Incidental Mutation 'R8508:Olfr1501'
ID655733
Institutional Source Beutler Lab
Gene Symbol Olfr1501
Ensembl Gene ENSMUSG00000057270
Gene Nameolfactory receptor 1501
SynonymsGA_x6K02T2RE5P-4171358-4170411, MOR212-3
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.094) question?
Stock #R8508 (G1)
Quality Score225.009
Status Not validated
Chromosome19
Chromosomal Location13835033-13850692 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 13838402 bp
ZygosityHeterozygous
Amino Acid Change Methionine to Lysine at position 257 (M257K)
Ref Sequence ENSEMBL: ENSMUSP00000147096 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000073966] [ENSMUST00000208493] [ENSMUST00000215350]
Predicted Effect possibly damaging
Transcript: ENSMUST00000073966
AA Change: M257K

PolyPhen 2 Score 0.802 (Sensitivity: 0.84; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000073620
Gene: ENSMUSG00000057270
AA Change: M257K

DomainStartEndE-ValueType
Pfam:7tm_4 30 307 1.8e-45 PFAM
Pfam:7tm_1 40 306 7.1e-18 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000208493
AA Change: M257K

PolyPhen 2 Score 0.802 (Sensitivity: 0.84; Specificity: 0.93)
Predicted Effect possibly damaging
Transcript: ENSMUST00000215350
AA Change: M257K

PolyPhen 2 Score 0.802 (Sensitivity: 0.84; Specificity: 0.93)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.5%
  • 20x: 98.0%
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: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700014D04Rik A G 13: 59,743,598 L136P probably benign Het
4932438H23Rik T G 16: 91,055,612 Y212S probably damaging Het
Angpt1 T C 15: 42,512,399 N154D probably damaging Het
Angpt2 G A 8: 18,741,119 R54* probably null Het
Ankrd27 T A 7: 35,601,626 L117* probably null Het
Arhgap21 C T 2: 20,854,180 M1234I probably benign Het
Arhgef33 A G 17: 80,367,335 E387G probably damaging Het
Atp13a4 T A 16: 29,454,769 K444* probably null Het
Atp6v1a G A 16: 44,101,862 R338C probably damaging Het
Canx T C 11: 50,311,647 D44G possibly damaging Het
Ccdc141 T A 2: 77,132,244 M119L probably benign Het
Ckmt1 A C 2: 121,362,691 Q299P possibly damaging Het
Dhx16 T C 17: 35,885,920 S601P probably damaging Het
Dna2 A C 10: 62,950,894 R140S probably damaging Het
Dock1 A G 7: 134,782,409 T670A probably benign Het
Eogt A G 6: 97,143,998 S85P possibly damaging Het
Fbf1 A T 11: 116,165,881 M1K probably null Het
Fbxl12 C A 9: 20,638,864 R165L possibly damaging Het
Flnb G A 14: 7,950,394 V2571I probably damaging Het
Gm11361 A G 13: 28,257,711 I26V probably benign Het
Gm43518 A G 5: 123,938,259 E123G unknown Het
Gm8332 T G 12: 88,249,685 E139A unknown Het
Gpatch2 A G 1: 187,304,355 N374S probably benign Het
Hey1 G C 3: 8,664,776 A207G probably benign Het
Hoxa11 T C 6: 52,245,802 probably benign Het
Hydin G A 8: 110,582,018 V3979I probably benign Het
Ighe C T 12: 113,271,793 W277* probably null Het
Kmt2c G T 5: 25,314,122 T2330K probably benign Het
Krt6a T A 15: 101,692,735 K261M probably damaging Het
Lats2 A C 14: 57,722,705 S161A probably benign Het
Med13l T A 5: 118,754,321 D1936E probably benign Het
Mipol1 T C 12: 57,306,088 V71A possibly damaging Het
Mphosph8 A T 14: 56,676,546 K415* probably null Het
Npepps A G 11: 97,244,426 probably null Het
Ntn4 A T 10: 93,741,104 N545Y possibly damaging Het
Olfr164 T C 16: 19,286,701 D14G probably benign Het
Olfr353 A G 2: 36,890,354 S165P probably damaging Het
Olfr738 A C 14: 50,413,675 M44L probably benign Het
Osbpl2 T A 2: 180,155,343 V358E possibly damaging Het
Pdcd11 C A 19: 47,119,806 P1204Q probably damaging Het
Pnliprp2 A C 19: 58,763,374 S184R probably damaging Het
Ppm1g G T 5: 31,204,528 R373S probably damaging Het
Rnf130 A G 11: 50,087,437 D275G probably damaging Het
Setd5 T C 6: 113,121,087 S696P probably damaging Het
Sgip1 A G 4: 102,915,071 Q219R probably benign Het
Slc1a2 T C 2: 102,736,085 probably null Het
Slc22a12 T C 19: 6,542,437 T106A probably benign Het
Slc22a14 A G 9: 119,180,585 L148P probably damaging Het
Slc2a9 A T 5: 38,382,078 F375I probably damaging Het
Sorbs3 A T 14: 70,202,947 D117E probably benign Het
Sphkap G A 1: 83,276,500 T1176I probably damaging Het
Supt16 A T 14: 52,181,589 V193D probably damaging Het
Sytl3 A G 17: 6,728,291 T362A probably damaging Het
Tctn1 T A 5: 122,246,611 Q410L probably benign Het
Trbc2 T C 6: 41,547,777 Y133H Het
Ttc28 G A 5: 111,233,341 D1240N probably benign Het
Vmn2r120 A G 17: 57,525,843 V112A probably benign Het
Zfp354b A T 11: 50,923,470 S209R probably benign Het
Zfp362 T C 4: 128,774,606 H391R probably damaging Het
Other mutations in Olfr1501
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01395:Olfr1501 APN 19 13838952 missense probably damaging 0.98
IGL01724:Olfr1501 APN 19 13838861 missense probably damaging 1.00
IGL02075:Olfr1501 APN 19 13838466 missense probably damaging 0.99
IGL02179:Olfr1501 APN 19 13838487 missense probably benign 0.01
IGL02410:Olfr1501 APN 19 13839131 missense probably benign
IGL02927:Olfr1501 APN 19 13838924 missense probably benign 0.05
R0234:Olfr1501 UTSW 19 13838538 missense possibly damaging 0.62
R0234:Olfr1501 UTSW 19 13838538 missense possibly damaging 0.62
R2149:Olfr1501 UTSW 19 13838582 missense probably damaging 1.00
R3442:Olfr1501 UTSW 19 13839006 missense possibly damaging 0.92
R3922:Olfr1501 UTSW 19 13838766 missense probably damaging 1.00
R3924:Olfr1501 UTSW 19 13838766 missense probably damaging 1.00
R4856:Olfr1501 UTSW 19 13838279 missense probably damaging 0.99
R4886:Olfr1501 UTSW 19 13838279 missense probably damaging 0.99
R5175:Olfr1501 UTSW 19 13838316 missense probably damaging 1.00
R5636:Olfr1501 UTSW 19 13838337 missense possibly damaging 0.78
R5716:Olfr1501 UTSW 19 13838639 missense probably damaging 1.00
R6080:Olfr1501 UTSW 19 13839100 missense possibly damaging 0.76
R6849:Olfr1501 UTSW 19 13838839 nonsense probably null
R7011:Olfr1501 UTSW 19 13839039 missense probably benign 0.04
R8223:Olfr1501 UTSW 19 13838861 missense probably damaging 1.00
X0026:Olfr1501 UTSW 19 13838657 missense possibly damaging 0.61
Predicted Primers PCR Primer
(F):5'- GCCCAACAGATAGGAACTTCAG -3'
(R):5'- TACGCGAACAGGTCATCTTCC -3'

Sequencing Primer
(F):5'- CTTCAGACTGATGAAGCTTTAAGTC -3'
(R):5'- GCGAACAGGTCATCTTCCTTTTTG -3'
Posted On2020-10-20