Incidental Mutation 'R9778:Or10al2'
ID 733871
Institutional Source Beutler Lab
Gene Symbol Or10al2
Ensembl Gene ENSMUSG00000080990
Gene Name olfactory receptor family 10 subfamily AL member 2
Synonyms GA_x6K02T2PSCP-2131124-2132089, MOR263-13, Olfr118
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.070) question?
Stock # R9778 (G1)
Quality Score 225.009
Status Not validated
Chromosome 17
Chromosomal Location 37982916-37983888 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 37983145 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Asparagine at position 77 (I77N)
Ref Sequence ENSEMBL: ENSMUSP00000150176 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000122036] [ENSMUST00000215811] [ENSMUST00000216551]
AlphaFold Q7TRJ6
Predicted Effect probably damaging
Transcript: ENSMUST00000122036
AA Change: I77N

PolyPhen 2 Score 0.972 (Sensitivity: 0.77; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000113988
Gene: ENSMUSG00000080990
AA Change: I77N

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srv 32 173 2e-6 PFAM
Pfam:7tm_4 37 314 2.1e-57 PFAM
Pfam:7TM_GPCR_Srsx 41 311 5.8e-6 PFAM
Pfam:7tm_1 47 296 1.4e-24 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000215811
AA Change: I77N

PolyPhen 2 Score 0.972 (Sensitivity: 0.77; Specificity: 0.96)
Predicted Effect probably damaging
Transcript: ENSMUST00000216551
AA Change: I77N

PolyPhen 2 Score 0.972 (Sensitivity: 0.77; Specificity: 0.96)
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.8%
  • 10x: 99.4%
  • 20x: 98.5%
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: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310022B05Rik A T 8: 125,366,098 (GRCm39) I215N probably damaging Het
Aig1 T C 10: 13,528,757 (GRCm39) probably null Het
Atp8b2 T A 3: 89,861,865 (GRCm39) K82N possibly damaging Het
Cacnb4 T G 2: 52,359,615 (GRCm39) Y131S probably damaging Het
Cep170b G A 12: 112,697,864 (GRCm39) S62N possibly damaging Het
Crmp1 A G 5: 37,422,619 (GRCm39) D142G probably benign Het
Csf1r A G 18: 61,260,957 (GRCm39) Q716R possibly damaging Het
Cyp2u1 T C 3: 131,087,133 (GRCm39) T483A possibly damaging Het
D930020B18Rik T C 10: 121,503,565 (GRCm39) F247L probably benign Het
Dcaf13 T C 15: 39,008,586 (GRCm39) L396P probably damaging Het
Dnhd1 A G 7: 105,353,240 (GRCm39) M2798V probably benign Het
E030018B13Rik A T 7: 63,569,125 (GRCm39) T58S unknown Het
Eipr1 T C 12: 28,897,657 (GRCm39) probably null Het
Elf1 C T 14: 79,817,948 (GRCm39) T526M possibly damaging Het
Gm8369 GTGTGTGTGTGTGTGTGTGTG GTGTGTGTGTGTGTGTGTGTGTG 19: 11,489,128 (GRCm39) probably null Het
Got1 A G 19: 43,504,284 (GRCm39) S46P probably benign Het
Inpp4b T C 8: 82,775,160 (GRCm39) I786T probably benign Het
Kdm1a T C 4: 136,279,892 (GRCm39) I703M probably damaging Het
Krt222 A T 11: 99,125,838 (GRCm39) S264R probably benign Het
Lrrd1 A C 5: 3,899,982 (GRCm39) S96R possibly damaging Het
Ltb C A 17: 35,414,906 (GRCm39) Y235* probably null Het
Mbd2 T A 18: 70,751,050 (GRCm39) C362S probably damaging Het
Mlycd T A 8: 120,129,325 (GRCm39) I264N probably damaging Het
Mri1 C T 8: 84,980,933 (GRCm39) C199Y possibly damaging Het
Muc5ac A T 7: 141,349,021 (GRCm39) K487* probably null Het
Myh13 T C 11: 67,249,016 (GRCm39) I1274T probably damaging Het
Ncdn G A 4: 126,642,467 (GRCm39) R397W probably damaging Het
Ncf1 T A 5: 134,258,444 (GRCm39) probably benign Het
Nipbl C A 15: 8,321,032 (GRCm39) A2692S probably benign Het
Odf2l C T 3: 144,854,789 (GRCm39) T542I possibly damaging Het
Or10a49 A G 7: 108,467,698 (GRCm39) I221T probably damaging Het
Oxsm T C 14: 16,242,629 (GRCm38) T47A possibly damaging Het
Pcdhga3 A T 18: 37,807,786 (GRCm39) S80C probably benign Het
Pcnx2 T C 8: 126,512,176 (GRCm39) T1377A probably benign Het
Phactr3 C A 2: 177,924,805 (GRCm39) Q252K possibly damaging Het
Phf2 T C 13: 48,973,101 (GRCm39) H385R unknown Het
Pkd1l3 A T 8: 110,357,937 (GRCm39) T820S probably benign Het
Plekhg1 T A 10: 3,887,966 (GRCm39) H353Q Het
Prss37 T A 6: 40,494,713 (GRCm39) E24V probably damaging Het
Reln A G 5: 22,155,943 (GRCm39) F2183S probably damaging Het
Slc20a2 A G 8: 23,051,407 (GRCm39) D480G probably damaging Het
Slc8a2 C T 7: 15,887,124 (GRCm39) T672M probably damaging Het
Slf2 A G 19: 44,961,666 (GRCm39) T1062A probably benign Het
Snx29 A G 16: 11,223,609 (GRCm39) E18G possibly damaging Het
Spata31e1 C T 13: 49,939,542 (GRCm39) V723M possibly damaging Het
Srf C A 17: 46,860,079 (GRCm39) G482V possibly damaging Het
Styk1 G A 6: 131,287,992 (GRCm39) Q124* probably null Het
Tcf7l1 G T 6: 72,608,226 (GRCm39) A385E probably damaging Het
Thbs4 A G 13: 92,913,495 (GRCm39) S142P probably benign Het
Tlr1 G A 5: 65,083,371 (GRCm39) S402F probably damaging Het
Tnrc6a A G 7: 122,769,635 (GRCm39) H475R probably benign Het
Trmt10b A T 4: 45,314,374 (GRCm39) N272I probably damaging Het
Ubxn7 A T 16: 32,200,471 (GRCm39) N409I probably benign Het
Vcan T C 13: 89,837,930 (GRCm39) E2538G probably damaging Het
Vmn1r65 C T 7: 6,011,387 (GRCm39) W282* probably null Het
Vmn2r4 A G 3: 64,322,497 (GRCm39) I74T probably benign Het
Wdr97 T A 15: 76,241,125 (GRCm39) F574I Het
Zfp949 T C 9: 88,449,340 (GRCm39) probably null Het
Other mutations in Or10al2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01300:Or10al2 APN 17 37,983,778 (GRCm39) missense probably damaging 1.00
IGL02456:Or10al2 APN 17 37,983,340 (GRCm39) missense possibly damaging 0.90
IGL02750:Or10al2 APN 17 37,983,500 (GRCm39) nonsense probably null
IGL03083:Or10al2 APN 17 37,983,551 (GRCm39) nonsense probably null
IGL03339:Or10al2 APN 17 37,983,448 (GRCm39) missense possibly damaging 0.87
R0032:Or10al2 UTSW 17 37,983,378 (GRCm39) missense probably damaging 1.00
R1457:Or10al2 UTSW 17 37,983,816 (GRCm39) nonsense probably null
R1542:Or10al2 UTSW 17 37,983,142 (GRCm39) missense probably damaging 1.00
R1771:Or10al2 UTSW 17 37,983,554 (GRCm39) missense probably damaging 1.00
R1893:Or10al2 UTSW 17 37,983,747 (GRCm39) nonsense probably null
R2395:Or10al2 UTSW 17 37,983,587 (GRCm39) nonsense probably null
R3619:Or10al2 UTSW 17 37,983,531 (GRCm39) missense probably benign 0.05
R3917:Or10al2 UTSW 17 37,983,684 (GRCm39) missense probably damaging 1.00
R3937:Or10al2 UTSW 17 37,983,858 (GRCm39) missense probably benign 0.01
R5600:Or10al2 UTSW 17 37,983,176 (GRCm39) missense possibly damaging 0.91
R6415:Or10al2 UTSW 17 37,983,448 (GRCm39) missense possibly damaging 0.87
R6462:Or10al2 UTSW 17 37,983,111 (GRCm39) missense probably damaging 1.00
R7355:Or10al2 UTSW 17 37,983,301 (GRCm39) missense probably benign 0.02
R7861:Or10al2 UTSW 17 37,983,408 (GRCm39) missense possibly damaging 0.91
R7913:Or10al2 UTSW 17 37,982,999 (GRCm39) missense probably benign
R7952:Or10al2 UTSW 17 37,983,708 (GRCm39) missense probably damaging 1.00
R7969:Or10al2 UTSW 17 37,983,547 (GRCm39) missense probably damaging 1.00
R8879:Or10al2 UTSW 17 37,983,302 (GRCm39) nonsense probably null
R8923:Or10al2 UTSW 17 37,983,702 (GRCm39) missense probably benign 0.00
R9253:Or10al2 UTSW 17 37,983,637 (GRCm39) missense probably benign 0.00
R9789:Or10al2 UTSW 17 37,983,059 (GRCm39) missense probably damaging 1.00
RF003:Or10al2 UTSW 17 37,983,749 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GAGTGTCAACTGCTCTCTGTG -3'
(R):5'- GGGAGCATATGGCCATGTAG -3'

Sequencing Primer
(F):5'- TGCTCTCTGTGGCAGGAGAAC -3'
(R):5'- AGCATATGGCCATGTAGCGGTC -3'
Posted On 2022-11-14