Incidental Mutation 'IGL02613:Or5p56'
ID 300540
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or5p56
Ensembl Gene ENSMUSG00000096151
Gene Name olfactory receptor family 5 subfamily P member 56
Synonyms Olfr477, GA_x6K02T2PBJ9-10319672-10320604, MOR204-1
Accession Numbers
Essential gene? Probably non essential (E-score: 0.128) question?
Stock # IGL02613
Quality Score
Status
Chromosome 7
Chromosomal Location 107589574-107590506 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to T at 107590381 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Stop codon at position 270 (Q270*)
Ref Sequence ENSEMBL: ENSMUSP00000150605 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000091605] [ENSMUST00000214677]
AlphaFold Q8VGI6
Predicted Effect probably null
Transcript: ENSMUST00000091605
AA Change: Q270*
SMART Domains Protein: ENSMUSP00000091654
Gene: ENSMUSG00000096151
AA Change: Q270*

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 8e-52 PFAM
Pfam:7tm_1 41 290 1.9e-18 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000214677
AA Change: Q270*
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
Adcy8 T G 15: 64,655,833 (GRCm39) I549L possibly damaging Het
Arhgef17 A T 7: 100,578,103 (GRCm39) H948Q probably damaging Het
Auh A G 13: 53,073,035 (GRCm39) probably null Het
Btf3 A G 13: 98,446,714 (GRCm39) probably benign Het
Capg A G 6: 72,532,594 (GRCm39) N53S probably damaging Het
Cfap70 T C 14: 20,459,132 (GRCm39) probably null Het
Chrna5 A T 9: 54,913,705 (GRCm39) E417V probably damaging Het
Coch A G 12: 51,642,132 (GRCm39) T35A possibly damaging Het
Dock4 T A 12: 40,860,465 (GRCm39) L1284M probably damaging Het
Etv3 A G 3: 87,443,702 (GRCm39) T429A possibly damaging Het
Fmnl2 T C 2: 52,963,747 (GRCm39) probably null Het
Glb1 A G 9: 114,293,130 (GRCm39) T502A possibly damaging Het
Greb1 C A 12: 16,789,889 (GRCm39) probably null Het
Hspg2 A G 4: 137,271,731 (GRCm39) Y2499C probably damaging Het
Kcnq1 A T 7: 142,979,863 (GRCm39) probably benign Het
Lrriq1 A G 10: 102,980,409 (GRCm39) S1497P probably damaging Het
Magel2 G A 7: 62,029,946 (GRCm39) R950H unknown Het
Mcc A G 18: 44,563,021 (GRCm39) L982P probably damaging Het
Naif1 T A 2: 32,345,172 (GRCm39) M292K possibly damaging Het
Npb T A 11: 120,499,716 (GRCm39) C99S probably damaging Het
Obscn G T 11: 58,892,958 (GRCm39) R6763S probably benign Het
Or13a21 A G 7: 139,999,383 (GRCm39) V101A probably benign Het
Pip5k1c C A 10: 81,153,155 (GRCm39) probably null Het
Pitpnm3 A T 11: 71,948,898 (GRCm39) S736T probably damaging Het
Polr1a A T 6: 71,944,304 (GRCm39) E1257V probably damaging Het
Sec63 G A 10: 42,677,703 (GRCm39) D270N probably damaging Het
Snrnp200 C T 2: 127,060,346 (GRCm39) T530I probably damaging Het
Sorbs1 A T 19: 40,315,991 (GRCm39) N383K probably damaging Het
Syk G A 13: 52,797,076 (GRCm39) G546R probably damaging Het
Tfap2d T A 1: 19,189,415 (GRCm39) L265Q probably damaging Het
Trav12-1 C T 14: 53,775,742 (GRCm39) S9L possibly damaging Het
Trerf1 T C 17: 47,659,766 (GRCm39) noncoding transcript Het
Ttn T A 2: 76,558,704 (GRCm39) I29726L possibly damaging Het
Usp18 A G 6: 121,238,049 (GRCm39) T143A probably benign Het
Usp32 A T 11: 84,930,896 (GRCm39) N511K probably damaging Het
Wdr64 C T 1: 175,594,613 (GRCm39) Q4* probably null Het
Zfp277 A G 12: 40,379,514 (GRCm39) F340S probably damaging Het
Other mutations in Or5p56
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00907:Or5p56 APN 7 107,590,097 (GRCm39) missense probably damaging 0.97
IGL01078:Or5p56 APN 7 107,590,150 (GRCm39) missense probably benign 0.02
IGL01141:Or5p56 APN 7 107,589,758 (GRCm39) missense probably damaging 1.00
R0625:Or5p56 UTSW 7 107,590,396 (GRCm39) missense probably damaging 1.00
R0791:Or5p56 UTSW 7 107,589,740 (GRCm39) missense probably benign 0.27
R1254:Or5p56 UTSW 7 107,589,647 (GRCm39) missense probably benign 0.01
R1456:Or5p56 UTSW 7 107,589,605 (GRCm39) missense probably benign 0.06
R1522:Or5p56 UTSW 7 107,589,740 (GRCm39) missense probably benign 0.27
R1541:Or5p56 UTSW 7 107,590,048 (GRCm39) missense probably benign 0.10
R2889:Or5p56 UTSW 7 107,589,784 (GRCm39) missense probably benign 0.06
R5653:Or5p56 UTSW 7 107,589,592 (GRCm39) missense probably benign 0.38
R6146:Or5p56 UTSW 7 107,589,620 (GRCm39) missense probably damaging 1.00
R6190:Or5p56 UTSW 7 107,590,307 (GRCm39) missense probably damaging 1.00
R7103:Or5p56 UTSW 7 107,589,805 (GRCm39) missense possibly damaging 0.92
R7191:Or5p56 UTSW 7 107,589,853 (GRCm39) missense possibly damaging 0.88
R7553:Or5p56 UTSW 7 107,589,682 (GRCm39) missense probably benign 0.03
R7681:Or5p56 UTSW 7 107,590,355 (GRCm39) missense possibly damaging 0.80
Z1088:Or5p56 UTSW 7 107,589,938 (GRCm39) missense probably benign 0.42
Z1177:Or5p56 UTSW 7 107,590,301 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16