Incidental Mutation 'IGL02897:Or51aa5'
ID 363446
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or51aa5
Ensembl Gene ENSMUSG00000096584
Gene Name olfactory receptor family 51 subfamily AA member 5
Synonyms MOR15-1, MOR15-4, Olfr611, GA_x6K02T2PBJ9-6236637-6235666
Accession Numbers
Essential gene? Probably non essential (E-score: 0.072) question?
Stock # IGL02897
Quality Score
Status
Chromosome 7
Chromosomal Location 103166618-103167589 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 103167337 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Glycine at position 85 (R85G)
Ref Sequence ENSEMBL: ENSMUSP00000149114 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000078108] [ENSMUST00000216074]
AlphaFold K7N609
Predicted Effect probably benign
Transcript: ENSMUST00000078108
AA Change: R85G

PolyPhen 2 Score 0.009 (Sensitivity: 0.96; Specificity: 0.77)
SMART Domains Protein: ENSMUSP00000077246
Gene: ENSMUSG00000096584
AA Change: R85G

DomainStartEndE-ValueType
Pfam:7tm_4 33 312 5.6e-110 PFAM
Pfam:7TM_GPCR_Srsx 37 309 4.6e-11 PFAM
Pfam:7tm_1 43 294 1e-19 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000216074
AA Change: R85G

PolyPhen 2 Score 0.009 (Sensitivity: 0.96; Specificity: 0.77)
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: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700093K21Rik T A 11: 23,467,308 (GRCm39) E108D probably benign Het
Abca7 T C 10: 79,837,426 (GRCm39) F437L probably damaging Het
Abi2 T C 1: 60,487,353 (GRCm39) V134A probably damaging Het
Ablim2 T C 5: 35,990,470 (GRCm39) I75T probably damaging Het
Aldh1a3 A G 7: 66,077,075 (GRCm39) V29A probably benign Het
Bptf T C 11: 106,937,947 (GRCm39) K2715E probably damaging Het
Cd163 A T 6: 124,302,486 (GRCm39) S1017C probably damaging Het
Cdc14b T C 13: 64,395,067 (GRCm39) I76V probably benign Het
Cers6 T A 2: 68,764,877 (GRCm39) C63* probably null Het
Chd9 T C 8: 91,660,496 (GRCm39) probably benign Het
Col19a1 T C 1: 24,573,179 (GRCm39) N198D unknown Het
Cse1l T C 2: 166,761,628 (GRCm39) C61R possibly damaging Het
Cubn T C 2: 13,323,123 (GRCm39) T2815A possibly damaging Het
Cyp19a1 G T 9: 54,074,195 (GRCm39) T453K possibly damaging Het
Dlg1 G T 16: 31,590,674 (GRCm39) probably null Het
Dpp7 T C 2: 25,243,684 (GRCm39) Y339C probably damaging Het
Dtl T C 1: 191,273,656 (GRCm39) probably benign Het
Gm5591 T C 7: 38,219,466 (GRCm39) E469G probably damaging Het
Ing3 T A 6: 21,969,325 (GRCm39) V202E probably benign Het
Inpp5j A G 11: 3,450,619 (GRCm39) L578P probably damaging Het
Irak4 A G 15: 94,451,872 (GRCm39) N155S probably benign Het
Kif2b A T 11: 91,467,045 (GRCm39) S413T probably damaging Het
L3mbtl1 A T 2: 162,807,692 (GRCm39) Y490F probably damaging Het
Med17 T G 9: 15,178,830 (GRCm39) D447A probably damaging Het
Med26 T C 8: 73,250,365 (GRCm39) T245A probably benign Het
Nlrc3 A T 16: 3,781,938 (GRCm39) S490R possibly damaging Het
Nme5 A G 18: 34,702,956 (GRCm39) probably benign Het
Rnf10 G T 5: 115,386,700 (GRCm39) Q530K probably benign Het
Robo3 A T 9: 37,338,798 (GRCm39) Y281* probably null Het
Sclt1 T C 3: 41,629,822 (GRCm39) I330V probably benign Het
Smim14 A T 5: 65,607,739 (GRCm39) probably benign Het
Trank1 T G 9: 111,196,585 (GRCm39) H1536Q probably damaging Het
Tspan18 A G 2: 93,050,518 (GRCm39) L35P possibly damaging Het
Ubr4 G A 4: 139,199,819 (GRCm39) V4568M probably damaging Het
Vmn1r63 A G 7: 5,805,744 (GRCm39) V296A possibly damaging Het
Other mutations in Or51aa5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01707:Or51aa5 APN 7 103,167,141 (GRCm39) missense probably damaging 1.00
IGL01950:Or51aa5 APN 7 103,167,472 (GRCm39) missense probably benign 0.34
IGL02968:Or51aa5 APN 7 103,167,466 (GRCm39) missense probably damaging 0.99
R0167:Or51aa5 UTSW 7 103,166,708 (GRCm39) nonsense probably null
R0739:Or51aa5 UTSW 7 103,166,931 (GRCm39) missense probably damaging 1.00
R2992:Or51aa5 UTSW 7 103,166,977 (GRCm39) missense probably damaging 0.98
R4094:Or51aa5 UTSW 7 103,167,244 (GRCm39) missense possibly damaging 0.93
R4451:Or51aa5 UTSW 7 103,167,184 (GRCm39) missense probably damaging 1.00
R4735:Or51aa5 UTSW 7 103,167,030 (GRCm39) missense possibly damaging 0.89
R7585:Or51aa5 UTSW 7 103,167,166 (GRCm39) missense possibly damaging 0.50
R8921:Or51aa5 UTSW 7 103,167,030 (GRCm39) missense possibly damaging 0.89
R9505:Or51aa5 UTSW 7 103,167,446 (GRCm39) missense probably benign 0.03
Posted On 2015-12-18