Incidental Mutation 'R9573:Or9a2'
ID 722111
Institutional Source Beutler Lab
Gene Symbol Or9a2
Ensembl Gene ENSMUSG00000045479
Gene Name olfactory receptor family 9 subfamily A member 2
Synonyms GA_x6K02T2P3E9-5780974-5781915, Olfr459, MOR120-1
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.200) question?
Stock # R9573 (G1)
Quality Score 225.009
Status Not validated
Chromosome 6
Chromosomal Location 41748287-41749231 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 41748940 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Leucine at position 98 (I98L)
Ref Sequence ENSEMBL: ENSMUSP00000149928 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000050412] [ENSMUST00000214752] [ENSMUST00000214976]
AlphaFold Q924H8
Predicted Effect probably benign
Transcript: ENSMUST00000050412
AA Change: I98L

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000061622
Gene: ENSMUSG00000045479
AA Change: I98L

DomainStartEndE-ValueType
Pfam:7tm_4 30 307 7.9e-46 PFAM
Pfam:7TM_GPCR_Srsx 34 304 1.7e-6 PFAM
Pfam:7tm_1 40 290 6.2e-24 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000214752
AA Change: I98L

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
Predicted Effect probably benign
Transcript: ENSMUST00000214976
AA Change: I98L

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.9%
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: 67 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Afdn T A 17: 14,050,229 (GRCm39) V472E probably damaging Het
Ak3 T C 19: 29,003,667 (GRCm39) I170V probably benign Het
Ank3 T A 10: 69,791,977 (GRCm39) L1058* probably null Het
Ankrd60 A G 2: 173,410,791 (GRCm39) V243A possibly damaging Het
Apol11b C T 15: 77,524,771 (GRCm39) E5K possibly damaging Het
Arid3c T G 4: 41,726,003 (GRCm39) E200A probably benign Het
Astn2 T G 4: 65,566,591 (GRCm39) I856L probably benign Het
Bcs1l C A 1: 74,629,492 (GRCm39) R177S probably damaging Het
Bin2 A T 15: 100,560,433 (GRCm39) F43I probably damaging Het
Braf A G 6: 39,600,544 (GRCm39) L691P probably damaging Het
Bud23 C T 5: 135,082,274 (GRCm39) V266I possibly damaging Het
Casp12 A T 9: 5,354,629 (GRCm39) I333L probably benign Het
Cavin2 T A 1: 51,328,795 (GRCm39) I84N probably damaging Het
Ccdc168 A C 1: 44,095,307 (GRCm39) Y1930* probably null Het
Ccdc196 A T 12: 78,244,098 (GRCm39) N17I Het
Cep170b T A 12: 112,691,154 (GRCm39) F24I probably damaging Het
Chd9 A G 8: 91,704,302 (GRCm39) Y719C unknown Het
Commd7 A G 2: 153,463,981 (GRCm39) M137T probably damaging Het
Dmbt1 G A 7: 130,657,910 (GRCm39) probably null Het
Dnah12 A C 14: 26,414,619 (GRCm39) T7P probably benign Het
Elapor1 A T 3: 108,373,094 (GRCm39) I548N probably damaging Het
Endod1 A T 9: 14,292,247 (GRCm39) L7Q probably damaging Het
Galnt14 C T 17: 73,802,662 (GRCm39) V477M probably damaging Het
Glis2 C T 16: 4,429,505 (GRCm39) R211C probably damaging Het
Gm4744 A T 6: 40,925,497 (GRCm39) V122D Het
Gm4952 G A 19: 12,604,090 (GRCm39) M167I probably benign Het
Hyal4 T C 6: 24,756,508 (GRCm39) V242A possibly damaging Het
Ift122 T G 6: 115,857,646 (GRCm39) S131A probably benign Het
Il4ra T A 7: 125,169,158 (GRCm39) S137T possibly damaging Het
Lcor T A 19: 41,573,471 (GRCm39) L742Q probably damaging Het
Lpin2 A G 17: 71,538,185 (GRCm39) K315R probably benign Het
Map3k6 T C 4: 132,979,774 (GRCm39) Y1258H probably damaging Het
Mapk9 A T 11: 49,769,239 (GRCm39) K290N probably damaging Het
Mfhas1 C T 8: 36,143,903 (GRCm39) H1045Y possibly damaging Het
Ndufaf7 C A 17: 79,246,036 (GRCm39) Q90K probably damaging Het
Nlrc3 A T 16: 3,771,841 (GRCm39) V157E probably benign Het
Npas4 A G 19: 5,035,837 (GRCm39) F776L probably benign Het
Nuggc A C 14: 65,848,603 (GRCm39) D184A probably benign Het
Ogdhl A G 14: 32,066,678 (GRCm39) E795G probably damaging Het
Or5a1 A G 19: 12,097,509 (GRCm39) I189T probably damaging Het
Pcbp1 A T 6: 86,502,677 (GRCm39) M74K possibly damaging Het
Plk4 A G 3: 40,763,257 (GRCm39) D476G probably benign Het
Prox2 G A 12: 85,141,766 (GRCm39) Q146* probably null Het
Rab44 A T 17: 29,364,277 (GRCm39) Y617F unknown Het
Rabepk T C 2: 34,675,627 (GRCm39) R168G probably benign Het
Rbmyf9 T A Y: 3,775,370 (GRCm39) M40K possibly damaging Het
Rif1 T G 2: 52,000,466 (GRCm39) S1307A probably benign Het
Ror2 C T 13: 53,265,467 (GRCm39) V542I probably benign Het
Rtp1 A G 16: 23,250,159 (GRCm39) I175V possibly damaging Het
Slc11a2 T A 15: 100,304,225 (GRCm39) I158F probably damaging Het
Slc24a3 T G 2: 145,455,548 (GRCm39) M479R probably damaging Het
Slc4a9 T C 18: 36,668,589 (GRCm39) F723S probably damaging Het
Syne2 C A 12: 75,927,134 (GRCm39) N93K probably damaging Het
Sytl2 A G 7: 90,057,599 (GRCm39) Q846R probably damaging Het
Tas2r116 A C 6: 132,833,140 (GRCm39) H247P probably benign Het
Tcstv3 T C 13: 120,779,130 (GRCm39) S10P probably damaging Het
Tgm7 T C 2: 120,934,606 (GRCm39) N124S probably benign Het
Tmem219 A T 7: 126,490,933 (GRCm39) Y175N probably damaging Het
Tnfrsf18 G A 4: 156,112,484 (GRCm39) G114S possibly damaging Het
Trim38 G A 13: 23,966,688 (GRCm39) C45Y probably benign Het
Tshz1 T C 18: 84,032,404 (GRCm39) E668G probably benign Het
Ubr4 T A 4: 139,148,450 (GRCm39) M382K Het
Vps39 T C 2: 120,155,179 (GRCm39) E549G possibly damaging Het
Wdr35 G A 12: 9,078,014 (GRCm39) G1135D probably benign Het
Zbtb46 A G 2: 181,053,548 (GRCm39) L388P probably benign Het
Zdhhc25 T A 15: 88,485,307 (GRCm39) M214K probably damaging Het
Zfp735 G A 11: 73,602,936 (GRCm39) E627K possibly damaging Het
Other mutations in Or9a2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00896:Or9a2 APN 6 41,749,047 (GRCm39) missense probably damaging 1.00
IGL01460:Or9a2 APN 6 41,749,216 (GRCm39) missense probably benign 0.12
IGL02465:Or9a2 APN 6 41,748,490 (GRCm39) missense probably damaging 1.00
R0352:Or9a2 UTSW 6 41,749,058 (GRCm39) missense probably damaging 0.99
R0443:Or9a2 UTSW 6 41,748,829 (GRCm39) missense possibly damaging 0.75
R0480:Or9a2 UTSW 6 41,749,198 (GRCm39) missense probably benign 0.01
R1491:Or9a2 UTSW 6 41,748,456 (GRCm39) missense possibly damaging 0.95
R1495:Or9a2 UTSW 6 41,748,837 (GRCm39) missense probably damaging 1.00
R2103:Or9a2 UTSW 6 41,748,939 (GRCm39) missense probably benign 0.36
R3688:Or9a2 UTSW 6 41,749,160 (GRCm39) nonsense probably null
R3910:Or9a2 UTSW 6 41,749,083 (GRCm39) missense probably benign 0.00
R4709:Or9a2 UTSW 6 41,748,442 (GRCm39) missense probably benign 0.06
R4710:Or9a2 UTSW 6 41,748,442 (GRCm39) missense probably benign 0.06
R4960:Or9a2 UTSW 6 41,749,003 (GRCm39) missense probably damaging 0.97
R5162:Or9a2 UTSW 6 41,748,706 (GRCm39) missense possibly damaging 0.80
R5236:Or9a2 UTSW 6 41,749,045 (GRCm39) missense probably benign 0.00
R5441:Or9a2 UTSW 6 41,748,782 (GRCm39) missense probably benign 0.00
R7171:Or9a2 UTSW 6 41,748,961 (GRCm39) missense probably benign 0.09
R7400:Or9a2 UTSW 6 41,748,678 (GRCm39) missense probably damaging 1.00
R8115:Or9a2 UTSW 6 41,748,472 (GRCm39) missense probably benign 0.00
R8346:Or9a2 UTSW 6 41,749,057 (GRCm39) missense probably damaging 1.00
R8363:Or9a2 UTSW 6 41,748,684 (GRCm39) missense probably benign 0.06
R9700:Or9a2 UTSW 6 41,749,076 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TGGCCAGATTTCAGAAAGGAACC -3'
(R):5'- TTTCCCTGGATCCCAAGAGC -3'

Sequencing Primer
(F):5'- GATTTCAGAAAGGAACCCAAACATC -3'
(R):5'- CTATTCAGTGACACTGCTGGGAAAC -3'
Posted On 2022-08-09