Incidental Mutation 'R7076:Olfr1489'
ID549252
Institutional Source Beutler Lab
Gene Symbol Olfr1489
Ensembl Gene ENSMUSG00000045678
Gene Nameolfactory receptor 1489
SynonymsGA_x6K02T2RE5P-3965668-3966609, MOR202-19
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.052) question?
Stock #R7076 (G1)
Quality Score225.009
Status Validated
Chromosome19
Chromosomal Location13631621-13643987 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to T at 13633880 bp
ZygosityHeterozygous
Amino Acid Change Methionine to Isoleucine at position 256 (M256I)
Ref Sequence ENSEMBL: ENSMUSP00000149711 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000053113] [ENSMUST00000217182]
Predicted Effect possibly damaging
Transcript: ENSMUST00000053113
AA Change: M256I

PolyPhen 2 Score 0.948 (Sensitivity: 0.79; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000062444
Gene: ENSMUSG00000045678
AA Change: M256I

DomainStartEndE-ValueType
Pfam:7tm_4 29 306 1.7e-53 PFAM
Pfam:7tm_1 39 289 1.2e-15 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000217182
AA Change: M256I

PolyPhen 2 Score 0.948 (Sensitivity: 0.79; Specificity: 0.95)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.9%
Validation Efficiency 100% (60/60)
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: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam29 A G 8: 55,871,659 C587R probably damaging Het
Adgrg7 T C 16: 56,742,406 T523A probably damaging Het
Arrdc3 A T 13: 80,890,696 K259M probably damaging Het
Becn1 A T 11: 101,295,324 N151K probably benign Het
Cars2 C T 8: 11,529,649 E270K probably damaging Het
Ccp110 C A 7: 118,732,405 P943Q probably damaging Het
Ccser2 A G 14: 36,939,829 I466T probably benign Het
Cd164 A G 10: 41,523,197 E94G probably benign Het
Cdon C T 9: 35,504,150 T1228I probably benign Het
Cubn C A 2: 13,306,280 V3145L probably benign Het
Cubn T A 2: 13,306,281 K3144N probably benign Het
Dchs1 A G 7: 105,761,871 V1649A probably benign Het
Dgka A T 10: 128,733,583 D153E probably damaging Het
Dip2b A G 15: 100,157,972 probably null Het
Dnajc21 T C 15: 10,449,631 T435A probably benign Het
F830016B08Rik A T 18: 60,300,471 I209F probably damaging Het
Ghdc C A 11: 100,769,714 S111I possibly damaging Het
Gm19965 T C 1: 116,821,275 C229R Het
Gpm6a C T 8: 55,037,451 T54I probably damaging Het
Gpr171 G T 3: 59,098,156 A66E probably damaging Het
Grm7 A G 6: 111,358,152 D508G probably benign Het
Has1 G A 17: 17,843,806 R524C probably damaging Het
Idh2 TCCCAGG T 7: 80,098,331 probably benign Het
Ighv3-8 A T 12: 114,322,782 L7Q probably damaging Het
Ints10 A T 8: 68,796,751 R78* probably null Het
Itpr1 A G 6: 108,388,296 I903V probably benign Het
Lrp1 A G 10: 127,550,183 probably null Het
Mki67 A G 7: 135,705,629 V132A probably damaging Het
Myh4 A G 11: 67,253,173 E1123G possibly damaging Het
Neurog3 A G 10: 62,133,580 T40A probably benign Het
Nipsnap3b T A 4: 53,021,095 probably null Het
Nr4a3 G A 4: 48,055,957 V328I probably damaging Het
Olfr313 G A 11: 58,817,164 R52Q probably benign Het
Olfr487 A T 7: 108,211,998 V177D probably damaging Het
Olfr654 A T 7: 104,588,223 S140C probably damaging Het
Olfr716 T C 7: 107,148,029 F238L probably damaging Het
Olfr743 T A 14: 50,533,821 Y136* probably null Het
Osbpl5 A G 7: 143,709,840 L102P probably benign Het
Ppl C T 16: 5,100,119 R503Q probably damaging Het
Ppp2r2d T C 7: 138,876,597 M321T possibly damaging Het
Prex1 T C 2: 166,633,382 Y197C probably damaging Het
Prss32 A G 17: 23,853,921 D42G possibly damaging Het
Ralgapa1 T C 12: 55,721,576 E1210G possibly damaging Het
Sdr16c5 A G 4: 4,006,591 C234R probably damaging Het
Slc23a4 A G 6: 34,956,884 S95P probably damaging Het
Srp14 T C 2: 118,479,390 T29A probably damaging Het
Tet2 T A 3: 133,467,023 H1826L possibly damaging Het
Tfr2 A T 5: 137,583,574 Y641F probably damaging Het
Tmco5b A G 2: 113,287,421 N27D probably damaging Het
Tvp23a T C 16: 10,428,735 D62G probably benign Het
Usp12 A G 5: 146,737,752 F347S possibly damaging Het
Zfp407 A T 18: 84,558,476 L1504Q probably damaging Het
Zfp524 A G 7: 5,017,896 D141G possibly damaging Het
Zfp68 A G 5: 138,606,939 I374T possibly damaging Het
Zfp758 C T 17: 22,375,156 H208Y probably benign Het
Zfp804b T C 5: 6,769,751 H1104R probably benign Het
Znrf2 T A 6: 54,842,695 *75K probably null Het
Zzef1 T C 11: 72,899,559 V2113A probably benign Het
Other mutations in Olfr1489
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00236:Olfr1489 APN 19 13633539 missense probably benign 0.25
IGL03052:Olfr1489 UTSW 19 13633726 missense probably benign 0.00
R0179:Olfr1489 UTSW 19 13633140 missense probably damaging 1.00
R0270:Olfr1489 UTSW 19 13633684 missense probably damaging 1.00
R0633:Olfr1489 UTSW 19 13633336 missense probably damaging 0.99
R4466:Olfr1489 UTSW 19 13633437 missense probably damaging 0.97
R4884:Olfr1489 UTSW 19 13634027 missense probably benign 0.14
R5247:Olfr1489 UTSW 19 13633414 missense probably damaging 1.00
R5332:Olfr1489 UTSW 19 13633365 missense possibly damaging 0.91
R5754:Olfr1489 UTSW 19 13633993 missense probably damaging 0.99
R6165:Olfr1489 UTSW 19 13633143 missense possibly damaging 0.93
R6165:Olfr1489 UTSW 19 13633588 missense probably benign 0.02
R6221:Olfr1489 UTSW 19 13633466 nonsense probably null
R6486:Olfr1489 UTSW 19 13633691 missense probably damaging 1.00
R7008:Olfr1489 UTSW 19 13633621 missense probably damaging 1.00
R7539:Olfr1489 UTSW 19 13633569 nonsense probably null
R8278:Olfr1489 UTSW 19 13633594 missense possibly damaging 0.87
Z1088:Olfr1489 UTSW 19 13633453 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TCTTGGCAGCACTCAATATAGC -3'
(R):5'- AGGGGCTTCATCTATGAAATACC -3'

Sequencing Primer
(F):5'- GGCAGCACTCAATATAGCTTTAAC -3'
(R):5'- TCTTACACTTAGACTAATCCCAGTG -3'
Posted On2019-05-15