Incidental Mutation 'R6835:Or1e31'
ID 534408
Institutional Source Beutler Lab
Gene Symbol Or1e31
Ensembl Gene ENSMUSG00000070382
Gene Name olfactory receptor family 1 subfamily E member 31
Synonyms MOR135-24, Olfr391, Olfr391-ps1, Olfr391-ps, GA_x6K02T2P1NL-3951666-3950698, MOR135-30_i
MMRRC Submission 044944-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.113) question?
Stock # R6835 (G1)
Quality Score 225.009
Status Validated
Chromosome 11
Chromosomal Location 73689579-73693810 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 73690061 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Threonine at position 174 (I174T)
Ref Sequence ENSEMBL: ENSMUSP00000151029 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000214485]
AlphaFold A0A0U1RNJ4
Predicted Effect possibly damaging
Transcript: ENSMUST00000214485
AA Change: I174T

PolyPhen 2 Score 0.948 (Sensitivity: 0.79; Specificity: 0.95)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.5%
  • 20x: 98.2%
Validation Efficiency 100% (44/44)
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: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actl11 A G 9: 107,807,761 (GRCm39) R695G probably benign Het
Arhgef4 A G 1: 34,845,574 (GRCm39) H1533R probably damaging Het
Birc6 T C 17: 74,949,499 (GRCm39) L3120P probably damaging Het
Cfap46 T A 7: 139,232,414 (GRCm39) I850F probably damaging Het
Crym A C 7: 119,785,868 (GRCm39) S311A probably benign Het
Cttn T C 7: 144,010,234 (GRCm39) probably null Het
Dtnb C T 12: 3,682,841 (GRCm39) probably benign Het
Edem1 T C 6: 108,831,360 (GRCm39) V607A probably benign Het
Etfa A G 9: 55,403,103 (GRCm39) V64A probably benign Het
Fam133b A G 5: 3,604,732 (GRCm39) T40A possibly damaging Het
Fmn2 C A 1: 174,527,235 (GRCm39) D1442E probably damaging Het
Gpi1 T C 7: 33,926,563 (GRCm39) K128E possibly damaging Het
Gpr179 A T 11: 97,238,293 (GRCm39) F310L probably damaging Het
Hdac7 T A 15: 97,700,628 (GRCm39) H531L probably damaging Het
Hfm1 G A 5: 107,026,681 (GRCm39) R145* probably null Het
Hsp90b1 A T 10: 86,529,949 (GRCm39) D573E probably damaging Het
Hunk T G 16: 90,269,412 (GRCm39) W243G probably damaging Het
Icam1 G T 9: 20,938,421 (GRCm39) G327W possibly damaging Het
Ino80d C A 1: 63,113,485 (GRCm39) A322S probably benign Het
Irag1 T G 7: 110,520,541 (GRCm39) E278A probably damaging Het
Itpkc A C 7: 26,927,240 (GRCm39) S225A probably benign Het
Krt75 C T 15: 101,479,472 (GRCm39) R286Q probably benign Het
Lmnb2 A G 10: 80,745,794 (GRCm39) L95P probably damaging Het
Mns1 T C 9: 72,360,026 (GRCm39) M392T probably damaging Het
Morc3 A T 16: 93,644,309 (GRCm39) N200I probably damaging Het
Myadm T C 7: 3,346,192 (GRCm39) V318A possibly damaging Het
Nt5dc1 A C 10: 34,186,375 (GRCm39) S398A probably benign Het
Or13c7 T C 4: 43,854,912 (GRCm39) V201A probably benign Het
Pcdhga2 T C 18: 37,803,842 (GRCm39) I562T probably damaging Het
Pcdhgb1 T A 18: 37,813,553 (GRCm39) C15S probably benign Het
Pikfyve T G 1: 65,298,002 (GRCm39) L1532R probably damaging Het
Rdh7 T A 10: 127,720,608 (GRCm39) T255S probably benign Het
Rtel1 A G 2: 180,997,746 (GRCm39) T1165A probably benign Het
Sdk2 C T 11: 113,720,874 (GRCm39) A1352T probably damaging Het
Strip2 T C 6: 29,941,916 (GRCm39) S629P probably damaging Het
Taf5 A G 19: 47,065,776 (GRCm39) T494A possibly damaging Het
Tek T G 4: 94,741,671 (GRCm39) N809K possibly damaging Het
Tmbim7 A T 5: 3,711,943 (GRCm39) T63S probably benign Het
Utrn A T 10: 12,603,508 (GRCm39) L624Q probably damaging Het
Xbp1 A G 11: 5,471,809 (GRCm39) probably benign Het
Zbp1 T A 2: 173,055,704 (GRCm39) probably null Het
Zfp112 T C 7: 23,825,231 (GRCm39) C400R probably damaging Het
Zfp202 C T 9: 40,121,531 (GRCm39) probably null Het
Zfp747 T C 7: 126,973,219 (GRCm39) E317G possibly damaging Het
Other mutations in Or1e31
AlleleSourceChrCoordTypePredicted EffectPPH Score
R2967:Or1e31 UTSW 11 73,689,933 (GRCm39) missense possibly damaging 0.95
R4782:Or1e31 UTSW 11 73,689,665 (GRCm39) missense probably benign 0.00
R5011:Or1e31 UTSW 11 73,690,473 (GRCm39) missense possibly damaging 0.56
R5984:Or1e31 UTSW 11 73,690,407 (GRCm39) missense possibly damaging 0.95
R6276:Or1e31 UTSW 11 73,690,229 (GRCm39) missense probably damaging 1.00
R6338:Or1e31 UTSW 11 73,690,145 (GRCm39) missense possibly damaging 0.93
R6968:Or1e31 UTSW 11 73,690,205 (GRCm39) missense possibly damaging 0.86
R7125:Or1e31 UTSW 11 73,689,990 (GRCm39) missense probably benign 0.00
R7258:Or1e31 UTSW 11 73,690,206 (GRCm39) missense probably damaging 0.98
R7272:Or1e31 UTSW 11 73,689,695 (GRCm39) missense probably damaging 1.00
R7665:Or1e31 UTSW 11 73,689,787 (GRCm39) missense probably benign 0.03
R8053:Or1e31 UTSW 11 73,689,822 (GRCm39) missense probably benign 0.22
R8314:Or1e31 UTSW 11 73,690,568 (GRCm39) missense noncoding transcript
R9089:Or1e31 UTSW 11 73,690,052 (GRCm39) missense probably damaging 1.00
R9328:Or1e31 UTSW 11 73,690,478 (GRCm39) missense probably damaging 1.00
R9788:Or1e31 UTSW 11 73,689,768 (GRCm39) missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- CAAGGTCACCACAGACAGATGG -3'
(R):5'- CATGGCCTATGACCGCTATGTG -3'

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