Incidental Mutation 'R7040:Olfr1508'
ID 547013
Institutional Source Beutler Lab
Gene Symbol Olfr1508
Ensembl Gene ENSMUSG00000057564
Gene Name olfactory receptor 1508
Synonyms MOR244-4, GA_x6K02T2RJGY-520647-521579, MOR244-2, MOR10
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.054) question?
Stock # R7040 (G1)
Quality Score 225.009
Status Not validated
Chromosome 14
Chromosomal Location 52458829-52467495 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) T to C at 52463475 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 178 (D178G)
Ref Sequence ENSEMBL: ENSMUSP00000145649 (fasta)
AlphaFold Q9R0K4
Predicted Effect probably benign
Transcript: ENSMUST00000205811
Predicted Effect possibly damaging
Transcript: ENSMUST00000206520
AA Change: D178G

PolyPhen 2 Score 0.879 (Sensitivity: 0.82; Specificity: 0.94)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.9%
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: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9130023H24Rik A G 7: 128,236,725 L232P possibly damaging Het
Acaa1a T C 9: 119,349,038 V312A probably damaging Het
Bmp2 A G 2: 133,561,684 D385G probably damaging Het
C1qtnf9 T C 14: 60,779,792 V257A probably damaging Het
Cd3d G A 9: 44,985,693 V122I probably damaging Het
Cdc37 T C 9: 21,142,223 E199G probably damaging Het
Crb2 T A 2: 37,787,684 D326E probably benign Het
Cyp2c29 A C 19: 39,330,337 K420N possibly damaging Het
Cyp2g1 A C 7: 26,820,759 D472A probably damaging Het
Dab2 A C 15: 6,422,251 H116P probably damaging Het
Dnah7b G C 1: 46,236,809 E2619Q probably benign Het
Dsg4 A T 18: 20,451,852 M208L probably benign Het
Eif4enif1 T G 11: 3,234,040 V521G probably benign Het
Fan1 T A 7: 64,372,486 N340Y probably damaging Het
Fpr-rs6 A G 17: 20,182,934 M55T probably damaging Het
Grhpr A G 4: 44,985,362 S101G probably damaging Het
Kif15 T A 9: 123,011,614 D33E possibly damaging Het
Krt1 AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC 15: 101,850,378 probably benign Het
Lama4 A G 10: 39,060,162 Q611R possibly damaging Het
Lrrc47 T A 4: 154,020,452 *123R probably null Het
Map4k3 A C 17: 80,680,915 V36G probably damaging Het
Mme T A 3: 63,368,923 I707N probably damaging Het
Muc2 A G 7: 141,751,457 E166G unknown Het
Mucl1 T A 15: 103,753,578 T108S possibly damaging Het
Myo1h A T 5: 114,359,744 D53V possibly damaging Het
Naa15 T A 3: 51,472,784 L811Q possibly damaging Het
Nalcn T C 14: 123,287,855 T1487A probably benign Het
Nme8 A T 13: 19,694,328 L87H probably damaging Het
Nr2e1 A G 10: 42,568,378 V245A probably damaging Het
Nt5c2 A T 19: 46,893,535 F291Y possibly damaging Het
Olfr1337 T C 4: 118,781,986 M200V probably benign Het
Olfr556 A T 7: 102,670,730 Q270L probably benign Het
Olfr668 A T 7: 104,925,510 C85S probably benign Het
Ooep T C 9: 78,378,401 N43S possibly damaging Het
Ovch2 A T 7: 107,796,565 I82N probably damaging Het
Palb2 A T 7: 122,114,399 M524K possibly damaging Het
Patj T C 4: 98,441,080 S524P probably benign Het
Patl1 T A 19: 11,929,954 Y401N possibly damaging Het
Pcdhb20 A T 18: 37,504,717 T99S probably benign Het
Plcb4 G A 2: 135,932,262 A155T probably benign Het
Rpap3 A G 15: 97,679,112 V585A possibly damaging Het
Sorbs1 G C 19: 40,376,800 R180G probably benign Het
Spen T A 4: 141,494,382 T302S unknown Het
Tenm4 G A 7: 96,553,496 R106H probably benign Het
Ube2o T C 11: 116,541,860 E760G probably benign Het
Uimc1 T A 13: 55,075,454 probably null Het
Usp16 C T 16: 87,480,929 A689V probably damaging Het
Vmn2r60 G A 7: 42,142,242 A530T probably benign Het
Vps8 T A 16: 21,575,022 M1185K probably damaging Het
Vwa8 T C 14: 78,912,205 S136P probably damaging Het
Ythdc2 A G 18: 44,834,462 N175S probably benign Het
Zfp160 A T 17: 21,026,532 H448L probably damaging Het
Zfp90 T A 8: 106,425,009 C451* probably null Het
Zfp945 A G 17: 22,852,290 C212R probably damaging Het
Other mutations in Olfr1508
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01596:Olfr1508 APN 14 52463365 missense probably damaging 0.98
IGL02601:Olfr1508 APN 14 52463345 nonsense probably null
IGL02635:Olfr1508 APN 14 52463794 missense probably damaging 1.00
R0139:Olfr1508 UTSW 14 52463212 missense probably damaging 0.98
R0501:Olfr1508 UTSW 14 52463926 start codon destroyed possibly damaging 0.79
R0600:Olfr1508 UTSW 14 52463509 missense probably benign 0.00
R0612:Olfr1508 UTSW 14 52463551 missense probably benign 0.00
R1691:Olfr1508 UTSW 14 52463831 missense possibly damaging 0.95
R4290:Olfr1508 UTSW 14 52463985 missense probably damaging 1.00
R4837:Olfr1508 UTSW 14 52463646 missense probably damaging 1.00
R4946:Olfr1508 UTSW 14 52463283 missense probably damaging 1.00
R5073:Olfr1508 UTSW 14 52463575 missense probably damaging 1.00
R5135:Olfr1508 UTSW 14 52463854 missense probably benign 0.00
R5384:Olfr1508 UTSW 14 52463257 missense probably benign 0.41
R5663:Olfr1508 UTSW 14 52463595 missense probably benign 0.12
R5861:Olfr1508 UTSW 14 52463496 missense probably damaging 1.00
R6244:Olfr1508 UTSW 14 52463895 missense probably damaging 1.00
R7216:Olfr1508 UTSW 14 52463488 missense probably damaging 1.00
R7560:Olfr1508 UTSW 14 52463394 missense probably damaging 1.00
R8310:Olfr1508 UTSW 14 52463823 missense probably damaging 1.00
R8691:Olfr1508 UTSW 14 52463901 missense possibly damaging 0.46
R8942:Olfr1508 UTSW 14 52463235 missense probably damaging 0.98
R9185:Olfr1508 UTSW 14 52463527 missense probably benign 0.33
R9218:Olfr1508 UTSW 14 52463331 missense probably damaging 0.97
Predicted Primers PCR Primer
(F):5'- ACAGGTGGACAAGGCTTTC -3'
(R):5'- TGCCTGCACAGAGATCTTCC -3'

Sequencing Primer
(F):5'- GTGGACAAGGCTTTCCTCTTGC -3'
(R):5'- CTTACTGTCATGGCCTATGATCG -3'
Posted On 2019-05-13