Incidental Mutation 'R6386:Olfr485'
Institutional Source Beutler Lab
Gene Symbol Olfr485
Ensembl Gene ENSMUSG00000108995
Gene Nameolfactory receptor 485
SynonymsGA_x6K02T2PBJ9-10489044-10488091, MOR204-30P, MOR204-40_p
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.117) question?
Stock #R6386 (G1)
Quality Score225.009
Status Not validated
Chromosomal Location108158918-108159871 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 108159202 bp
Amino Acid Change Tyrosine to Asparagine at position 224 (Y224N)
Ref Sequence ENSEMBL: ENSMUSP00000147194 (fasta)
Predicted Effect probably damaging
Transcript: ENSMUST00000208296
AA Change: Y224N

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.1%
  • 20x: 96.6%
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: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ak6 TGACGA TGA 13: 100,655,803 probably benign Het
Arap2 A T 5: 62,604,522 N1620K possibly damaging Het
Atf6b T C 17: 34,651,851 S396P probably damaging Het
Cc2d1a A G 8: 84,138,537 M469T probably damaging Het
Ceacam3 A G 7: 17,158,219 N296D probably benign Het
Cep57l1 A T 10: 41,743,132 S80T probably damaging Het
Clip4 C A 17: 71,834,194 Y514* probably null Het
Cop1 T C 1: 159,289,031 I125T probably damaging Het
Cstf1 T C 2: 172,377,896 V309A probably damaging Het
Cyp4a29 T G 4: 115,247,075 probably null Het
F830045P16Rik G A 2: 129,472,818 H180Y probably damaging Het
Foxp4 T C 17: 47,878,462 K237E unknown Het
Fstl5 A T 3: 76,322,066 H58L probably benign Het
Gje1 A G 10: 14,716,621 F139S probably damaging Het
Gpatch1 T C 7: 35,291,840 D593G probably damaging Het
Inpp5d T A 1: 87,699,675 L566Q probably damaging Het
Mtch2 A G 2: 90,849,395 T38A probably benign Het
Mvb12b A T 2: 33,827,742 I129N probably damaging Het
Npffr2 T C 5: 89,582,697 V162A probably benign Het
Olfr1424 A T 19: 12,059,556 N65K probably damaging Het
Pkhd1 G A 1: 20,551,020 R805C probably damaging Het
Ppp4r4 T C 12: 103,593,105 L406P probably damaging Het
Prl3d2 A G 13: 27,127,303 D186G probably damaging Het
Rfc5 T C 5: 117,385,398 T112A probably benign Het
Rnf148 A G 6: 23,654,484 L171P probably damaging Het
Rps24 G A 14: 24,492,048 G71S possibly damaging Het
Slco2a1 G A 9: 103,076,988 V453I probably benign Het
Spidr T C 16: 15,968,560 K440E probably benign Het
Syndig1 C A 2: 149,899,576 N27K probably damaging Het
Tmem62 C T 2: 120,999,114 T316I probably benign Het
Tpgs2 A T 18: 25,139,024 I258N possibly damaging Het
Vmn2r78 A T 7: 86,922,337 R452* probably null Het
Wasf3 A T 5: 146,453,417 I124F possibly damaging Het
Wbp11 T C 6: 136,820,525 T299A probably benign Het
Wdr25 T C 12: 109,025,065 S41P probably damaging Het
Zfp874b T C 13: 67,474,843 D116G possibly damaging Het
Other mutations in Olfr485
AlleleSourceChrCoordTypePredicted EffectPPH Score
R3115:Olfr485 UTSW 7 108159822 missense probably benign 0.00
R3116:Olfr485 UTSW 7 108159822 missense probably benign 0.00
R3978:Olfr485 UTSW 7 108159612 missense possibly damaging 0.52
R4722:Olfr485 UTSW 7 108159238 missense probably benign 0.04
R5337:Olfr485 UTSW 7 108159273 missense probably benign 0.01
R5553:Olfr485 UTSW 7 108159271 missense probably benign 0.02
R6258:Olfr485 UTSW 7 108158974 missense probably damaging 1.00
R6498:Olfr485 UTSW 7 108159432 missense probably benign 0.20
R7096:Olfr485 UTSW 7 108159641 missense probably benign
R7134:Olfr485 UTSW 7 108159676 missense probably damaging 1.00
R7187:Olfr485 UTSW 7 108159378 missense probably benign 0.00
R7226:Olfr485 UTSW 7 108158957 missense probably benign 0.00
R7799:Olfr485 UTSW 7 108159430 missense probably benign 0.00
Predicted Primers PCR Primer

Sequencing Primer
Posted On2018-05-04