Incidental Mutation 'IGL02658:Or8s16'
ID 302440
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or8s16
Ensembl Gene ENSMUSG00000062037
Gene Name olfactory receptor family 8 subfamily S member 16
Synonyms GA_x6K02T2N22H-3824-2865, MOR160-3, Olfr257, GA_x6K02T2NBG7-5440777-5441736, Olfr285
Accession Numbers
Essential gene? Probably non essential (E-score: 0.056) question?
Stock # IGL02658
Quality Score
Status
Chromosome 15
Chromosomal Location 98210470-98211429 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 98211237 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 65 (S65P)
Ref Sequence ENSEMBL: ENSMUSP00000150788 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000079736] [ENSMUST00000216901]
AlphaFold Q7TS17
Predicted Effect probably damaging
Transcript: ENSMUST00000079736
AA Change: S65P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000078672
Gene: ENSMUSG00000062037
AA Change: S65P

DomainStartEndE-ValueType
Pfam:7tm_4 29 304 9.3e-47 PFAM
Pfam:7tm_1 39 286 5.9e-19 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000216901
AA Change: S65P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
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: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca8b T A 11: 109,843,386 (GRCm39) Y946F probably benign Het
Abcb4 T G 5: 8,984,240 (GRCm39) W657G probably benign Het
Adcy1 T C 11: 7,088,279 (GRCm39) probably benign Het
Arap3 A G 18: 38,124,047 (GRCm39) V351A probably benign Het
Bpifb9b A C 2: 154,153,201 (GRCm39) Y89S probably benign Het
Carns1 C T 19: 4,223,083 (GRCm39) C47Y probably benign Het
Chd5 C T 4: 152,445,050 (GRCm39) H344Y probably damaging Het
Ctnna2 T C 6: 76,957,807 (GRCm39) T481A probably benign Het
Cyth1 T A 11: 118,073,072 (GRCm39) D264V probably damaging Het
Dph1 C A 11: 75,071,461 (GRCm39) L311F probably benign Het
Eif3l A G 15: 78,961,142 (GRCm39) D65G probably damaging Het
Gtf2a1l T A 17: 88,976,146 (GRCm39) F3Y probably benign Het
Hcn4 A T 9: 58,766,748 (GRCm39) T770S unknown Het
Hydin A T 8: 111,139,908 (GRCm39) I726F possibly damaging Het
Klf2 A G 8: 73,072,940 (GRCm39) I7V probably benign Het
Ltn1 A T 16: 87,212,662 (GRCm39) L633H probably damaging Het
Ncoa3 A G 2: 165,893,313 (GRCm39) D206G probably benign Het
Nlrp4a T G 7: 26,149,138 (GRCm39) D248E probably benign Het
Nyap1 A G 5: 137,733,746 (GRCm39) I429T probably damaging Het
Or1j10 T A 2: 36,267,072 (GRCm39) C95S probably damaging Het
Or2p2 G A 13: 21,256,982 (GRCm39) T163I probably damaging Het
Or2t6 T A 14: 14,175,732 (GRCm38) M117L possibly damaging Het
Or51g1 A G 7: 102,633,537 (GRCm39) M278T probably benign Het
Pcf11 T C 7: 92,296,254 (GRCm39) E1322G probably damaging Het
Plcxd2 A T 16: 45,792,689 (GRCm39) F217I probably benign Het
Plxna4 A T 6: 32,162,346 (GRCm39) I1389N probably damaging Het
Ppp1r15a T C 7: 45,174,091 (GRCm39) Y239C probably benign Het
Psma6 A G 12: 55,458,996 (GRCm39) E126G probably benign Het
R3hcc1l T A 19: 42,551,141 (GRCm39) V46E probably damaging Het
Rap1gds1 G T 3: 138,663,240 (GRCm39) H320N probably damaging Het
Sdhaf3 A G 6: 7,038,992 (GRCm39) M105V probably damaging Het
Slc22a26 T A 19: 7,765,613 (GRCm39) N345I probably benign Het
Sncaip T C 18: 53,028,027 (GRCm39) I412T possibly damaging Het
Sorcs1 A T 19: 50,178,530 (GRCm39) I864N probably damaging Het
Spag5 C T 11: 78,212,157 (GRCm39) Q1062* probably null Het
Srrm1 G A 4: 135,052,415 (GRCm39) P658L unknown Het
Szrd1 A G 4: 140,867,057 (GRCm39) probably benign Het
Tns2 C A 15: 102,016,231 (GRCm39) probably benign Het
Trcg1 C A 9: 57,149,511 (GRCm39) S361* probably null Het
Tshz3 T C 7: 36,468,583 (GRCm39) F191L probably damaging Het
Ttc39a T C 4: 109,280,090 (GRCm39) V124A probably damaging Het
Ttf1 T C 2: 28,964,023 (GRCm39) I633T probably damaging Het
Zfp691 A G 4: 119,027,704 (GRCm39) F176S probably damaging Het
Other mutations in Or8s16
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01986:Or8s16 APN 15 98,210,660 (GRCm39) missense probably damaging 0.99
R1423:Or8s16 UTSW 15 98,211,324 (GRCm39) missense probably damaging 0.99
R1442:Or8s16 UTSW 15 98,211,068 (GRCm39) missense probably damaging 0.98
R1863:Or8s16 UTSW 15 98,211,372 (GRCm39) missense probably benign 0.02
R1938:Or8s16 UTSW 15 98,211,261 (GRCm39) missense probably damaging 1.00
R4815:Or8s16 UTSW 15 98,210,561 (GRCm39) missense probably damaging 1.00
R5248:Or8s16 UTSW 15 98,211,311 (GRCm39) missense probably damaging 1.00
R5879:Or8s16 UTSW 15 98,211,369 (GRCm39) missense probably benign 0.00
R6000:Or8s16 UTSW 15 98,211,317 (GRCm39) missense probably benign 0.08
R6371:Or8s16 UTSW 15 98,211,219 (GRCm39) missense possibly damaging 0.46
R7466:Or8s16 UTSW 15 98,211,261 (GRCm39) missense probably damaging 1.00
R7708:Or8s16 UTSW 15 98,211,029 (GRCm39) missense probably damaging 1.00
R8261:Or8s16 UTSW 15 98,210,546 (GRCm39) missense probably benign 0.00
R8734:Or8s16 UTSW 15 98,210,954 (GRCm39) missense probably damaging 1.00
R9462:Or8s16 UTSW 15 98,211,186 (GRCm39) missense possibly damaging 0.90
Posted On 2015-04-16