Incidental Mutation 'R1714:Or8s8'
ID 190896
Institutional Source Beutler Lab
Gene Symbol Or8s8
Ensembl Gene ENSMUSG00000032987
Gene Name olfactory receptor family 8 subfamily S member 8
Synonyms GA_x6K02T2NBG7-5275017-5274082, Olfr281, MOR160-5
MMRRC Submission 039747-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.078) question?
Stock # R1714 (G1)
Quality Score 225
Status Not validated
Chromosome 15
Chromosomal Location 98354193-98355128 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 98354614 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Tyrosine at position 141 (C141Y)
Ref Sequence ENSEMBL: ENSMUSP00000150530 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000109163] [ENSMUST00000217517]
AlphaFold Q8VET6
Predicted Effect probably damaging
Transcript: ENSMUST00000109163
AA Change: C141Y

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000104791
Gene: ENSMUSG00000032987
AA Change: C141Y

DomainStartEndE-ValueType
Pfam:7tm_4 31 306 3.8e-54 PFAM
Pfam:7TM_GPCR_Srsx 35 277 2.2e-5 PFAM
Pfam:7tm_1 41 288 2.4e-22 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000217517
AA Change: C141Y

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.7%
  • 20x: 93.5%
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: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2210408I21Rik C T 13: 77,464,479 (GRCm39) T892I possibly damaging Het
Abcb11 A C 2: 69,136,925 (GRCm39) F179V probably damaging Het
Adgrg6 G T 10: 14,315,514 (GRCm39) Q597K possibly damaging Het
Ankmy1 G T 1: 92,812,916 (GRCm39) Y464* probably null Het
Apba1 G A 19: 23,922,316 (GRCm39) E795K possibly damaging Het
Aqp12 T A 1: 92,934,681 (GRCm39) V186D possibly damaging Het
Brd8 A T 18: 34,742,886 (GRCm39) S253R probably damaging Het
Cdc42se2 A T 11: 54,631,112 (GRCm39) S2R possibly damaging Het
Chd9 A C 8: 91,760,853 (GRCm39) probably benign Het
Clk4 C T 11: 51,171,245 (GRCm39) H219Y probably damaging Het
Cngb1 A G 8: 95,984,559 (GRCm39) Y417H probably damaging Het
Cr2 A T 1: 194,833,994 (GRCm39) F932I possibly damaging Het
Cxxc1 C A 18: 74,352,934 (GRCm39) R415S probably damaging Het
Dclk2 G A 3: 86,813,400 (GRCm39) A182V probably benign Het
Ddx11 T G 17: 66,455,754 (GRCm39) W718G probably damaging Het
Dmd A C X: 83,008,356 (GRCm39) T2069P probably benign Het
Dnai1 T C 4: 41,632,164 (GRCm39) F533L probably benign Het
Dnajc5b A T 3: 19,633,265 (GRCm39) R163* probably null Het
Dynll2 T A 11: 87,874,838 (GRCm39) probably null Het
Ercc5 A G 1: 44,206,499 (GRCm39) T471A probably benign Het
Fan1 T C 7: 64,016,435 (GRCm39) D563G probably benign Het
Fbxo34 A G 14: 47,766,658 (GRCm39) Y6C probably damaging Het
Fcrl5 T A 3: 87,353,713 (GRCm39) S353T probably damaging Het
Gabrb3 A T 7: 57,415,176 (GRCm39) Y82F probably damaging Het
Gm20939 C A 17: 95,183,234 (GRCm39) P157T probably damaging Het
H2bc1 T C 13: 24,117,935 (GRCm39) T69A probably benign Het
Haus3 A T 5: 34,321,041 (GRCm39) H468Q probably benign Het
Il20ra T C 10: 19,631,576 (GRCm39) V259A probably damaging Het
Isg15 A T 4: 156,284,414 (GRCm39) V38E probably damaging Het
Kcnq3 A G 15: 65,871,912 (GRCm39) S586P probably benign Het
Kl A T 5: 150,876,798 (GRCm39) Y206F probably benign Het
Klk1b24 C A 7: 43,840,939 (GRCm39) D122E probably damaging Het
Kmt2d A C 15: 98,760,831 (GRCm39) S840A unknown Het
Krt34 A G 11: 99,930,953 (GRCm39) S150P possibly damaging Het
Lamc3 A G 2: 31,830,769 (GRCm39) K1502R probably benign Het
Letm1 G T 5: 33,918,228 (GRCm39) R306S possibly damaging Het
Lnx1 C T 5: 74,768,398 (GRCm39) G397S probably null Het
Lrrc8c A G 5: 105,755,157 (GRCm39) T311A possibly damaging Het
Mpeg1 A T 19: 12,440,198 (GRCm39) D552V probably damaging Het
Myh11 C T 16: 14,054,232 (GRCm39) probably null Het
Ndufa9 T C 6: 126,799,154 (GRCm39) probably null Het
Or4e5 A C 14: 52,727,871 (GRCm39) probably null Het
Or4f4b A T 2: 111,314,008 (GRCm39) I78F probably damaging Het
Polr3d A C 14: 70,678,755 (GRCm39) M117R possibly damaging Het
Ppp5c T C 7: 16,742,628 (GRCm39) I237V probably benign Het
Prrc2c G A 1: 162,504,945 (GRCm39) T2632M probably damaging Het
Ptprg C A 14: 12,213,697 (GRCm38) Q1022K probably damaging Het
Pus10 T A 11: 23,675,542 (GRCm39) H471Q probably damaging Het
Ralgapa1 A G 12: 55,689,174 (GRCm39) V1928A probably damaging Het
Rbpms2 CACT CACTACT 9: 65,558,947 (GRCm39) probably benign Het
Rbpms2 ACTGCTGCTGCTGCTGC ACTGCTGCTGCTGCTGCTGC 9: 65,558,948 (GRCm39) probably benign Het
Rfpl4 T G 7: 5,113,357 (GRCm39) T269P probably benign Het
Rgs10 A G 7: 128,004,946 (GRCm39) V72A probably damaging Het
Rsph1 T C 17: 31,474,190 (GRCm39) N289S probably benign Het
Sbk2 T C 7: 4,966,121 (GRCm39) D21G probably benign Het
Shbg A T 11: 69,507,983 (GRCm39) D127E possibly damaging Het
Spag16 A G 1: 69,882,164 (GRCm39) E52G probably damaging Het
Ssh2 G A 11: 77,344,850 (GRCm39) G945D possibly damaging Het
Sstr3 A T 15: 78,424,473 (GRCm39) D91E probably damaging Het
Syne2 C A 12: 76,101,713 (GRCm39) A669E probably benign Het
Traf3 A G 12: 111,208,907 (GRCm39) I109V probably benign Het
Ube2j1 A G 4: 33,049,886 (GRCm39) T295A probably damaging Het
Usp46 A G 5: 74,163,828 (GRCm39) V276A probably benign Het
Vmn1r200 T C 13: 22,579,640 (GRCm39) S139P possibly damaging Het
Ydjc G A 16: 16,965,663 (GRCm39) V143M probably damaging Het
Zfp169 T C 13: 48,652,330 (GRCm39) E29G probably benign Het
Zfp292 A G 4: 34,808,935 (GRCm39) S1370P probably damaging Het
Zfp763 C T 17: 33,238,591 (GRCm39) D185N probably damaging Het
Zfp827 A T 8: 79,787,202 (GRCm39) N123Y probably damaging Het
Zfp979 A T 4: 147,698,442 (GRCm39) I89N probably damaging Het
Zfr2 T C 10: 81,080,583 (GRCm39) L419P probably damaging Het
Other mutations in Or8s8
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00094:Or8s8 APN 15 98,354,299 (GRCm39) missense possibly damaging 0.61
IGL01016:Or8s8 APN 15 98,354,186 (GRCm39) utr 5 prime probably benign
IGL02372:Or8s8 APN 15 98,354,709 (GRCm39) missense probably damaging 1.00
IGL02730:Or8s8 APN 15 98,354,317 (GRCm39) missense probably damaging 1.00
R0732:Or8s8 UTSW 15 98,354,959 (GRCm39) missense possibly damaging 0.94
R1959:Or8s8 UTSW 15 98,354,634 (GRCm39) missense probably damaging 1.00
R4169:Or8s8 UTSW 15 98,354,878 (GRCm39) missense probably benign 0.00
R4902:Or8s8 UTSW 15 98,354,796 (GRCm39) missense probably damaging 0.99
R5014:Or8s8 UTSW 15 98,354,857 (GRCm39) missense possibly damaging 0.80
R6082:Or8s8 UTSW 15 98,354,647 (GRCm39) missense probably damaging 0.97
R6378:Or8s8 UTSW 15 98,354,425 (GRCm39) missense probably benign 0.42
R7383:Or8s8 UTSW 15 98,354,578 (GRCm39) missense probably damaging 1.00
R7850:Or8s8 UTSW 15 98,354,949 (GRCm39) missense probably damaging 1.00
R7853:Or8s8 UTSW 15 98,354,866 (GRCm39) missense probably benign 0.42
R7912:Or8s8 UTSW 15 98,354,574 (GRCm39) missense probably benign 0.00
R8750:Or8s8 UTSW 15 98,354,929 (GRCm39) missense probably damaging 0.97
R9326:Or8s8 UTSW 15 98,354,935 (GRCm39) missense probably damaging 1.00
R9786:Or8s8 UTSW 15 98,354,713 (GRCm39) missense possibly damaging 0.94
Predicted Primers PCR Primer
(F):5'- CTGAAGGACCTGCTGTCTGCTAAG -3'
(R):5'- TGCTCAGCACGGTGGATACAATG -3'

Sequencing Primer
(F):5'- CTGTCTGCTAAGAAAACCATCTCTG -3'
(R):5'- GCAGATCAAGATGTCCACGTTG -3'
Posted On 2014-05-14