Incidental Mutation 'R5773:Or10ak9'
ID 445491
Institutional Source Beutler Lab
Gene Symbol Or10ak9
Ensembl Gene ENSMUSG00000073769
Gene Name olfactory receptor family 10 subfamily AK member 9
Synonyms MOR259-3P, GA_x6K02T2QD9B-18670866-18669913, Olfr1331
MMRRC Submission 043372-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.059) question?
Stock # R5773 (G1)
Quality Score 225
Status Not validated
Chromosome 4
Chromosomal Location 118725980-118726933 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 118726718 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 247 (T247A)
Ref Sequence ENSEMBL: ENSMUSP00000101967 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094831] [ENSMUST00000106360] [ENSMUST00000216589]
AlphaFold K7N684
Predicted Effect probably damaging
Transcript: ENSMUST00000094831
AA Change: T247A

PolyPhen 2 Score 0.970 (Sensitivity: 0.77; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000092426
Gene: ENSMUSG00000073769
AA Change: T247A

DomainStartEndE-ValueType
Pfam:7tm_4 32 308 2.1e-53 PFAM
Pfam:7tm_1 42 291 3.9e-22 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000106360
AA Change: T247A

PolyPhen 2 Score 0.970 (Sensitivity: 0.77; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000101967
Gene: ENSMUSG00000073769
AA Change: T247A

DomainStartEndE-ValueType
Pfam:7tm_1 41 290 1.2e-28 PFAM
Pfam:7tm_4 139 283 2.8e-45 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000216589
AA Change: T246A

PolyPhen 2 Score 0.963 (Sensitivity: 0.78; Specificity: 0.95)
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.8%
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: 57 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acss2 G A 2: 155,416,614 (GRCm39) probably null Het
Akna C T 4: 63,313,307 (GRCm39) S272N probably benign Het
Ap2m1 T C 16: 20,362,140 (GRCm39) V416A probably damaging Het
Atp7b A G 8: 22,517,879 (GRCm39) F320L probably benign Het
Brd1 T C 15: 88,573,752 (GRCm39) K1116E probably benign Het
Ccdc186 T C 19: 56,801,919 (GRCm39) D66G probably benign Het
Cdh4 A G 2: 179,527,789 (GRCm39) Y503C probably damaging Het
Cfb C A 17: 35,076,248 (GRCm39) E166* probably null Het
Cmtm1 A T 8: 105,031,808 (GRCm39) F90I probably damaging Het
Col1a1 A T 11: 94,830,255 (GRCm39) K160N probably benign Het
Cradd T C 10: 95,011,823 (GRCm39) I106V probably benign Het
Defa17 A G 8: 22,146,574 (GRCm39) R67G probably damaging Het
Dgkh T C 14: 78,832,895 (GRCm39) N765S probably damaging Het
Dock5 A G 14: 68,033,507 (GRCm39) V954A possibly damaging Het
Eif2d A G 1: 131,086,040 (GRCm39) probably null Het
Epg5 T A 18: 78,004,040 (GRCm39) F683I probably damaging Het
Fhad1 T G 4: 141,656,881 (GRCm39) K91T probably damaging Het
Fut11 A T 14: 20,748,383 (GRCm39) D476V probably damaging Het
Gldn T C 9: 54,241,775 (GRCm39) probably null Het
Gm7247 C T 14: 51,601,805 (GRCm39) S26F probably benign Het
Gm8674 T A 13: 50,055,912 (GRCm39) noncoding transcript Het
Gtpbp6 C A 5: 110,254,757 (GRCm39) E168D possibly damaging Het
Hinfp T A 9: 44,210,533 (GRCm39) H163L probably benign Het
Igkv6-29 C A 6: 70,115,584 (GRCm39) G70V possibly damaging Het
Ing3 T A 6: 21,971,834 (GRCm39) C368S probably damaging Het
Itih1 A G 14: 30,657,356 (GRCm39) V489A possibly damaging Het
Itsn2 T C 12: 4,757,089 (GRCm39) L1393P probably damaging Het
Kcnj13 T C 1: 87,314,389 (GRCm39) T278A probably damaging Het
Kntc1 G A 5: 123,932,220 (GRCm39) R1338Q probably damaging Het
Lipi T A 16: 75,370,813 (GRCm39) T135S probably damaging Het
Map7 A G 10: 20,122,390 (GRCm39) K152R probably benign Het
Mmp24 A G 2: 155,641,829 (GRCm39) Y219C probably damaging Het
Nup188 T C 2: 30,212,208 (GRCm39) V565A possibly damaging Het
Nup210 T C 6: 91,062,865 (GRCm39) K265E probably damaging Het
Pcdha6 A T 18: 37,102,643 (GRCm39) H612L probably benign Het
Pgpep1 G A 8: 71,105,101 (GRCm39) T53M probably damaging Het
Pld2 G T 11: 70,446,758 (GRCm39) S778I probably damaging Het
Ppef2 A C 5: 92,398,420 (GRCm39) Y33D probably damaging Het
Ppfibp2 A T 7: 107,285,079 (GRCm39) T129S possibly damaging Het
Prickle1 G T 15: 93,406,478 (GRCm39) H182N probably damaging Het
R3hdm2 T A 10: 127,280,172 (GRCm39) probably benign Het
Rbm12b1 A T 4: 12,145,765 (GRCm39) E579V probably damaging Het
Rsf1 GGC GGCGGCGGCTGC 7: 97,229,140 (GRCm39) probably benign Het
Slc1a6 T G 10: 78,629,111 (GRCm39) probably null Het
Slc27a6 G T 18: 58,715,245 (GRCm39) A283S probably damaging Het
Spats2l T A 1: 57,918,708 (GRCm39) N27K possibly damaging Het
Srgap1 T C 10: 121,732,614 (GRCm39) M155V probably benign Het
Stxbp5l C A 16: 37,028,459 (GRCm39) A535S probably damaging Het
Svep1 C A 4: 58,099,985 (GRCm39) C1353F possibly damaging Het
Taar4 T A 10: 23,837,056 (GRCm39) I222N probably damaging Het
Tlr6 A G 5: 65,111,846 (GRCm39) F354L probably benign Het
Trp53bp1 A G 2: 121,074,395 (GRCm39) S452P probably damaging Het
Ttll5 GCCCTGCGGGGCTGCCACGCTGTCGATCCGGCAGCTAC G 12: 85,980,329 (GRCm39) probably null Het
Usp42 A T 5: 143,699,467 (GRCm39) M1264K probably benign Het
Zfp865 A T 7: 5,037,693 (GRCm39) probably benign Het
Zfyve26 A T 12: 79,334,511 (GRCm39) L169Q probably damaging Het
Zmym4 A T 4: 126,799,163 (GRCm39) N383K possibly damaging Het
Other mutations in Or10ak9
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00090:Or10ak9 APN 4 118,726,484 (GRCm39) missense probably damaging 1.00
IGL01314:Or10ak9 APN 4 118,726,328 (GRCm39) missense probably benign 0.26
IGL02025:Or10ak9 APN 4 118,726,362 (GRCm39) missense probably damaging 1.00
IGL02458:Or10ak9 APN 4 118,726,497 (GRCm39) missense possibly damaging 0.83
IGL02793:Or10ak9 APN 4 118,726,794 (GRCm39) missense probably damaging 1.00
IGL02827:Or10ak9 APN 4 118,726,157 (GRCm39) missense probably damaging 0.99
IGL02863:Or10ak9 APN 4 118,726,083 (GRCm39) missense possibly damaging 0.52
IGL03125:Or10ak9 APN 4 118,726,118 (GRCm39) missense possibly damaging 0.95
R0078:Or10ak9 UTSW 4 118,726,424 (GRCm39) missense probably benign
R0152:Or10ak9 UTSW 4 118,726,083 (GRCm39) missense possibly damaging 0.89
R0299:Or10ak9 UTSW 4 118,726,613 (GRCm39) missense probably benign 0.00
R3881:Or10ak9 UTSW 4 118,726,550 (GRCm39) missense probably benign 0.00
R3928:Or10ak9 UTSW 4 118,726,179 (GRCm39) missense probably damaging 1.00
R3929:Or10ak9 UTSW 4 118,726,179 (GRCm39) missense probably damaging 1.00
R5288:Or10ak9 UTSW 4 118,726,772 (GRCm39) missense probably damaging 1.00
R5552:Or10ak9 UTSW 4 118,726,665 (GRCm39) missense probably damaging 1.00
R5672:Or10ak9 UTSW 4 118,726,379 (GRCm39) missense possibly damaging 0.83
R6117:Or10ak9 UTSW 4 118,726,341 (GRCm39) missense probably benign 0.39
R6910:Or10ak9 UTSW 4 118,726,335 (GRCm39) missense probably damaging 1.00
R6911:Or10ak9 UTSW 4 118,726,335 (GRCm39) missense probably damaging 1.00
R6912:Or10ak9 UTSW 4 118,726,335 (GRCm39) missense probably damaging 1.00
R7164:Or10ak9 UTSW 4 118,726,922 (GRCm39) missense probably benign 0.30
R7446:Or10ak9 UTSW 4 118,726,019 (GRCm39) missense possibly damaging 0.83
R9747:Or10ak9 UTSW 4 118,726,217 (GRCm39) missense probably damaging 1.00
T0975:Or10ak9 UTSW 4 118,726,500 (GRCm39) missense probably benign 0.02
Predicted Primers PCR Primer
(F):5'- AACAGGGTCAACCACTACTTGTG -3'
(R):5'- TCACCTTGAGAAATGCCCTC -3'

Sequencing Primer
(F):5'- GTCAACCACTACTTGTGTGAAGGTC -3'
(R):5'- ACCTTGAGAAATGCCCTCTTGATG -3'
Posted On 2016-11-21