Incidental Mutation 'R9112:Or6ae1'
ID 692301
Institutional Source Beutler Lab
Gene Symbol Or6ae1
Ensembl Gene ENSMUSG00000051180
Gene Name olfactory receptor family 6 subfamily AE member 1
Synonyms Olfr522, GA_x6K02T2PBJ9-42315125-42314187, MOR103-5
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.061) question?
Stock # R9112 (G1)
Quality Score 225.009
Status Validated
Chromosome 7
Chromosomal Location 139741923-139742861 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 139742660 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 68 (S68P)
Ref Sequence ENSEMBL: ENSMUSP00000057288 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000050585]
AlphaFold Q8VGL1
Predicted Effect
SMART Domains Protein: ENSMUSP00000057288
Gene: ENSMUSG00000051180
AA Change: S68P

DomainStartEndE-ValueType
Pfam:7tm_4 32 308 1.7e-54 PFAM
Pfam:7tm_1 42 291 1.2e-21 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.3%
Validation Efficiency 100% (56/56)
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: 60 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310033P09Rik A G 11: 59,100,806 (GRCm39) S181G possibly damaging Het
5730596B20Rik A G 6: 52,156,413 (GRCm39) R160G unknown Het
Acy1 A G 9: 106,311,952 (GRCm39) Y262H probably benign Het
Adamts13 T C 2: 26,880,379 (GRCm39) S681P possibly damaging Het
Adgra3 C A 5: 50,118,395 (GRCm39) C1051F probably damaging Het
Afp T C 5: 90,652,289 (GRCm39) probably null Het
Agrn A T 4: 156,261,514 (GRCm39) V568E probably damaging Het
Ahnak A G 19: 8,987,149 (GRCm39) E2811G probably damaging Het
Ap1m1 C A 8: 72,994,066 (GRCm39) Y7* probably null Het
Apobec1 T A 6: 122,555,837 (GRCm39) T207S probably benign Het
Arhgap32 G A 9: 32,157,309 (GRCm39) R102Q probably damaging Het
Bcat2 T C 7: 45,237,446 (GRCm39) probably null Het
Cd209f T A 8: 4,155,802 (GRCm39) probably benign Het
Cox7c G A 13: 86,194,837 (GRCm39) probably benign Het
Cyp2d11 A G 15: 82,276,203 (GRCm39) V156A possibly damaging Het
Dhrs3 A T 4: 144,653,769 (GRCm39) T297S probably benign Het
Dip2c T C 13: 9,660,766 (GRCm39) C876R probably damaging Het
Eprs1 A T 1: 185,129,273 (GRCm39) I587F probably damaging Het
Fam13c A G 10: 70,286,978 (GRCm39) T81A probably benign Het
Flt4 A G 11: 49,524,064 (GRCm39) Y548C probably damaging Het
Garin2 T C 12: 78,757,202 (GRCm39) probably null Het
Gimap4 T A 6: 48,667,629 (GRCm39) V128E probably benign Het
Gm32742 A G 9: 51,060,735 (GRCm39) L856P possibly damaging Het
Gm5916 A G 9: 36,032,258 (GRCm39) Y59H probably damaging Het
Gnai3 A T 3: 108,030,990 (GRCm39) H57Q Het
Golga3 G T 5: 110,333,757 (GRCm39) R131L probably benign Het
Gpc6 A T 14: 117,424,088 (GRCm39) I59F probably benign Het
H2bc6 T C 13: 23,769,753 (GRCm39) M63V possibly damaging Het
Herc6 T C 6: 57,596,604 (GRCm39) S515P probably damaging Het
Ift74 T C 4: 94,575,103 (GRCm39) I518T probably benign Het
Kat6b T C 14: 21,675,256 (GRCm39) S474P possibly damaging Het
Klhl3 A C 13: 58,248,212 (GRCm39) I28S unknown Het
Klrh1 T A 6: 129,743,697 (GRCm39) I196F probably benign Het
Lipi A G 16: 75,359,159 (GRCm39) F259S probably damaging Het
Lrrc8a T A 2: 30,145,782 (GRCm39) S199T probably damaging Het
Map2 T A 1: 66,472,723 (GRCm39) C1709* probably null Het
Mrgprf A G 7: 144,861,503 (GRCm39) S22G probably benign Het
Myo1e G T 9: 70,274,983 (GRCm39) R712L probably benign Het
Nras A T 3: 102,967,658 (GRCm39) N85Y probably benign Het
Or4a71 C T 2: 89,358,337 (GRCm39) C139Y probably damaging Het
Or5b3 A T 19: 13,388,475 (GRCm39) I181F probably benign Het
Or9q2 T C 19: 13,772,780 (GRCm39) H65R probably damaging Het
Pcp2 T A 8: 3,674,638 (GRCm39) probably benign Het
Pigv T C 4: 133,392,079 (GRCm39) R364G probably benign Het
Plekhh3 T A 11: 101,061,625 (GRCm39) S30C probably damaging Het
Poglut3 A G 9: 53,295,530 (GRCm39) Y44C probably damaging Het
Pramel11 A C 4: 143,623,334 (GRCm39) V280G possibly damaging Het
Pramel51 C T 12: 88,144,055 (GRCm39) A261T possibly damaging Het
Rhof T C 5: 123,258,571 (GRCm39) probably benign Het
Rufy3 A T 5: 88,780,336 (GRCm39) E361D Het
Serpina1b T C 12: 103,698,699 (GRCm39) D50G probably benign Het
Sgsm2 G A 11: 74,756,222 (GRCm39) Q376* probably null Het
Slc18b1 A T 10: 23,692,262 (GRCm39) I246F probably damaging Het
Slc38a9 A T 13: 112,850,777 (GRCm39) N387I probably damaging Het
Synrg C G 11: 83,862,409 (GRCm39) P35A probably damaging Het
Tdrp T C 8: 14,005,796 (GRCm39) K42E probably damaging Het
Trappc10 A C 10: 78,029,201 (GRCm39) M1112R probably damaging Het
Ube2e1 A G 14: 18,285,203 (GRCm38) V90A probably damaging Het
Vwde C A 6: 13,205,051 (GRCm39) V277F possibly damaging Het
Zfyve16 A G 13: 92,659,563 (GRCm39) M116T possibly damaging Het
Other mutations in Or6ae1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01806:Or6ae1 APN 7 139,742,841 (GRCm39) missense probably benign 0.01
IGL02121:Or6ae1 APN 7 139,742,607 (GRCm39) missense probably benign 0.10
IGL02399:Or6ae1 APN 7 139,742,513 (GRCm39) missense probably benign
IGL02803:Or6ae1 APN 7 139,742,287 (GRCm39) missense possibly damaging 0.92
R0446:Or6ae1 UTSW 7 139,742,384 (GRCm39) missense probably damaging 1.00
R0538:Or6ae1 UTSW 7 139,742,144 (GRCm39) missense probably damaging 1.00
R0707:Or6ae1 UTSW 7 139,742,002 (GRCm39) missense probably damaging 1.00
R1466:Or6ae1 UTSW 7 139,742,116 (GRCm39) missense probably damaging 1.00
R1466:Or6ae1 UTSW 7 139,742,116 (GRCm39) missense probably damaging 1.00
R1584:Or6ae1 UTSW 7 139,742,116 (GRCm39) missense probably damaging 1.00
R1893:Or6ae1 UTSW 7 139,742,734 (GRCm39) missense probably damaging 1.00
R1895:Or6ae1 UTSW 7 139,742,726 (GRCm39) missense possibly damaging 0.82
R2004:Or6ae1 UTSW 7 139,742,729 (GRCm39) missense probably damaging 0.98
R2060:Or6ae1 UTSW 7 139,742,737 (GRCm39) missense probably damaging 1.00
R2067:Or6ae1 UTSW 7 139,742,822 (GRCm39) missense possibly damaging 0.69
R4841:Or6ae1 UTSW 7 139,742,602 (GRCm39) missense possibly damaging 0.94
R4842:Or6ae1 UTSW 7 139,742,602 (GRCm39) missense possibly damaging 0.94
R4956:Or6ae1 UTSW 7 139,741,993 (GRCm39) missense possibly damaging 0.70
R5189:Or6ae1 UTSW 7 139,742,632 (GRCm39) missense probably damaging 0.98
R5325:Or6ae1 UTSW 7 139,742,026 (GRCm39) missense probably damaging 1.00
R5441:Or6ae1 UTSW 7 139,742,564 (GRCm39) missense probably benign 0.36
R5618:Or6ae1 UTSW 7 139,742,185 (GRCm39) missense probably damaging 1.00
R6031:Or6ae1 UTSW 7 139,742,722 (GRCm39) missense possibly damaging 0.82
R6031:Or6ae1 UTSW 7 139,742,722 (GRCm39) missense possibly damaging 0.82
R6609:Or6ae1 UTSW 7 139,742,476 (GRCm39) missense probably benign
R7154:Or6ae1 UTSW 7 139,741,997 (GRCm39) missense probably benign 0.00
R8370:Or6ae1 UTSW 7 139,742,681 (GRCm39) missense probably damaging 0.98
R8765:Or6ae1 UTSW 7 139,742,467 (GRCm39) missense probably benign
R9002:Or6ae1 UTSW 7 139,742,198 (GRCm39) missense probably damaging 0.99
R9431:Or6ae1 UTSW 7 139,741,942 (GRCm39) missense probably benign 0.04
R9513:Or6ae1 UTSW 7 139,742,822 (GRCm39) missense possibly damaging 0.69
R9563:Or6ae1 UTSW 7 139,742,233 (GRCm39) missense probably damaging 1.00
R9641:Or6ae1 UTSW 7 139,742,771 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- TGAATCCATGATGGCTGGGTAG -3'
(R):5'- CAACGCTTTGGTGACAGAGTTC -3'

Sequencing Primer
(F):5'- GTAGTGCAGTGGACGGC -3'
(R):5'- GACAGAGTTCATTCTTCTGGGTTTCC -3'
Posted On 2021-12-30