Incidental Mutation 'R6194:Or13f5'
ID 502775
Institutional Source Beutler Lab
Gene Symbol Or13f5
Ensembl Gene ENSMUSG00000089717
Gene Name olfactory receptor family 13 subfamily F member 5
Synonyms GA_x6K02T2N78B-7168533-7167574, Olfr275, MOR262-2
MMRRC Submission 044334-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.085) question?
Stock # R6194 (G1)
Quality Score 225.009
Status Not validated
Chromosome 4
Chromosomal Location 52825399-52826358 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 52825779 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Stop codon at position 127 (C127*)
Ref Sequence ENSEMBL: ENSMUSP00000092700 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000095085]
AlphaFold Q7TS18
Predicted Effect probably null
Transcript: ENSMUST00000095085
AA Change: C127*
SMART Domains Protein: ENSMUSP00000092700
Gene: ENSMUSG00000089717
AA Change: C127*

DomainStartEndE-ValueType
Pfam:7tm_4 30 308 9.8e-54 PFAM
Pfam:7tm_1 41 290 6.2e-20 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000120435
Predicted Effect noncoding transcript
Transcript: ENSMUST00000135738
Predicted Effect noncoding transcript
Transcript: ENSMUST00000219705
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.5%
  • 20x: 98.6%
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: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
5031410I06Rik T C 5: 26,309,033 (GRCm39) I90V probably benign Het
Afap1l2 T A 19: 56,911,383 (GRCm39) R370S probably damaging Het
Alcam A G 16: 52,088,761 (GRCm39) Y537H probably damaging Het
Araf G T X: 20,726,339 (GRCm39) R601L probably damaging Homo
Asap1 A G 15: 64,001,058 (GRCm39) S508P probably damaging Het
Atg5 T C 10: 44,170,612 (GRCm39) L86P probably damaging Het
Atp13a5 G A 16: 29,127,057 (GRCm39) P502S probably damaging Het
AW209491 T A 13: 14,811,705 (GRCm39) I186K possibly damaging Het
Baz1b T C 5: 135,272,744 (GRCm39) Y1354H probably damaging Het
Card6 A T 15: 5,127,926 (GRCm39) S1157T unknown Het
Chil6 A G 3: 106,312,192 (GRCm39) probably null Het
Chrna1 A G 2: 73,400,816 (GRCm39) V238A probably benign Het
Cluap1 A G 16: 3,747,770 (GRCm39) S308G probably benign Het
Cntnap4 A G 8: 113,602,061 (GRCm39) D1155G probably damaging Het
Cptp A G 4: 155,951,098 (GRCm39) F123L probably damaging Het
Elapor1 T C 3: 108,373,095 (GRCm39) I600V probably benign Het
Fbxw2 G A 2: 34,697,416 (GRCm39) T317I probably damaging Het
Gc A T 5: 89,589,438 (GRCm39) V197E probably benign Het
Gusb C T 5: 130,018,906 (GRCm39) V577M possibly damaging Het
Hectd1 A T 12: 51,795,228 (GRCm39) N2400K probably damaging Het
Hnrnph1 T A 11: 50,274,104 (GRCm39) D340E possibly damaging Het
Hs3st1 C A 5: 39,771,748 (GRCm39) K298N probably damaging Het
Hunk A T 16: 90,293,283 (GRCm39) T522S probably damaging Het
Ifit3 T C 19: 34,565,027 (GRCm39) F191S probably benign Het
Ifnab T A 4: 88,609,362 (GRCm39) K35* probably null Het
Ifnab G T 4: 88,609,363 (GRCm39) N34K probably damaging Het
Ighmbp2 C A 19: 3,312,003 (GRCm39) R917L possibly damaging Het
Igkv13-84 C T 6: 68,916,916 (GRCm39) A71V possibly damaging Het
Irag1 T C 7: 110,498,901 (GRCm39) N377D probably damaging Het
Lim2 T A 7: 43,085,086 (GRCm39) C159S probably damaging Het
Lrrc56 T C 7: 140,785,564 (GRCm39) Y147H probably damaging Het
Ltn1 A G 16: 87,212,698 (GRCm39) L621P probably damaging Het
Mapk8ip1 C A 2: 92,219,589 (GRCm39) G81C probably damaging Het
Mboat2 T A 12: 24,996,637 (GRCm39) S213R probably benign Het
Mmel1 T A 4: 154,967,673 (GRCm39) C99* probably null Het
Myo9a A G 9: 59,777,033 (GRCm39) I1144V probably benign Het
Naa15 A G 3: 51,370,721 (GRCm39) T612A probably benign Het
Naalad2 C T 9: 18,262,443 (GRCm39) V362I probably benign Het
Nbeal1 A T 1: 60,296,643 (GRCm39) I1178F possibly damaging Het
Nras C A 3: 102,966,269 (GRCm39) A11E probably damaging Het
Or56a3b G T 7: 104,771,377 (GRCm39) V238L probably benign Het
Pcdhb7 A G 18: 37,475,199 (GRCm39) T112A probably damaging Het
Peg10 C CCCATCAGGA 6: 4,756,351 (GRCm39) probably benign Het
Pfkfb2 A G 1: 130,625,624 (GRCm39) *519Q probably null Het
Prodh A T 16: 17,890,381 (GRCm39) H515Q probably benign Het
Rbfox2 T C 15: 76,968,357 (GRCm39) T435A possibly damaging Het
Rbks T C 5: 31,824,234 (GRCm39) E87G probably benign Het
Scyl1 G T 19: 5,820,334 (GRCm39) Q167K possibly damaging Het
Serpina3i T A 12: 104,232,762 (GRCm39) D222E probably benign Het
Slc36a4 T A 9: 15,638,172 (GRCm39) C199* probably null Het
Slx1b C T 7: 126,291,503 (GRCm39) R187H possibly damaging Het
Stxbp5 A G 10: 9,693,083 (GRCm39) F348L probably damaging Het
Tbc1d2 C T 4: 46,629,912 (GRCm39) G252R probably benign Het
Tfpt A T 7: 3,632,026 (GRCm39) L28Q probably damaging Het
Trap1 G A 16: 3,872,664 (GRCm39) T335M possibly damaging Het
Zcchc2 T A 1: 105,918,847 (GRCm39) F110I probably damaging Het
Zfp345 A T 2: 150,314,551 (GRCm39) C329S probably damaging Het
Other mutations in Or13f5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01108:Or13f5 APN 4 52,825,727 (GRCm39) missense probably damaging 1.00
IGL01758:Or13f5 APN 4 52,825,468 (GRCm39) nonsense probably null
IGL01925:Or13f5 APN 4 52,825,910 (GRCm39) missense probably benign 0.00
IGL02525:Or13f5 APN 4 52,825,616 (GRCm39) missense probably damaging 1.00
IGL02536:Or13f5 APN 4 52,825,817 (GRCm39) missense possibly damaging 0.95
IGL02829:Or13f5 APN 4 52,826,027 (GRCm39) missense probably damaging 0.98
R0068:Or13f5 UTSW 4 52,825,503 (GRCm39) nonsense probably null
R0068:Or13f5 UTSW 4 52,825,503 (GRCm39) nonsense probably null
R0190:Or13f5 UTSW 4 52,825,613 (GRCm39) missense probably damaging 0.97
R4376:Or13f5 UTSW 4 52,826,195 (GRCm39) missense possibly damaging 0.81
R4617:Or13f5 UTSW 4 52,825,399 (GRCm39) start codon destroyed probably benign 0.35
R4658:Or13f5 UTSW 4 52,826,240 (GRCm39) missense probably damaging 0.99
R4828:Or13f5 UTSW 4 52,826,138 (GRCm39) missense probably damaging 1.00
R4850:Or13f5 UTSW 4 52,825,450 (GRCm39) missense possibly damaging 0.94
R6401:Or13f5 UTSW 4 52,826,242 (GRCm39) missense probably damaging 1.00
R6842:Or13f5 UTSW 4 52,825,576 (GRCm39) missense probably damaging 1.00
R7033:Or13f5 UTSW 4 52,826,089 (GRCm39) missense probably benign
R7998:Or13f5 UTSW 4 52,825,970 (GRCm39) missense possibly damaging 0.89
R8101:Or13f5 UTSW 4 52,825,849 (GRCm39) missense probably benign 0.03
R9655:Or13f5 UTSW 4 52,825,526 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- AGCAACCTCTCATTTCTGGAC -3'
(R):5'- ACTGTACCATGGAAGTGTCTC -3'

Sequencing Primer
(F):5'- GGACATCTGGTATACCTCTTCTG -3'
(R):5'- TGTACCATGGAAGTGTCTCCACAG -3'
Posted On 2018-02-27