Incidental Mutation 'R0577:Or9i16'
ID 56281
Institutional Source Beutler Lab
Gene Symbol Or9i16
Ensembl Gene ENSMUSG00000059105
Gene Name olfactory receptor family 9 subfamily I member 16
Synonyms GA_x6K02T2RE5P-4223635-4222688, Olfr1504, MOR212-2
MMRRC Submission 038767-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.088) question?
Stock # R0577 (G1)
Quality Score 197
Status Validated
Chromosome 19
Chromosomal Location 13864625-13865572 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 13865167 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 136 (T136A)
Ref Sequence ENSEMBL: ENSMUSP00000146610 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000078282] [ENSMUST00000209192]
AlphaFold Q8VFQ4
Predicted Effect probably damaging
Transcript: ENSMUST00000078282
AA Change: T136A

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000077400
Gene: ENSMUSG00000059105
AA Change: T136A

DomainStartEndE-ValueType
Pfam:7tm_4 30 307 4.3e-46 PFAM
Pfam:7tm_1 40 313 1.5e-19 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000209192
AA Change: T136A

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.9%
  • 10x: 97.5%
  • 20x: 95.2%
Validation Efficiency 97% (30/31)
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: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aars1 T A 8: 111,769,910 (GRCm39) H336Q probably benign Het
Abcc2 A T 19: 43,807,840 (GRCm39) D827V probably damaging Het
Asph G T 4: 9,604,620 (GRCm39) A139E probably benign Het
Bag3 T C 7: 128,125,611 (GRCm39) M10T probably benign Het
Bod1l T C 5: 41,952,230 (GRCm39) D2894G probably damaging Het
Cdk12 T C 11: 98,094,332 (GRCm39) S47P probably damaging Het
Dchs1 C T 7: 105,413,462 (GRCm39) V1118I possibly damaging Het
Ddi2 A T 4: 141,411,818 (GRCm39) C365S possibly damaging Het
Eef1g A G 19: 8,950,406 (GRCm39) D264G probably benign Het
Fbxw17 T C 13: 50,585,619 (GRCm39) L274P probably benign Het
Gpc6 A G 14: 117,673,420 (GRCm39) T226A probably benign Het
Klf12 T A 14: 100,260,585 (GRCm39) Y48F probably damaging Het
Klhdc4 C T 8: 122,548,090 (GRCm39) A67T probably damaging Het
Macir C T 1: 97,589,551 (GRCm39) probably null Het
Madd C T 2: 90,968,740 (GRCm39) E1596K possibly damaging Het
Mov10l1 A G 15: 88,889,930 (GRCm39) Y533C probably damaging Het
Mtif2 G T 11: 29,490,862 (GRCm39) probably null Het
Mtmr6 G A 14: 60,534,087 (GRCm39) V442I possibly damaging Het
Or4k15b C T 14: 50,272,249 (GRCm39) G204R probably damaging Het
Or5ac23 A T 16: 59,149,061 (GRCm39) D270E probably benign Het
Pdcd11 A G 19: 47,087,271 (GRCm39) N277S probably benign Het
Pias2 A T 18: 77,184,977 (GRCm39) L12F probably damaging Het
Potefam1 G T 2: 111,024,694 (GRCm39) Q57K probably benign Het
Rnf213 G T 11: 119,334,106 (GRCm39) R3105L probably damaging Het
Rps11 A G 7: 44,772,274 (GRCm39) V111A probably benign Het
Rrs1 C A 1: 9,616,026 (GRCm39) probably null Het
Thsd7a T C 6: 12,321,047 (GRCm39) T1543A possibly damaging Het
Vmn2r86 C A 10: 130,288,444 (GRCm39) R352S probably benign Het
Zfp141 T C 7: 42,125,938 (GRCm39) N178S probably benign Het
Zfp955a A T 17: 33,461,068 (GRCm39) F355I probably damaging Het
Other mutations in Or9i16
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00332:Or9i16 APN 19 13,864,945 (GRCm39) missense probably benign
IGL00885:Or9i16 APN 19 13,865,532 (GRCm39) missense probably benign 0.17
IGL01084:Or9i16 APN 19 13,864,866 (GRCm39) missense probably damaging 1.00
IGL01522:Or9i16 APN 19 13,864,722 (GRCm39) nonsense probably null
IGL01727:Or9i16 APN 19 13,865,242 (GRCm39) missense probably damaging 0.98
IGL02440:Or9i16 APN 19 13,865,223 (GRCm39) missense probably damaging 1.00
IGL03342:Or9i16 APN 19 13,864,801 (GRCm39) missense probably damaging 1.00
R0531:Or9i16 UTSW 19 13,865,116 (GRCm39) missense possibly damaging 0.62
R1028:Or9i16 UTSW 19 13,865,159 (GRCm39) missense probably damaging 0.97
R1674:Or9i16 UTSW 19 13,864,954 (GRCm39) missense probably benign 0.01
R3906:Or9i16 UTSW 19 13,865,070 (GRCm39) missense probably damaging 1.00
R4598:Or9i16 UTSW 19 13,865,381 (GRCm39) missense probably damaging 1.00
R4658:Or9i16 UTSW 19 13,864,912 (GRCm39) missense probably benign 0.19
R4676:Or9i16 UTSW 19 13,864,765 (GRCm39) missense probably damaging 1.00
R5919:Or9i16 UTSW 19 13,865,209 (GRCm39) missense probably damaging 1.00
R5943:Or9i16 UTSW 19 13,865,116 (GRCm39) missense possibly damaging 0.62
R8112:Or9i16 UTSW 19 13,864,753 (GRCm39) missense probably damaging 1.00
R9616:Or9i16 UTSW 19 13,864,861 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CTTGGTCTCACTACAGGCAAGCTTC -3'
(R):5'- TAATTCAGAGTGACCCTCGGCTCC -3'

Sequencing Primer
(F):5'- TACAGGCAAGCTTCATCAGG -3'
(R):5'- CATCTGTTATTGTGCCACAGC -3'
Posted On 2013-07-11