Incidental Mutation 'IGL03008:Or5p79'
ID 407626
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or5p79
Ensembl Gene ENSMUSG00000061000
Gene Name olfactory receptor family 5 subfamily P member 79
Synonyms Olfr507, GA_x6K02T2PBJ9-10951546-10952496, MOR204-7
Accession Numbers
Essential gene? Probably non essential (E-score: 0.139) question?
Stock # IGL03008
Quality Score
Status
Chromosome 7
Chromosomal Location 108221021-108221971 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 108221490 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Arginine at position 157 (L157R)
Ref Sequence ENSEMBL: ENSMUSP00000078926 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080014]
AlphaFold Q8VG13
Predicted Effect probably damaging
Transcript: ENSMUST00000080014
AA Change: L157R

PolyPhen 2 Score 0.986 (Sensitivity: 0.74; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000078926
Gene: ENSMUSG00000061000
AA Change: L157R

DomainStartEndE-ValueType
Pfam:7tm_4 34 313 6.1e-52 PFAM
Pfam:7tm_1 44 295 1e-20 PFAM
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: 70 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aga T C 8: 53,964,861 (GRCm39) S8P probably benign Het
Ankrd34c C T 9: 89,612,337 (GRCm39) M1I probably null Het
Ankrd44 T C 1: 54,805,968 (GRCm39) H146R probably damaging Het
Bst1 A G 5: 43,983,604 (GRCm39) probably null Het
Btbd8 T G 5: 107,639,464 (GRCm39) probably null Het
Cdh12 A T 15: 21,480,416 (GRCm39) I211F probably damaging Het
Cenpj G T 14: 56,764,406 (GRCm39) D1335E probably benign Het
Clpx G A 9: 65,230,057 (GRCm39) V502I possibly damaging Het
Cntnap4 T C 8: 113,500,222 (GRCm39) S505P probably benign Het
Cog2 T C 8: 125,262,131 (GRCm39) probably benign Het
Cped1 A G 6: 22,233,601 (GRCm39) Q819R probably benign Het
Cspg4 A G 9: 56,805,759 (GRCm39) E2190G possibly damaging Het
Ctsa G A 2: 164,679,368 (GRCm39) R359Q probably damaging Het
Cul9 A G 17: 46,813,623 (GRCm39) probably benign Het
Dab1 G T 4: 104,584,777 (GRCm39) V306F probably damaging Het
Dysf A G 6: 84,050,876 (GRCm39) I438V probably benign Het
Eif4g3 G T 4: 137,847,699 (GRCm39) G380W probably damaging Het
Exd1 T A 2: 119,350,862 (GRCm39) K466N probably benign Het
Eya3 A C 4: 132,434,294 (GRCm39) D325A probably damaging Het
Fmn1 A G 2: 113,195,445 (GRCm39) T382A unknown Het
Fry T A 5: 150,269,021 (GRCm39) D106E possibly damaging Het
Gm21957 T A 7: 124,818,733 (GRCm39) noncoding transcript Het
Gm44511 A G 6: 128,761,059 (GRCm39) probably benign Het
Itga4 A G 2: 79,155,982 (GRCm39) I983V probably benign Het
Lrpprc A T 17: 85,058,675 (GRCm39) D5E probably benign Het
Lrrc37 T C 11: 103,511,293 (GRCm39) E225G unknown Het
Ltbp4 G T 7: 27,023,789 (GRCm39) N747K probably damaging Het
Minar1 A G 9: 89,478,731 (GRCm39) Y772H probably damaging Het
Mlh3 T C 12: 85,287,625 (GRCm39) Q1308R probably benign Het
Mtfr2 T A 10: 20,229,185 (GRCm39) C63S possibly damaging Het
Myh11 T A 16: 14,022,617 (GRCm39) M1661L probably benign Het
Myo1c T C 11: 75,549,240 (GRCm39) M137T probably benign Het
Myocd A C 11: 65,078,392 (GRCm39) L340V probably damaging Het
Napsa A T 7: 44,235,220 (GRCm39) Q335L possibly damaging Het
Nlrp4b C A 7: 10,448,516 (GRCm39) Q240K probably benign Het
Npepps A C 11: 97,128,984 (GRCm39) F400C probably damaging Het
Nxpe4 A T 9: 48,304,738 (GRCm39) E275V probably benign Het
Ofd1 T C X: 165,192,530 (GRCm39) D501G probably benign Het
Or13a19 T C 7: 139,903,445 (GRCm39) Y278H probably damaging Het
Or4f6 A G 2: 111,838,868 (GRCm39) I221T possibly damaging Het
Or8k41 A T 2: 86,313,678 (GRCm39) M136K probably damaging Het
P2ry1 A T 3: 60,910,947 (GRCm39) T29S probably benign Het
Papss1 T C 3: 131,290,860 (GRCm39) V201A possibly damaging Het
Paxip1 A G 5: 27,957,764 (GRCm39) V864A probably benign Het
Pcdhgc5 T A 18: 37,954,887 (GRCm39) H720Q probably benign Het
Pdxdc1 T C 16: 13,694,023 (GRCm39) N133S possibly damaging Het
Prkar1a T C 11: 109,544,690 (GRCm39) I27T probably damaging Het
Rnf10 G T 5: 115,389,355 (GRCm39) H271N possibly damaging Het
Scn9a A G 2: 66,392,855 (GRCm39) S246P probably damaging Het
Sertad2 G T 11: 20,597,798 (GRCm39) probably benign Het
Slc22a27 A G 19: 7,887,067 (GRCm39) I274T possibly damaging Het
Slc22a5 A T 11: 53,782,058 (GRCm39) V103E probably damaging Het
Slc5a9 A T 4: 111,748,138 (GRCm39) F225I probably benign Het
Slc6a3 G A 13: 73,706,404 (GRCm39) probably null Het
Smcr8 A G 11: 60,669,287 (GRCm39) E145G probably damaging Het
Spen A T 4: 141,203,448 (GRCm39) D1726E possibly damaging Het
Sphkap A T 1: 83,254,552 (GRCm39) S779T probably damaging Het
Stag1 A T 9: 100,658,844 (GRCm39) N144Y probably damaging Het
Strada T C 11: 106,061,783 (GRCm39) H156R probably damaging Het
Stxbp2 A T 8: 3,691,971 (GRCm39) I538F probably benign Het
Tas2r138 A C 6: 40,590,116 (GRCm39) D43E probably damaging Het
Tdpoz3 A T 3: 93,733,642 (GRCm39) K106* probably null Het
Trbv13-1 A G 6: 41,093,229 (GRCm39) D54G probably damaging Het
Ttc39b A G 4: 83,165,932 (GRCm39) V218A probably benign Het
Ttn G A 2: 76,611,203 (GRCm39) T15697I probably damaging Het
Ugt2b38 G A 5: 87,560,282 (GRCm39) T344I probably benign Het
Vmn2r94 T C 17: 18,477,908 (GRCm39) M168V probably benign Het
Wdr11 T C 7: 129,208,715 (GRCm39) probably benign Het
Wipf2 T C 11: 98,783,554 (GRCm39) probably benign Het
Zranb2 T A 3: 157,252,302 (GRCm39) probably null Het
Other mutations in Or5p79
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01066:Or5p79 APN 7 108,221,064 (GRCm39) missense probably damaging 1.00
IGL01979:Or5p79 APN 7 108,221,648 (GRCm39) missense probably benign 0.09
IGL02373:Or5p79 APN 7 108,221,310 (GRCm39) missense probably benign 0.11
IGL02754:Or5p79 APN 7 108,221,880 (GRCm39) missense possibly damaging 0.94
R0305:Or5p79 UTSW 7 108,221,792 (GRCm39) missense probably benign 0.01
R0584:Or5p79 UTSW 7 108,221,622 (GRCm39) missense probably benign 0.00
R0611:Or5p79 UTSW 7 108,221,494 (GRCm39) missense possibly damaging 0.72
R0947:Or5p79 UTSW 7 108,221,879 (GRCm39) missense probably benign 0.02
R1488:Or5p79 UTSW 7 108,221,696 (GRCm39) missense probably damaging 1.00
R1808:Or5p79 UTSW 7 108,221,817 (GRCm39) missense possibly damaging 0.87
R3763:Or5p79 UTSW 7 108,221,924 (GRCm39) missense probably damaging 1.00
R4367:Or5p79 UTSW 7 108,221,096 (GRCm39) missense probably benign 0.27
R4369:Or5p79 UTSW 7 108,221,096 (GRCm39) missense probably benign 0.27
R4371:Or5p79 UTSW 7 108,221,096 (GRCm39) missense probably benign 0.27
R4609:Or5p79 UTSW 7 108,221,711 (GRCm39) missense probably benign 0.35
R5389:Or5p79 UTSW 7 108,221,924 (GRCm39) missense probably damaging 1.00
R6499:Or5p79 UTSW 7 108,221,713 (GRCm39) missense probably benign 0.02
R6684:Or5p79 UTSW 7 108,221,141 (GRCm39) missense probably damaging 0.98
R7531:Or5p79 UTSW 7 108,221,269 (GRCm39) missense probably benign 0.06
R7555:Or5p79 UTSW 7 108,221,933 (GRCm39) missense probably damaging 1.00
R7893:Or5p79 UTSW 7 108,221,844 (GRCm39) missense probably damaging 1.00
R8415:Or5p79 UTSW 7 108,221,163 (GRCm39) missense probably damaging 1.00
R8444:Or5p79 UTSW 7 108,221,027 (GRCm39) missense probably benign 0.00
R8904:Or5p79 UTSW 7 108,221,919 (GRCm39) missense probably damaging 0.98
R9635:Or5p79 UTSW 7 108,221,654 (GRCm39) missense probably benign 0.00
R9795:Or5p79 UTSW 7 108,221,869 (GRCm39) missense probably benign 0.39
Posted On 2016-08-02