Incidental Mutation 'IGL02932:Or5p70'
ID 364134
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or5p70
Ensembl Gene ENSMUSG00000110253
Gene Name olfactory receptor family 5 subfamily P member 70
Synonyms MOR204-37, Olfr495, GA_x6K02T2PBJ9-10725148-10726140
Accession Numbers
Essential gene? Probably non essential (E-score: 0.168) question?
Stock # IGL02932
Quality Score
Status
Chromosome 7
Chromosomal Location 107994329-107995321 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 107994720 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Serine at position 131 (N131S)
Ref Sequence ENSEMBL: ENSMUSP00000150689 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000210990] [ENSMUST00000215215]
AlphaFold Q8VF12
Predicted Effect probably benign
Transcript: ENSMUST00000210990
AA Change: N131S

PolyPhen 2 Score 0.025 (Sensitivity: 0.95; Specificity: 0.81)
Predicted Effect probably benign
Transcript: ENSMUST00000215215
AA Change: N131S

PolyPhen 2 Score 0.025 (Sensitivity: 0.95; Specificity: 0.81)
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: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgap42 T A 9: 9,115,709 (GRCm39) E122D probably damaging Het
Asb3 G A 11: 30,979,067 (GRCm39) probably null Het
Avl9 T C 6: 56,713,536 (GRCm39) S265P probably benign Het
Cep44 C T 8: 57,000,459 (GRCm39) R18Q probably damaging Het
Clec10a T C 11: 70,060,554 (GRCm39) probably benign Het
Cog4 A G 8: 111,579,065 (GRCm39) I115V probably benign Het
Coq3 C T 4: 21,900,430 (GRCm39) A219V probably benign Het
Cry2 G A 2: 92,243,462 (GRCm39) R460* probably null Het
Ddx39b A G 17: 35,472,337 (GRCm39) probably benign Het
Dhx40 G A 11: 86,662,755 (GRCm39) R646C probably damaging Het
Ears2 G A 7: 121,662,284 (GRCm39) R55C probably damaging Het
Eif3m C T 2: 104,845,214 (GRCm39) G26R probably damaging Het
Exo5 A G 4: 120,779,742 (GRCm39) L41P probably benign Het
Fut10 A G 8: 31,749,965 (GRCm39) H417R probably damaging Het
Gars1 T A 6: 55,037,929 (GRCm39) L296Q probably damaging Het
Gpr143 A T X: 151,576,439 (GRCm39) probably benign Het
Htr1b C A 9: 81,513,689 (GRCm39) R306L probably damaging Het
Lama3 G A 18: 12,661,858 (GRCm39) A2185T probably damaging Het
Mbd5 C A 2: 49,169,460 (GRCm39) Q1544K possibly damaging Het
Mccc1 T C 3: 36,014,178 (GRCm39) E713G possibly damaging Het
Mttp A G 3: 137,817,505 (GRCm39) F415S probably benign Het
Mug1 A G 6: 121,864,386 (GRCm39) T1428A probably benign Het
Mup6 A C 4: 60,006,009 (GRCm39) D159A probably damaging Het
Nsd2 T C 5: 34,037,472 (GRCm39) L698P probably damaging Het
Or2w6 A T 13: 21,843,001 (GRCm39) M164K probably damaging Het
Or4p22 G T 2: 88,317,519 (GRCm39) V148F probably benign Het
Or6c217 A T 10: 129,738,287 (GRCm39) C97* probably null Het
Osgepl1 G A 1: 53,360,675 (GRCm39) R372H probably benign Het
Pias2 C T 18: 77,232,799 (GRCm39) H537Y probably damaging Het
Slc38a7 A C 8: 96,572,783 (GRCm39) I149M probably damaging Het
Smn1 A G 13: 100,264,472 (GRCm39) T68A probably benign Het
Syde2 A G 3: 145,707,231 (GRCm39) K657R possibly damaging Het
Tdrd5 A T 1: 156,098,190 (GRCm39) H625Q possibly damaging Het
Tead3 T C 17: 28,560,325 (GRCm39) Y2C probably damaging Het
Tmem255a T A X: 37,296,940 (GRCm39) T280S probably benign Het
Ttpa A G 4: 20,021,215 (GRCm39) T128A possibly damaging Het
Wdhd1 A G 14: 47,509,591 (GRCm39) probably null Het
Other mutations in Or5p70
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01382:Or5p70 APN 7 107,994,452 (GRCm39) missense probably benign 0.31
IGL02430:Or5p70 APN 7 107,994,929 (GRCm39) missense probably benign 0.01
IGL02511:Or5p70 APN 7 107,995,265 (GRCm39) missense probably benign 0.06
IGL03222:Or5p70 APN 7 107,994,393 (GRCm39) missense possibly damaging 0.77
FR4340:Or5p70 UTSW 7 107,995,105 (GRCm39) missense probably benign
FR4340:Or5p70 UTSW 7 107,995,100 (GRCm39) missense probably benign
FR4342:Or5p70 UTSW 7 107,995,105 (GRCm39) missense probably benign
FR4342:Or5p70 UTSW 7 107,995,100 (GRCm39) missense probably benign
R0141:Or5p70 UTSW 7 107,994,575 (GRCm39) missense probably benign 0.06
R0600:Or5p70 UTSW 7 107,994,438 (GRCm39) missense probably damaging 0.98
R0635:Or5p70 UTSW 7 107,994,971 (GRCm39) missense probably benign 0.01
R0685:Or5p70 UTSW 7 107,994,470 (GRCm39) missense possibly damaging 0.67
R1220:Or5p70 UTSW 7 107,994,539 (GRCm39) missense probably benign 0.03
R1398:Or5p70 UTSW 7 107,994,708 (GRCm39) missense probably damaging 0.98
R1501:Or5p70 UTSW 7 107,995,289 (GRCm39) missense probably benign 0.00
R1990:Or5p70 UTSW 7 107,995,041 (GRCm39) missense probably benign 0.00
R2091:Or5p70 UTSW 7 107,995,068 (GRCm39) missense probably damaging 1.00
R2473:Or5p70 UTSW 7 107,994,711 (GRCm39) missense probably damaging 1.00
R3120:Or5p70 UTSW 7 107,994,930 (GRCm39) missense possibly damaging 0.67
R4771:Or5p70 UTSW 7 107,995,229 (GRCm39) nonsense probably null
R5240:Or5p70 UTSW 7 107,994,909 (GRCm39) missense probably damaging 0.99
R5510:Or5p70 UTSW 7 107,994,332 (GRCm39) missense probably benign 0.01
R5703:Or5p70 UTSW 7 107,994,707 (GRCm39) missense probably benign 0.23
R6102:Or5p70 UTSW 7 107,994,491 (GRCm39) missense probably damaging 0.99
R6110:Or5p70 UTSW 7 107,995,035 (GRCm39) missense possibly damaging 0.93
R6782:Or5p70 UTSW 7 107,994,744 (GRCm39) missense probably damaging 1.00
R7062:Or5p70 UTSW 7 107,995,037 (GRCm39) nonsense probably null
R7783:Or5p70 UTSW 7 107,995,296 (GRCm39) missense probably benign 0.15
R8386:Or5p70 UTSW 7 107,994,555 (GRCm39) small deletion probably benign
R9347:Or5p70 UTSW 7 107,995,259 (GRCm39) missense probably benign 0.02
R9468:Or5p70 UTSW 7 107,994,849 (GRCm39) missense possibly damaging 0.56
R9554:Or5p70 UTSW 7 107,994,365 (GRCm39) missense probably benign 0.03
Posted On 2015-12-18