b113 APN 19 13,342,063 (GRCm39) missense probably benign
IGL01939:Or5b113 APN 19 13,342,807 (GRCm39) missense probably benign 0.14
IGL02188:Or5b113 APN 19 13,342,643 (GRCm39) missense probably damaging 0.98
IGL02188:Or5b113 APN 19 13,342,396 (GRCm39) missense probably benign 0.39
IGL03223:Or5b113 APN 19 13,342,645 (GRCm39) missense probably benign
R0456:Or5b113 UTSW 19 13,342,102 (GRCm39) missense probably damaging 0.98
R1189:Or5b113 UTSW 19 13,342,543 (GRCm39) missense probably benign 0.03
R1668:Or5b113 UTSW 19 13,342,234 (GRCm39) missense probably benign 0.00
R1754:Or5b113 UTSW 19 13,342,717 (GRCm39) missense probably damaging 1.00
R1860:Or5b113 UTSW 19 13,342,705 (GRCm39) missense possibly damaging 0.80
R1861:Or5b113 UTSW 19 13,342,705 (GRCm39) missense possibly damaging 0.80
R2181:Or5b113 UTSW 19 13,342,438 (GRCm39) missense probably benign 0.08
R2219:Or5b113 UTSW 19 13,342,901 (GRCm39) missense possibly damaging 0.88
R2516:Or5b113 UTSW 19 13,342,557 (GRCm39) nonsense probably null
R4757:Or5b113 UTSW 19 13,342,810 (GRCm39) missense probably benign 0.23
R5206:Or5b113 UTSW 19 13,342,429 (GRCm39) missense possibly damaging 0.91
R5376:Or5b113 UTSW 19 13,342,762 (GRCm39) missense possibly damaging 0.95
R5647:Or5b113 UTSW 19 13,342,541 (GRCm39) missense probably damaging 1.00
R5724:Or5b113 UTSW 19 13,342,515 (GRCm39) missense possibly damaging 0.62
R5741:Or5b113 UTSW 19 13,342,847 (GRCm39) missense probably damaging 0.97
R5906:Or5b113 UTSW 19 13,342,369 (GRCm39) missense probably damaging 1.00
R6636:Or5b113 UTSW 19 13,342,589 (GRCm39) missense probably benign 0.06
R6637:Or5b113 UTSW 19 13,342,589 (GRCm39) missense probably benign 0.06
R7000:Or5b113 UTSW 19 13,341,987 (GRCm39) start gained probably benign
R7254:Or5b113 UTSW 19 13,342,475 (GRCm39) missense probably benign 0.28
R7325:Or5b113 UTSW 19 13,342,001 (GRCm39) missense probably benign 0.00
R7773:Or5b113 UTSW 19 13,342,598 (GRCm39) missense probably benign 0.07
R7828:Or5b113 UTSW 19 13,342,510 (GRCm39) missense probably benign 0.10
R9081:Or5b113 UTSW 19 13,342,019 (GRCm39) missense probably benign 0.12
R9135:Or5b113 UTSW 19 13,342,755 (GRCm39) missense possibly damaging 0.46
R9151:Or5b113 UTSW 19 13,342,222 (GRCm39) missense possibly damaging 0.95
R9470:Or5b113 UTSW 19 13,342,115 (GRCm39) missense probably damaging 1.00
R9792:Or5b113 UTSW 19 13,342,514 (GRCm39) missense probably damaging 0.99
R9793:Or5b113 UTSW 19 13,342,514 (GRCm39) missense probably damaging 0.99
Z1176:Or5b113 UTSW 19 13,342,280 (GRCm39) missense probably damaging 1.00
Z1176:Or5b113 UTSW 19 13,342,279 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TTCCTACAATGACTGTGCTGCTCAG -3'
(R):5'- TCAAGCTGTAGACCAGAGGGTTCAG -3'

Sequencing Primer
(F):5'- ACTGTGCTGCTCAGATGTTC -3'
(R):5'- ATTGCATCTTCACGATGGTGAC -3'
Posted On 2013-11-18