Incidental Mutation 'R2897:Or10aa1'
ID 260823
Institutional Source Beutler Lab
Gene Symbol Or10aa1
Ensembl Gene ENSMUSG00000045381
Gene Name olfactory receptor family 10 subfamily AA member 1
Synonyms GA_x6K02T2P20D-21133014-21132070, Olfr433, MOR123-1
MMRRC Submission 040485-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.057) question?
Stock # R2897 (G1)
Quality Score 225
Status Validated
Chromosome 1
Chromosomal Location 173869499-173870502 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 173869699 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Serine at position 61 (F61S)
Ref Sequence ENSEMBL: ENSMUSP00000149005 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000052975] [ENSMUST00000214690]
AlphaFold Q7TRV9
Predicted Effect probably damaging
Transcript: ENSMUST00000052975
AA Change: F61S

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000056772
Gene: ENSMUSG00000045381
AA Change: F61S

DomainStartEndE-ValueType
Pfam:7tm_4 31 306 4.6e-51 PFAM
Pfam:7TM_GPCR_Srsx 35 170 2.9e-8 PFAM
Pfam:7tm_1 41 289 1.3e-20 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000214690
AA Change: F61S

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.7%
  • 10x: 97.5%
  • 20x: 95.8%
Validation Efficiency 99% (72/73)
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: 72 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2210408I21Rik T C 13: 77,471,640 (GRCm39) V1015A probably benign Het
4930480E11Rik C T X: 77,413,868 (GRCm39) Q198* probably null Het
Acap3 G C 4: 155,989,388 (GRCm39) probably null Het
Adamts14 T C 10: 61,040,689 (GRCm39) D879G probably damaging Het
Akap1 A T 11: 88,735,605 (GRCm39) C352* probably null Het
Ankk1 T A 9: 49,333,122 (GRCm39) T121S probably benign Het
Ankrd6 T C 4: 32,860,438 (GRCm39) S2G probably damaging Het
Anks1 G T 17: 28,204,337 (GRCm39) probably null Het
Apob G A 12: 8,060,356 (GRCm39) G2946D probably damaging Het
Atm A C 9: 53,419,105 (GRCm39) C782W probably damaging Het
Atp1a4 A T 1: 172,074,257 (GRCm39) I332N probably damaging Het
Bnc2 T C 4: 84,211,152 (GRCm39) I406V probably damaging Het
Cdh20 A T 1: 104,875,199 (GRCm39) D327V probably damaging Het
Cep192 T A 18: 67,988,341 (GRCm39) probably null Het
Chd5 T C 4: 152,456,572 (GRCm39) F970L probably damaging Het
Coq9 T C 8: 95,579,752 (GRCm39) Y236H probably damaging Het
Csn1s2a A G 5: 87,929,680 (GRCm39) H93R unknown Het
Cxcr2 T C 1: 74,198,130 (GRCm39) V208A probably benign Het
Cyp1b1 G A 17: 80,021,160 (GRCm39) T194M probably benign Het
Dbt T A 3: 116,317,061 (GRCm39) V79E probably damaging Het
Dcx A G X: 142,706,428 (GRCm39) probably benign Het
Dnm3 G A 1: 162,113,643 (GRCm39) probably benign Het
Erbin C T 13: 104,022,705 (GRCm39) E45K probably damaging Het
Fastkd1 A G 2: 69,532,960 (GRCm39) L469P probably damaging Het
Gkn3 C T 6: 87,360,507 (GRCm39) A163T probably damaging Het
Gm10271 A G 10: 116,808,495 (GRCm39) L7S probably damaging Het
Gm5087 T C 14: 13,158,805 (GRCm38) noncoding transcript Het
Hid1 A G 11: 115,241,356 (GRCm39) S645P probably benign Het
Hmcn1 C T 1: 150,678,624 (GRCm39) C499Y probably damaging Het
Ifna1 C A 4: 88,768,450 (GRCm39) Q43K probably benign Het
Ikbkb G T 8: 23,159,693 (GRCm39) Q432K possibly damaging Het
Inpp4a A T 1: 37,405,675 (GRCm39) H148L probably benign Het
Itpr2 C T 6: 146,074,839 (GRCm39) R2338Q probably benign Het
Itpr2 A T 6: 146,224,667 (GRCm39) I1441N probably damaging Het
Krt78 T C 15: 101,855,541 (GRCm39) R757G probably benign Het
Lmx1a T A 1: 167,658,109 (GRCm39) probably benign Het
Lpxn T A 19: 12,796,722 (GRCm39) S81T probably benign Het
Lrriq1 T C 10: 103,063,111 (GRCm39) N65S probably damaging Het
Mis18bp1 T C 12: 65,180,360 (GRCm39) D981G probably benign Het
Mpp4 T C 1: 59,183,853 (GRCm39) I296V probably benign Het
Mtrf1l T C 10: 5,767,565 (GRCm39) R184G probably benign Het
Muc19 T C 15: 91,822,550 (GRCm39) noncoding transcript Het
Myo6 T A 9: 80,176,893 (GRCm39) probably null Het
Myom1 A G 17: 71,408,215 (GRCm39) probably benign Het
Ndrg4 A G 8: 96,405,014 (GRCm39) probably null Het
Neu2 A G 1: 87,522,782 (GRCm39) S72G probably benign Het
Nlrc4 T A 17: 74,755,040 (GRCm39) M59L probably benign Het
Nuak2 A T 1: 132,252,791 (GRCm39) H115L probably damaging Het
Oog1 T A 12: 87,655,178 (GRCm39) I272K probably damaging Het
Or52a20 A T 7: 103,366,749 (GRCm39) Y316F probably benign Het
Pcdhb1 A G 18: 37,399,516 (GRCm39) Y489C probably damaging Het
Pde5a T C 3: 122,572,651 (GRCm39) I344T probably benign Het
Pip5kl1 C A 2: 32,473,359 (GRCm39) A332D probably benign Het
Pja1 T C X: 98,510,754 (GRCm39) E385G probably benign Het
Psma6 A T 12: 55,454,829 (GRCm39) I53L probably benign Het
Ric8b T G 10: 84,783,761 (GRCm39) D206E probably benign Het
Sardh T C 2: 27,079,559 (GRCm39) D911G probably benign Het
Serpinb8 A G 1: 107,534,776 (GRCm39) T32A unknown Het
Shroom2 G T X: 151,443,035 (GRCm39) T710K probably benign Het
Shroom3 G T 5: 93,090,945 (GRCm39) V1151F probably damaging Het
Slc38a7 A G 8: 96,572,424 (GRCm39) probably benign Het
Stk36 T A 1: 74,671,984 (GRCm39) S895T probably null Het
Sycp3 G A 10: 88,308,544 (GRCm39) E205K possibly damaging Het
Tbc1d16 A T 11: 119,048,654 (GRCm39) I333N probably damaging Het
Tectb C G 19: 55,169,431 (GRCm39) probably benign Het
Tmeff1 T A 4: 48,658,831 (GRCm39) Y101* probably null Het
Tns2 C T 15: 102,017,369 (GRCm39) R281C probably damaging Het
Ttn T A 2: 76,549,500 (GRCm39) T23399S probably damaging Het
Vipas39 A G 12: 87,289,297 (GRCm39) V389A possibly damaging Het
Vps41 T C 13: 18,994,598 (GRCm39) probably benign Het
Zfp329 A T 7: 12,544,413 (GRCm39) H370Q probably damaging Het
Zfp37 C T 4: 62,110,014 (GRCm39) G350D probably damaging Het
Other mutations in Or10aa1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01760:Or10aa1 APN 1 173,870,191 (GRCm39) missense probably damaging 0.99
IGL02369:Or10aa1 APN 1 173,869,539 (GRCm39) missense possibly damaging 0.64
IGL03256:Or10aa1 APN 1 173,869,774 (GRCm39) missense probably damaging 1.00
IGL03297:Or10aa1 APN 1 173,869,683 (GRCm39) missense probably benign 0.00
R0837:Or10aa1 UTSW 1 173,870,053 (GRCm39) missense probably damaging 1.00
R1583:Or10aa1 UTSW 1 173,870,046 (GRCm39) missense probably benign 0.11
R1974:Or10aa1 UTSW 1 173,870,154 (GRCm39) missense probably damaging 1.00
R2280:Or10aa1 UTSW 1 173,870,087 (GRCm39) missense probably benign 0.00
R3022:Or10aa1 UTSW 1 173,869,650 (GRCm39) missense probably benign 0.13
R4478:Or10aa1 UTSW 1 173,870,182 (GRCm39) missense probably benign 0.00
R6364:Or10aa1 UTSW 1 173,869,778 (GRCm39) missense possibly damaging 0.80
R6588:Or10aa1 UTSW 1 173,869,844 (GRCm39) missense probably benign 0.01
R7343:Or10aa1 UTSW 1 173,870,419 (GRCm39) missense probably damaging 0.98
R7409:Or10aa1 UTSW 1 173,870,099 (GRCm39) missense probably benign 0.02
R7714:Or10aa1 UTSW 1 173,869,900 (GRCm39) missense probably benign 0.00
R7788:Or10aa1 UTSW 1 173,869,650 (GRCm39) missense probably benign 0.13
R8982:Or10aa1 UTSW 1 173,870,188 (GRCm39) missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- CTCCTTGGAACCATGGATCATG -3'
(R):5'- TGCAGTGGACGACAGATAGC -3'

Sequencing Primer
(F):5'- TGGATCATGTCAACTACACCTGG -3'
(R):5'- TAGCGGTCCAGAGCCATGAC -3'
Posted On 2015-01-23