Incidental Mutation 'IGL02604:Olfr1502'
ID300173
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Olfr1502
Ensembl Gene ENSMUSG00000056858
Gene Nameolfactory receptor 1502
SynonymsGA_x6K02T2RE5P-4193992-4194942, MOR211-1
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.106) question?
Stock #IGL02604
Quality Score
Status
Chromosome19
Chromosomal Location13861795-13862745 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 13861806 bp
ZygosityHeterozygous
Amino Acid Change Asparagine to Lysine at position 4 (N4K)
Ref Sequence ENSEMBL: ENSMUSP00000073843 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000074221]
Predicted Effect probably benign
Transcript: ENSMUST00000074221
AA Change: N4K

PolyPhen 2 Score 0.006 (Sensitivity: 0.97; Specificity: 0.75)
SMART Domains Protein: ENSMUSP00000073843
Gene: ENSMUSG00000056858
AA Change: N4K

DomainStartEndE-ValueType
Pfam:7tm_4 31 307 7.1e-43 PFAM
Pfam:7tm_1 41 290 1.6e-17 PFAM
Coding Region Coverage
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: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2300002M23Rik T C 17: 35,567,948 V61A probably benign Het
Arfgef1 G A 1: 10,181,050 probably benign Het
Arhgef4 T A 1: 34,811,723 L594* probably null Het
Cacna2d3 T C 14: 29,293,109 T375A possibly damaging Het
Calb2 A C 8: 110,148,528 Y155D probably damaging Het
Camkmt A G 17: 85,096,625 T92A possibly damaging Het
Chsy3 A G 18: 59,409,115 S442G probably benign Het
Cyp4f13 T C 17: 32,932,421 I173V probably benign Het
Dapk1 A G 13: 60,748,320 T741A probably benign Het
Dennd3 T C 15: 73,556,403 I866T probably damaging Het
Dhrs2 A T 14: 55,237,321 I138F possibly damaging Het
Dscaml1 C T 9: 45,744,328 probably benign Het
Fsbp A G 4: 11,584,147 E282G probably damaging Het
Hpgds A T 6: 65,123,610 L128Q probably damaging Het
Hspa9 A G 18: 34,954,213 V13A unknown Het
Itgb3 A G 11: 104,662,443 E709G probably damaging Het
Jarid2 T C 13: 44,874,401 S148P probably damaging Het
Kcna6 C T 6: 126,739,204 G241R probably benign Het
Kdm5a T A 6: 120,431,980 N1541K probably benign Het
Kel C A 6: 41,687,582 E640D probably damaging Het
Lcp1 A T 14: 75,224,126 I520F probably benign Het
Lgr4 A G 2: 110,011,313 I524V probably damaging Het
Maats1 A G 16: 38,321,559 probably benign Het
Mup20 A C 4: 62,051,904 Y139D probably damaging Het
Notch4 T C 17: 34,565,388 probably null Het
Obox7 A G 7: 14,665,368 E173G probably benign Het
Olfr153 A T 2: 87,532,605 T191S probably damaging Het
Olfr447 T A 6: 42,912,058 C178* probably null Het
Olfr517 T A 7: 108,868,650 Y168F probably benign Het
Olfr889 C T 9: 38,115,852 Q19* probably null Het
Patl2 T G 2: 122,125,333 T241P possibly damaging Het
Pip5k1c C A 10: 81,317,321 probably null Het
Plekhg6 T C 6: 125,377,379 probably benign Het
Pon1 C A 6: 5,168,375 G344V probably damaging Het
Ppp1r21 G T 17: 88,572,743 K529N probably benign Het
Prdm15 A G 16: 97,821,942 S203P probably benign Het
Psmc2 T A 5: 21,795,100 probably null Het
Ptn T C 6: 36,715,718 M166V unknown Het
Ptpn13 A G 5: 103,501,903 N391D probably benign Het
Rnf214 A G 9: 45,869,543 S383P probably damaging Het
Rufy4 T A 1: 74,134,189 L438H probably damaging Het
Scarf2 A G 16: 17,803,744 T353A probably damaging Het
Serpinb9e A C 13: 33,257,759 I225L probably benign Het
Slc25a40 T C 5: 8,453,219 V312A probably benign Het
Tmc3 A G 7: 83,622,619 Y993C possibly damaging Het
Trim56 A C 5: 137,113,076 C529G probably damaging Het
Trim8 T C 19: 46,515,478 S490P probably damaging Het
Trmt6 A T 2: 132,810,437 Y147* probably null Het
Vmn2r109 T A 17: 20,540,701 H798L probably damaging Het
Vps35 A G 8: 85,286,389 L153P probably damaging Het
Wdr82 T C 9: 106,183,681 I131T probably damaging Het
Zfp69 A T 4: 120,931,463 D218E probably benign Het
Other mutations in Olfr1502
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00094:Olfr1502 APN 19 13861786 unclassified probably benign
IGL01061:Olfr1502 APN 19 13862705 missense possibly damaging 0.94
IGL01534:Olfr1502 APN 19 13861919 missense probably damaging 1.00
IGL02017:Olfr1502 APN 19 13862231 missense possibly damaging 0.58
IGL02039:Olfr1502 APN 19 13862719 nonsense probably null
IGL02173:Olfr1502 APN 19 13862014 missense probably benign 0.00
IGL02219:Olfr1502 APN 19 13861823 missense probably damaging 1.00
IGL02475:Olfr1502 APN 19 13862299 missense probably damaging 1.00
R0012:Olfr1502 UTSW 19 13861823 missense probably damaging 0.98
R0594:Olfr1502 UTSW 19 13862279 missense probably benign 0.04
R2184:Olfr1502 UTSW 19 13862035 missense probably benign 0.02
R2518:Olfr1502 UTSW 19 13862309 missense probably damaging 1.00
R5541:Olfr1502 UTSW 19 13861964 missense probably benign
R5587:Olfr1502 UTSW 19 13862576 missense probably damaging 1.00
R6211:Olfr1502 UTSW 19 13862574 missense probably benign 0.01
R6351:Olfr1502 UTSW 19 13861822 missense probably benign 0.04
R7575:Olfr1502 UTSW 19 13862017 missense probably damaging 1.00
Posted On2015-04-16