Incidental Mutation 'IGL01615:Or5p55'
ID 92341
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or5p55
Ensembl Gene ENSMUSG00000095301
Gene Name olfactory receptor family 5 subfamily P member 55
Synonyms GA_x6K02T2PBJ9-10296787-10297719, Olfr476, MOR204-3
Accession Numbers
Essential gene? Probably non essential (E-score: 0.056) question?
Stock # IGL01615
Quality Score
Status
Chromosome 7
Chromosomal Location 107566606-107567538 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 107567144 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 180 (D180G)
Ref Sequence ENSEMBL: ENSMUSP00000149760 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000077249] [ENSMUST00000217173]
AlphaFold Q8VGI4
Predicted Effect probably damaging
Transcript: ENSMUST00000077249
AA Change: D180G

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
SMART Domains Protein: ENSMUSP00000076485
Gene: ENSMUSG00000095301
AA Change: D180G

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 1.7e-51 PFAM
Pfam:7tm_1 41 290 4.1e-19 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000217173
AA Change: D180G

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
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: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adnp2 T C 18: 80,171,692 (GRCm39) T906A probably damaging Het
Akap13 A G 7: 75,347,141 (GRCm39) S1731G probably damaging Het
Apbb2 A G 5: 66,465,044 (GRCm39) V650A probably benign Het
Appl1 A G 14: 26,681,427 (GRCm39) probably benign Het
Avpr1b T G 1: 131,527,885 (GRCm39) V136G probably damaging Het
C6 T C 15: 4,811,378 (GRCm39) F409L probably benign Het
Ccdc121rt3 A G 5: 112,503,696 (GRCm39) S3P possibly damaging Het
Cdk20 A G 13: 64,584,124 (GRCm39) probably benign Het
Cenpf T C 1: 189,385,381 (GRCm39) K2300E possibly damaging Het
Cfap57 C T 4: 118,457,993 (GRCm39) R399Q probably damaging Het
Cimap3 G T 3: 105,904,523 (GRCm39) probably null Het
Cnnm1 A T 19: 43,460,375 (GRCm39) S706C probably benign Het
Cr1l T C 1: 194,812,189 (GRCm39) I45V possibly damaging Het
D130043K22Rik A T 13: 25,083,779 (GRCm39) R1081S probably damaging Het
Ddx60 A T 8: 62,416,774 (GRCm39) H573L probably null Het
Eif5b T C 1: 38,084,787 (GRCm39) L878S probably damaging Het
Ets1 T C 9: 32,644,235 (GRCm39) probably benign Het
Evi5 A G 5: 107,912,573 (GRCm39) L696P probably damaging Het
Fbh1 C A 2: 11,762,334 (GRCm39) E12* probably null Het
Gabpb1 C A 2: 126,495,520 (GRCm39) M77I possibly damaging Het
Glul T A 1: 153,782,222 (GRCm39) N152K probably benign Het
Gm45234 T C 6: 124,723,394 (GRCm39) Y613C probably damaging Het
Gm5611 A G 9: 16,941,647 (GRCm39) noncoding transcript Het
Gpr156 T A 16: 37,808,953 (GRCm39) I225K probably damaging Het
Herc4 T C 10: 63,126,461 (GRCm39) probably benign Het
Iqsec3 C T 6: 121,387,580 (GRCm39) V720M probably damaging Het
Itgam A T 7: 127,715,939 (GRCm39) H1104L possibly damaging Het
Itgb3 T A 11: 104,534,791 (GRCm39) D549E probably damaging Het
Kctd7 A T 5: 130,176,976 (GRCm39) M76L probably damaging Het
Kdm3b T G 18: 34,962,284 (GRCm39) N1523K probably damaging Het
Map3k12 T A 15: 102,412,186 (GRCm39) E318D probably damaging Het
Mc1r T C 8: 124,134,789 (GRCm39) Y181H probably damaging Het
Mex3c G A 18: 73,706,703 (GRCm39) A197T unknown Het
Mvk A G 5: 114,584,353 (GRCm39) D71G probably benign Het
Ndufb3 T A 1: 58,634,912 (GRCm39) L88* probably null Het
Or56a4 A G 7: 104,806,667 (GRCm39) V74A probably benign Het
Pramel17 T A 4: 101,694,201 (GRCm39) R227S possibly damaging Het
Psmg2 G A 18: 67,786,293 (GRCm39) V218I probably benign Het
Slc5a3 C T 16: 91,876,000 (GRCm39) Q686* probably null Het
Vmn2r75 T C 7: 85,797,681 (GRCm39) I711V probably benign Het
Vps13c T A 9: 67,863,063 (GRCm39) H3026Q probably benign Het
Zfp354c A G 11: 50,708,732 (GRCm39) S22P possibly damaging Het
Other mutations in Or5p55
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01063:Or5p55 APN 7 107,566,741 (GRCm39) missense probably damaging 1.00
IGL01403:Or5p55 APN 7 107,566,828 (GRCm39) missense possibly damaging 0.64
IGL01564:Or5p55 APN 7 107,567,198 (GRCm39) missense probably benign 0.11
IGL01777:Or5p55 APN 7 107,566,709 (GRCm39) missense probably damaging 1.00
IGL01999:Or5p55 APN 7 107,566,675 (GRCm39) missense probably benign
IGL02239:Or5p55 APN 7 107,567,254 (GRCm39) missense probably damaging 1.00
R0636:Or5p55 UTSW 7 107,566,679 (GRCm39) missense probably benign 0.00
R1986:Or5p55 UTSW 7 107,566,877 (GRCm39) missense probably benign
R5109:Or5p55 UTSW 7 107,567,104 (GRCm39) missense probably benign 0.06
R6363:Or5p55 UTSW 7 107,566,957 (GRCm39) missense possibly damaging 0.57
R6526:Or5p55 UTSW 7 107,566,669 (GRCm39) missense probably benign 0.03
R6907:Or5p55 UTSW 7 107,567,459 (GRCm39) missense probably damaging 1.00
R7063:Or5p55 UTSW 7 107,567,411 (GRCm39) missense probably benign
R7218:Or5p55 UTSW 7 107,566,874 (GRCm39) missense probably benign
R7240:Or5p55 UTSW 7 107,567,395 (GRCm39) missense probably benign 0.42
R7444:Or5p55 UTSW 7 107,566,811 (GRCm39) missense probably damaging 0.99
R7939:Or5p55 UTSW 7 107,566,986 (GRCm39) nonsense probably null
R8060:Or5p55 UTSW 7 107,566,612 (GRCm39) missense probably benign
R8953:Or5p55 UTSW 7 107,567,251 (GRCm39) missense probably benign 0.00
R9159:Or5p55 UTSW 7 107,567,524 (GRCm39) nonsense probably null
R9438:Or5p55 UTSW 7 107,567,000 (GRCm39) missense probably damaging 1.00
X0025:Or5p55 UTSW 7 107,567,395 (GRCm39) missense possibly damaging 0.75
Posted On 2013-12-09