Incidental Mutation 'IGL00329:Olfr651'
ID5183
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Olfr651
Ensembl Gene ENSMUSG00000073928
Gene Nameolfactory receptor 651
SynonymsGA_x6K02T2PBJ9-7179540-7180481, MOR31-11
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.076) question?
Stock #IGL00329
Quality Score
Status
Chromosome7
Chromosomal Location104550133-104554422 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to A at 104553092 bp
ZygosityHeterozygous
Amino Acid Change Proline to Threonine at position 58 (P58T)
Ref Sequence ENSEMBL: ENSMUSP00000150776 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000098176] [ENSMUST00000216904]
Predicted Effect probably benign
Transcript: ENSMUST00000098176
AA Change: P58T

PolyPhen 2 Score 0.177 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000095778
Gene: ENSMUSG00000073928
AA Change: P58T

DomainStartEndE-ValueType
Pfam:7tm_4 31 310 4.1e-104 PFAM
Pfam:7TM_GPCR_Srsx 35 303 1e-10 PFAM
Pfam:7tm_1 41 292 4.1e-19 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000216246
Predicted Effect probably benign
Transcript: ENSMUST00000216904
AA Change: P58T

PolyPhen 2 Score 0.177 (Sensitivity: 0.92; Specificity: 0.87)
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: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2010111I01Rik T A 13: 63,191,163 I623N probably damaging Het
Acad9 A G 3: 36,069,762 N72S probably benign Het
Apba3 C T 10: 81,273,067 P555S probably damaging Het
Arcn1 C A 9: 44,759,036 E98* probably null Het
Col28a1 G T 6: 8,175,425 T141K probably damaging Het
Dna2 T C 10: 62,966,443 F811S probably damaging Het
Dusp19 T A 2: 80,630,925 I186K probably damaging Het
Dync2li1 A G 17: 84,644,726 D195G possibly damaging Het
Epm2aip1 T C 9: 111,272,787 V276A possibly damaging Het
Extl3 T C 14: 65,075,621 E704G probably benign Het
Fam166b G A 4: 43,428,158 R100W possibly damaging Het
Gle1 T C 2: 29,939,289 probably benign Het
Gm2178 C A 14: 26,514,612 probably benign Het
Gm4553 T C 7: 142,165,227 S155G unknown Het
Gm7257 G A 9: 36,432,902 probably benign Het
Herc2 T A 7: 56,124,299 L1166Q probably damaging Het
Hsd11b2 A G 8: 105,523,127 E290G probably benign Het
Inpp5d T C 1: 87,668,003 V157A probably benign Het
Krt72 T A 15: 101,784,999 Q160L probably damaging Het
Lrrd1 A G 5: 3,850,081 K129E possibly damaging Het
Mapk13 A G 17: 28,776,405 Y200C probably damaging Het
Mme G A 3: 63,380,328 W750* probably null Het
Nat8l C T 5: 33,998,417 P139L probably damaging Het
Nrtn C A 17: 56,751,569 R144L probably benign Het
Pdgfa T A 5: 138,988,461 probably benign Het
Rtp3 A G 9: 110,986,598 V233A probably benign Het
Syne2 A G 12: 76,031,700 probably benign Het
Trappc10 A T 10: 78,203,877 probably benign Het
Usp24 A G 4: 106,359,091 T380A probably benign Het
Vmn1r21 A T 6: 57,844,064 S132T probably benign Het
Other mutations in Olfr651
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01120:Olfr651 APN 7 104553345 missense probably benign
IGL01325:Olfr651 APN 7 104553689 missense probably damaging 1.00
IGL01590:Olfr651 APN 7 104553575 missense probably benign 0.00
IGL02625:Olfr651 APN 7 104553573 missense probably damaging 1.00
IGL02685:Olfr651 APN 7 104553150 missense probably benign 0.35
P0157:Olfr651 UTSW 7 104553507 missense probably damaging 1.00
R0087:Olfr651 UTSW 7 104553662 missense possibly damaging 0.73
R0399:Olfr651 UTSW 7 104553369 missense probably benign 0.05
R0547:Olfr651 UTSW 7 104553356 missense probably benign 0.01
R0630:Olfr651 UTSW 7 104553791 missense probably benign 0.27
R1014:Olfr651 UTSW 7 104553176 missense probably damaging 1.00
R1127:Olfr651 UTSW 7 104553086 missense possibly damaging 0.94
R1724:Olfr651 UTSW 7 104553228 missense probably damaging 1.00
R2473:Olfr651 UTSW 7 104552939 missense possibly damaging 0.93
R3115:Olfr651 UTSW 7 104553088 missense probably benign 0.13
R3116:Olfr651 UTSW 7 104553088 missense probably benign 0.13
R3834:Olfr651 UTSW 7 104553345 missense probably benign 0.43
R4027:Olfr651 UTSW 7 104553323 missense possibly damaging 0.90
R4423:Olfr651 UTSW 7 104553345 missense probably benign
R4907:Olfr651 UTSW 7 104553311 missense probably damaging 0.97
R4984:Olfr651 UTSW 7 104553021 missense probably benign 0.38
R5266:Olfr651 UTSW 7 104553819 missense probably benign 0.00
R5592:Olfr651 UTSW 7 104553731 missense probably benign 0.28
R6441:Olfr651 UTSW 7 104553335 nonsense probably null
R7463:Olfr651 UTSW 7 104553482 missense possibly damaging 0.88
R7647:Olfr651 UTSW 7 104553686 missense probably benign 0.00
R8276:Olfr651 UTSW 7 104553315 missense probably damaging 1.00
X0067:Olfr651 UTSW 7 104553387 missense probably damaging 0.97
Posted On2012-04-20