Incidental Mutation 'IGL02122:Or5w10'
ID 280658
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or5w10
Ensembl Gene ENSMUSG00000075156
Gene Name olfactory receptor family 5 subfamily W member 10
Synonyms MOR176-3, Olfr1128, GA_x6K02T2Q125-49048592-49047657
Accession Numbers
Essential gene? Probably non essential (E-score: 0.055) question?
Stock # IGL02122
Quality Score
Status
Chromosome 2
Chromosomal Location 87374951-87375886 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 87375447 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 147 (V147A)
Ref Sequence ENSEMBL: ENSMUSP00000099684 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000102624]
AlphaFold Q7TR47
Predicted Effect probably benign
Transcript: ENSMUST00000102624
AA Change: V147A

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
SMART Domains Protein: ENSMUSP00000099684
Gene: ENSMUSG00000075156
AA Change: V147A

DomainStartEndE-ValueType
Pfam:7tm_4 31 307 5.3e-46 PFAM
Pfam:7tm_1 41 290 3.2e-16 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000120590
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: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700049A03Rik C T 12: 71,217,299 (GRCm39) T756I possibly damaging Het
Abi3bp T C 16: 56,507,491 (GRCm39) probably benign Het
Adcy5 G A 16: 35,103,982 (GRCm39) probably benign Het
Adcy6 T A 15: 98,496,763 (GRCm39) H504L possibly damaging Het
Ank2 A G 3: 126,731,523 (GRCm39) probably benign Het
Atxn2 A G 5: 121,916,093 (GRCm39) D34G probably damaging Het
Brd8 C T 18: 34,735,780 (GRCm39) S899N probably damaging Het
Carmil1 T C 13: 24,220,541 (GRCm39) E657G possibly damaging Het
Cdc25c T C 18: 34,877,038 (GRCm39) I212V probably benign Het
Chl1 A G 6: 103,652,098 (GRCm39) D338G probably benign Het
Cog6 T C 3: 52,905,763 (GRCm39) I361V probably benign Het
Dip2c T C 13: 9,556,695 (GRCm39) S80P possibly damaging Het
Dmrtc2 A T 7: 24,572,008 (GRCm39) R34S possibly damaging Het
Exph5 A G 9: 53,284,974 (GRCm39) N685S probably benign Het
Flnc A T 6: 29,444,335 (GRCm39) I684L possibly damaging Het
Foxk1 T A 5: 142,437,184 (GRCm39) probably benign Het
Gprc6a T C 10: 51,502,819 (GRCm39) N348S probably benign Het
Gspt1 T C 16: 11,047,080 (GRCm39) K445R probably damaging Het
Hace1 T C 10: 45,494,700 (GRCm39) V170A probably damaging Het
Hydin T C 8: 111,221,047 (GRCm39) I1481T possibly damaging Het
Ighv4-1 A T 12: 113,912,145 (GRCm39) L36Q possibly damaging Het
Ints1 G A 5: 139,750,905 (GRCm39) Q833* probably null Het
Myo15a T C 11: 60,374,292 (GRCm39) F96L probably benign Het
Myom1 G T 17: 71,399,132 (GRCm39) R998L probably damaging Het
Nacc2 A G 2: 25,979,960 (GRCm39) S159P probably benign Het
Or5k15 T C 16: 58,710,134 (GRCm39) T150A probably benign Het
Or7e177 T A 9: 20,211,880 (GRCm39) L128Q probably damaging Het
Pbrm1 A G 14: 30,811,573 (GRCm39) I1197V probably damaging Het
Pde4dip G A 3: 97,674,737 (GRCm39) R60C probably damaging Het
Pfkfb4 C T 9: 108,854,178 (GRCm39) R351W probably damaging Het
Pitpnm1 T C 19: 4,157,796 (GRCm39) Y499H probably damaging Het
Plekhn1 C T 4: 156,308,313 (GRCm39) probably null Het
Prmt8 A G 6: 127,667,680 (GRCm39) Y332H probably benign Het
Prpf38a A G 4: 108,436,238 (GRCm39) I25T possibly damaging Het
Rpf1 T C 3: 146,227,022 (GRCm39) K44E probably benign Het
Rusc2 T C 4: 43,421,685 (GRCm39) F702L possibly damaging Het
Ryr2 A T 13: 11,756,755 (GRCm39) I1633K probably damaging Het
Slc39a10 G A 1: 46,857,288 (GRCm39) A696V probably damaging Het
Tkt T C 14: 30,293,158 (GRCm39) V510A possibly damaging Het
Tmem106a C A 11: 101,481,240 (GRCm39) N249K probably damaging Het
Tmpo A T 10: 90,999,998 (GRCm39) S157T possibly damaging Het
Tspan32 A T 7: 142,569,372 (GRCm39) I144F probably damaging Het
Ufsp2 G A 8: 46,448,685 (GRCm39) V429I probably benign Het
Unc13c T A 9: 73,641,679 (GRCm39) probably benign Het
Usp47 A T 7: 111,706,115 (GRCm39) K1259M probably damaging Het
Zdhhc18 A T 4: 133,340,946 (GRCm39) probably benign Het
Zfp507 G T 7: 35,475,520 (GRCm39) L898I probably damaging Het
Other mutations in Or5w10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02638:Or5w10 APN 2 87,375,093 (GRCm39) missense probably damaging 1.00
IGL02749:Or5w10 APN 2 87,375,001 (GRCm39) missense probably damaging 1.00
R1650:Or5w10 UTSW 2 87,375,772 (GRCm39) missense probably benign 0.01
R1789:Or5w10 UTSW 2 87,375,327 (GRCm39) missense probably damaging 1.00
R2100:Or5w10 UTSW 2 87,375,169 (GRCm39) missense probably damaging 1.00
R2163:Or5w10 UTSW 2 87,375,238 (GRCm39) missense probably damaging 1.00
R3950:Or5w10 UTSW 2 87,375,409 (GRCm39) missense probably damaging 1.00
R3951:Or5w10 UTSW 2 87,375,409 (GRCm39) missense probably damaging 1.00
R3952:Or5w10 UTSW 2 87,375,409 (GRCm39) missense probably damaging 1.00
R6185:Or5w10 UTSW 2 87,375,087 (GRCm39) missense possibly damaging 0.87
R8493:Or5w10 UTSW 2 87,375,114 (GRCm39) missense probably damaging 1.00
R8869:Or5w10 UTSW 2 87,375,753 (GRCm39) missense probably damaging 1.00
Z1176:Or5w10 UTSW 2 87,374,965 (GRCm39) missense probably benign 0.00
Posted On 2015-04-16