Incidental Mutation 'IGL02728:Or9r3'
ID 305294
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or9r3
Ensembl Gene ENSMUSG00000096747
Gene Name olfactory receptor family 9 subfamily R member 3
Synonyms Olfr823, MOR210-4, GA_x6K02T2PULF-11783479-11782532
Accession Numbers
Essential gene? Probably non essential (E-score: 0.081) question?
Stock # IGL02728
Quality Score
Status
Chromosome 10
Chromosomal Location 129947710-129948657 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 129948487 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Serine at position 57 (R57S)
Ref Sequence ENSEMBL: ENSMUSP00000150794 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000081469] [ENSMUST00000213145]
AlphaFold Q7TRH2
Predicted Effect probably damaging
Transcript: ENSMUST00000081469
AA Change: R57S

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000080189
Gene: ENSMUSG00000096747
AA Change: R57S

DomainStartEndE-ValueType
Pfam:7tm_4 34 311 1.6e-54 PFAM
Pfam:7tm_1 44 293 7.6e-21 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000213145
AA Change: R57S

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
Coding Region Coverage
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: 72 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts7 G T 9: 90,073,880 (GRCm39) probably benign Het
Als2 A G 1: 59,235,506 (GRCm39) V726A probably benign Het
Apba1 G A 19: 23,922,269 (GRCm39) G779E possibly damaging Het
Atr T A 9: 95,818,528 (GRCm39) V2167E probably damaging Het
Bod1l T C 5: 41,983,846 (GRCm39) K566E probably damaging Het
Btd T C 14: 31,389,319 (GRCm39) F347L probably benign Het
Btg2 T C 1: 134,006,643 (GRCm39) probably benign Het
Cblb T A 16: 52,003,672 (GRCm39) S717T probably benign Het
Cep250 T A 2: 155,825,198 (GRCm39) probably benign Het
Cep350 T C 1: 155,828,968 (GRCm39) N312S probably benign Het
Clasp1 A T 1: 118,530,107 (GRCm39) T1490S probably damaging Het
Col7a1 T A 9: 108,813,172 (GRCm39) C2906S probably benign Het
Csmd1 C T 8: 16,049,779 (GRCm39) probably null Het
Cspg4 T A 9: 56,793,765 (GRCm39) V500E probably damaging Het
Cyp7b1 T A 3: 18,126,739 (GRCm39) D469V probably damaging Het
Dhh A T 15: 98,792,192 (GRCm39) probably null Het
Dhrs3 A G 4: 144,646,642 (GRCm39) R231G probably damaging Het
Disp3 A G 4: 148,356,495 (GRCm39) S122P probably damaging Het
Dnah1 T C 14: 31,005,955 (GRCm39) I2275V probably benign Het
Dock8 A C 19: 25,109,584 (GRCm39) N922T probably benign Het
Eef1d A G 15: 75,774,945 (GRCm39) L154P probably damaging Het
Eif4ebp1 C A 8: 27,763,510 (GRCm39) P101Q possibly damaging Het
Eif4g1 T G 16: 20,505,502 (GRCm39) probably benign Het
Emb A G 13: 117,369,301 (GRCm39) M50V probably benign Het
Eml4 T C 17: 83,780,568 (GRCm39) probably null Het
Fkbp10 G T 11: 100,306,803 (GRCm39) R65L probably damaging Het
Gm5878 T C 6: 85,095,574 (GRCm39) N83S probably benign Het
Gm8165 C T 14: 43,913,694 (GRCm39) A57T unknown Het
Gpr179 A G 11: 97,228,726 (GRCm39) V1143A probably damaging Het
Hat1 T C 2: 71,251,604 (GRCm39) Y218H probably damaging Het
Hfm1 T A 5: 107,026,689 (GRCm39) N885I probably benign Het
Ift70a1 T A 2: 75,811,193 (GRCm39) M297L probably benign Het
Inha T C 1: 75,486,091 (GRCm39) S129P probably damaging Het
Ints9 T C 14: 65,230,457 (GRCm39) I128T probably damaging Het
Klra9 T C 6: 130,168,149 (GRCm39) probably null Het
Lrba A G 3: 86,683,356 (GRCm39) E2726G probably damaging Het
Lrp1b T C 2: 40,691,410 (GRCm39) N3356D probably benign Het
Map3k5 A G 10: 19,994,038 (GRCm39) D1008G possibly damaging Het
Med4 T A 14: 73,755,415 (GRCm39) L241Q possibly damaging Het
Mtch1 A G 17: 29,557,716 (GRCm39) V254A possibly damaging Het
Napg C T 18: 63,127,375 (GRCm39) probably benign Het
Or1j11 T C 2: 36,312,156 (GRCm39) S249P possibly damaging Het
Or5k1 C T 16: 58,617,843 (GRCm39) R122H probably benign Het
Or7g33 A G 9: 19,449,142 (GRCm39) F28S possibly damaging Het
Or8d2 T C 9: 38,760,222 (GRCm39) S271P probably damaging Het
Pias1 T A 9: 62,830,926 (GRCm39) S161C probably damaging Het
Pias1 G T 9: 62,830,927 (GRCm39) N160K possibly damaging Het
Pigp G A 16: 94,168,466 (GRCm39) P37S probably damaging Het
Pik3c2b T A 1: 133,020,065 (GRCm39) V1070E probably benign Het
Pramel51 G T 12: 88,142,792 (GRCm39) H275Q probably benign Het
Prepl T C 17: 85,378,010 (GRCm39) T457A probably damaging Het
Psg23 G A 7: 18,340,853 (GRCm39) A467V probably benign Het
Rad54l T C 4: 115,980,146 (GRCm39) R13G probably benign Het
Rassf5 T C 1: 131,108,336 (GRCm39) D248G probably damaging Het
Rspo1 A G 4: 124,898,955 (GRCm39) N92S probably damaging Het
Scube1 G A 15: 83,543,217 (GRCm39) probably benign Het
Sec31b C A 19: 44,511,554 (GRCm39) V616F probably damaging Het
Sema3a T C 5: 13,615,881 (GRCm39) V435A probably damaging Het
Slc7a10 T A 7: 34,897,123 (GRCm39) I208N probably damaging Het
Stab2 A T 10: 86,692,420 (GRCm39) M2151K possibly damaging Het
Tacc1 T C 8: 25,665,235 (GRCm39) D50G probably damaging Het
Tas2r121 G T 6: 132,677,480 (GRCm39) T164N probably damaging Het
Tatdn2 T C 6: 113,681,676 (GRCm39) W570R probably damaging Het
Telo2 A T 17: 25,323,628 (GRCm39) F600I probably damaging Het
Trim36 T A 18: 46,305,669 (GRCm39) H426L probably benign Het
Trpm6 A T 19: 18,787,016 (GRCm39) N531Y possibly damaging Het
Ttc39a T C 4: 109,299,920 (GRCm39) C470R probably damaging Het
Ttn C T 2: 76,615,283 (GRCm39) E8485K probably damaging Het
Ubr4 A T 4: 139,196,122 (GRCm39) I1253F probably damaging Het
Unc79 A T 12: 103,088,688 (GRCm39) H1724L possibly damaging Het
Vmn1r40 T A 6: 89,691,998 (GRCm39) C89S probably benign Het
Wdr55 A G 18: 36,896,435 (GRCm39) E375G probably benign Het
Other mutations in Or9r3
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0472:Or9r3 UTSW 10 129,948,449 (GRCm39) missense probably damaging 1.00
R0609:Or9r3 UTSW 10 129,948,449 (GRCm39) missense probably damaging 1.00
R1619:Or9r3 UTSW 10 129,948,548 (GRCm39) missense possibly damaging 0.89
R1641:Or9r3 UTSW 10 129,947,872 (GRCm39) nonsense probably null
R2057:Or9r3 UTSW 10 129,947,859 (GRCm39) missense probably benign 0.00
R6049:Or9r3 UTSW 10 129,948,481 (GRCm39) missense probably benign 0.01
R6638:Or9r3 UTSW 10 129,947,739 (GRCm39) missense probably benign 0.04
R7291:Or9r3 UTSW 10 129,948,093 (GRCm39) missense probably benign 0.07
R7602:Or9r3 UTSW 10 129,948,179 (GRCm39) missense probably benign 0.00
R8167:Or9r3 UTSW 10 129,948,350 (GRCm39) missense probably damaging 1.00
R8815:Or9r3 UTSW 10 129,947,808 (GRCm39) missense probably damaging 0.98
R9169:Or9r3 UTSW 10 129,947,723 (GRCm39) missense probably benign 0.04
R9647:Or9r3 UTSW 10 129,948,029 (GRCm39) missense probably damaging 0.99
X0022:Or9r3 UTSW 10 129,948,576 (GRCm39) missense probably benign
Posted On 2015-04-16