Incidental Mutation 'R0682:Or9i14'
ID 61032
Institutional Source Beutler Lab
Gene Symbol Or9i14
Ensembl Gene ENSMUSG00000045395
Gene Name olfactory receptor family 9 subfamily I member 14
Synonyms GA_x6K02T2RE5P-4147744-4146800, Olfr1499, MOR211-2
MMRRC Submission 038867-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.280) question?
Stock # R0682 (G1)
Quality Score 156
Status Not validated
Chromosome 19
Chromosomal Location 13792008-13792952 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 13792501 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Tyrosine at position 151 (C151Y)
Ref Sequence ENSEMBL: ENSMUSP00000150330 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055672] [ENSMUST00000216659]
AlphaFold Q8VG65
Predicted Effect possibly damaging
Transcript: ENSMUST00000055672
AA Change: C151Y

PolyPhen 2 Score 0.944 (Sensitivity: 0.80; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000059747
Gene: ENSMUSG00000045395
AA Change: C151Y

DomainStartEndE-ValueType
Pfam:7tm_4 31 307 2.6e-44 PFAM
Pfam:7tm_1 41 290 1.5e-19 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000216659
AA Change: C151Y

PolyPhen 2 Score 0.944 (Sensitivity: 0.80; Specificity: 0.95)
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.8%
  • 10x: 97.6%
  • 20x: 95.5%
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: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700001J03Rik T C 5: 146,121,650 (GRCm39) H83R probably benign Het
Abcd3 A C 3: 121,563,216 (GRCm39) I471S possibly damaging Het
Abcg1 G A 17: 31,330,225 (GRCm39) V509I probably benign Het
Adamts9 A T 6: 92,880,783 (GRCm39) N497K possibly damaging Het
Agap2 A G 10: 126,919,351 (GRCm39) S479G unknown Het
Asic2 T C 11: 80,777,506 (GRCm39) I402V possibly damaging Het
Atp1a2 G A 1: 172,112,164 (GRCm39) T577I probably benign Het
Atraid T A 5: 31,209,612 (GRCm39) I92K probably damaging Het
Dpp10 C A 1: 123,832,852 (GRCm39) A31S probably damaging Het
Erich6 A T 3: 58,544,232 (GRCm39) F118L probably benign Het
Galnt18 T C 7: 111,119,222 (GRCm39) Y418C probably damaging Het
Herc1 T A 9: 66,389,263 (GRCm39) C3927S possibly damaging Het
Ifit2 G A 19: 34,551,012 (GRCm39) R184H probably benign Het
Kif24 A T 4: 41,428,620 (GRCm39) N113K probably benign Het
Lrp1b T A 2: 41,185,653 (GRCm39) Y1354F probably benign Het
Muc1 T A 3: 89,138,439 (GRCm39) I427N probably damaging Het
Muc5ac A G 7: 141,359,406 (GRCm39) T1288A possibly damaging Het
Or7g32 C A 9: 19,388,645 (GRCm39) M300I probably benign Het
Pex26 T A 6: 121,161,363 (GRCm39) V47E probably damaging Het
Plekhm2 T C 4: 141,355,436 (GRCm39) I871V probably damaging Het
Rasal2 A G 1: 157,006,779 (GRCm39) S111P probably damaging Het
Rnf133 A T 6: 23,649,569 (GRCm39) I163N probably damaging Het
Rrp8 A C 7: 105,383,218 (GRCm39) D349E probably damaging Het
Sdhd G T 9: 50,511,905 (GRCm39) Q38K probably benign Het
Ssh1 C T 5: 114,098,718 (GRCm39) S117N probably damaging Het
Tbc1d2b A G 9: 90,131,915 (GRCm39) M148T probably benign Het
Tnni3k A G 3: 154,645,665 (GRCm39) S470P probably damaging Het
Tnr C T 1: 159,679,877 (GRCm39) Q284* probably null Het
Trim30a A C 7: 104,078,389 (GRCm39) V229G probably damaging Het
Trim43a G A 9: 88,464,199 (GRCm39) E37K probably benign Het
U2surp C T 9: 95,366,496 (GRCm39) V470I probably benign Het
Uck2 T C 1: 167,064,259 (GRCm39) D90G probably damaging Het
Vmn1r229 A T 17: 21,034,950 (GRCm39) E65V probably benign Het
Vmn2r26 A G 6: 124,038,129 (GRCm39) E568G probably damaging Het
Whamm A G 7: 81,235,886 (GRCm39) E363G probably damaging Het
Wrap53 A G 11: 69,453,272 (GRCm39) S390P probably damaging Het
Wrn A G 8: 33,757,848 (GRCm39) S814P probably benign Het
Zfp329 A G 7: 12,544,211 (GRCm39) C438R probably damaging Het
Zkscan8 T C 13: 21,710,930 (GRCm39) Y60C probably damaging Het
Other mutations in Or9i14
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01534:Or9i14 APN 19 13,792,666 (GRCm39) missense probably benign 0.09
IGL01844:Or9i14 APN 19 13,792,180 (GRCm39) missense possibly damaging 0.95
IGL03102:Or9i14 APN 19 13,792,735 (GRCm39) missense probably damaging 1.00
IGL03352:Or9i14 APN 19 13,792,292 (GRCm39) missense probably damaging 1.00
R0218:Or9i14 UTSW 19 13,792,342 (GRCm39) missense probably benign 0.19
R0490:Or9i14 UTSW 19 13,792,219 (GRCm39) missense probably damaging 1.00
R1301:Or9i14 UTSW 19 13,792,726 (GRCm39) missense probably damaging 1.00
R1328:Or9i14 UTSW 19 13,792,900 (GRCm39) missense probably benign 0.01
R2100:Or9i14 UTSW 19 13,792,600 (GRCm39) missense possibly damaging 0.95
R3701:Or9i14 UTSW 19 13,792,712 (GRCm39) missense probably benign 0.03
R4563:Or9i14 UTSW 19 13,792,646 (GRCm39) missense probably benign 0.01
R4709:Or9i14 UTSW 19 13,792,814 (GRCm39) missense possibly damaging 0.94
R5231:Or9i14 UTSW 19 13,792,711 (GRCm39) missense probably damaging 0.99
R5301:Or9i14 UTSW 19 13,792,933 (GRCm39) missense probably damaging 0.99
R5343:Or9i14 UTSW 19 13,792,324 (GRCm39) missense probably damaging 1.00
R6268:Or9i14 UTSW 19 13,792,671 (GRCm39) nonsense probably null
R6442:Or9i14 UTSW 19 13,792,992 (GRCm39) start gained probably benign
R7132:Or9i14 UTSW 19 13,792,786 (GRCm39) missense probably benign 0.09
R7764:Or9i14 UTSW 19 13,792,111 (GRCm39) missense probably benign 0.01
R7943:Or9i14 UTSW 19 13,792,600 (GRCm39) missense probably damaging 0.99
R8703:Or9i14 UTSW 19 13,792,105 (GRCm39) missense probably damaging 1.00
R8736:Or9i14 UTSW 19 13,792,358 (GRCm39) missense probably benign 0.05
R9069:Or9i14 UTSW 19 13,792,735 (GRCm39) missense probably damaging 1.00
R9177:Or9i14 UTSW 19 13,792,388 (GRCm39) missense probably damaging 1.00
R9258:Or9i14 UTSW 19 13,792,099 (GRCm39) nonsense probably null
R9268:Or9i14 UTSW 19 13,792,388 (GRCm39) missense probably damaging 1.00
Z1088:Or9i14 UTSW 19 13,792,912 (GRCm39) missense probably damaging 1.00
Z1177:Or9i14 UTSW 19 13,792,408 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GAGAAGGTTTTACCTCTGCCACCTG -3'
(R):5'- TGTGTTGGATGCCTGCTACACC -3'

Sequencing Primer
(F):5'- CCTCATGACTGTCTTGATGATAAGC -3'
(R):5'- ATGCCTGCTACACCAGTGTC -3'
Posted On 2013-07-30