Incidental Mutation 'IGL03071:Or10j5'
ID 417500
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or10j5
Ensembl Gene ENSMUSG00000037924
Gene Name olfactory receptor family 10 subfamily J member 5
Synonyms Olfr16, MOR267-13, GA_x6K02T2R7CC-893157-892228, MOR23
Accession Numbers
Essential gene? Probably non essential (E-score: 0.128) question?
Stock # IGL03071
Quality Score
Status
Chromosome 1
Chromosomal Location 172784335-172785384 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 172784502 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 47 (T47A)
Ref Sequence ENSEMBL: ENSMUSP00000149249 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000038432] [ENSMUST00000215254]
AlphaFold Q62007
Predicted Effect probably benign
Transcript: ENSMUST00000038432
AA Change: T47A

PolyPhen 2 Score 0.014 (Sensitivity: 0.96; Specificity: 0.79)
SMART Domains Protein: ENSMUSP00000041524
Gene: ENSMUSG00000037924
AA Change: T47A

DomainStartEndE-ValueType
Pfam:7tm_4 31 307 7.5e-51 PFAM
Pfam:7tm_1 41 289 3.4e-22 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000215254
AA Change: T47A

PolyPhen 2 Score 0.014 (Sensitivity: 0.96; Specificity: 0.79)
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: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam39 T A 8: 41,278,104 (GRCm39) L165H probably benign Het
Ahnak T C 19: 8,989,282 (GRCm39) I3522T possibly damaging Het
Anks1 G A 17: 28,227,173 (GRCm39) A609T probably benign Het
Apaf1 T C 10: 90,833,117 (GRCm39) D1138G possibly damaging Het
Appl2 T C 10: 83,476,970 (GRCm39) probably null Het
Arhgef19 A T 4: 140,976,313 (GRCm39) I385F possibly damaging Het
Cby3 A G 11: 50,250,343 (GRCm39) D183G probably damaging Het
Ccdc134 G A 15: 82,018,826 (GRCm39) V119M possibly damaging Het
Ccdc180 G T 4: 45,903,840 (GRCm39) probably benign Het
Clec2d T C 6: 129,160,165 (GRCm39) S60P probably benign Het
Cts6 A T 13: 61,350,064 (GRCm39) F6I probably damaging Het
Cyyr1 G A 16: 85,262,449 (GRCm39) H103Y probably damaging Het
Dop1a T A 9: 86,371,668 (GRCm39) S120T possibly damaging Het
Dot1l T C 10: 80,624,513 (GRCm39) S994P probably benign Het
Eya4 T G 10: 23,198,971 (GRCm39) D3A probably benign Het
Fhip2b A G 14: 70,823,649 (GRCm39) C574R probably damaging Het
Fut2 C T 7: 45,300,193 (GRCm39) G193E possibly damaging Het
Gria1 A T 11: 56,902,936 (GRCm39) probably null Het
Hectd1 T C 12: 51,815,957 (GRCm39) T1377A probably benign Het
Magi3 T G 3: 103,923,202 (GRCm39) K1172Q possibly damaging Het
Map3k1 A C 13: 111,892,059 (GRCm39) D1065E possibly damaging Het
Mindy4b-ps A T 3: 58,717,158 (GRCm39) V242D probably damaging Het
Mrgpra3 T C 7: 47,238,929 (GRCm39) probably benign Het
Mroh9 C A 1: 162,866,766 (GRCm39) G657C probably damaging Het
Ogfod1 T C 8: 94,784,395 (GRCm39) W318R probably damaging Het
Pacsin3 G A 2: 91,090,837 (GRCm39) R48H probably damaging Het
Plcb1 A G 2: 135,229,722 (GRCm39) E1114G probably damaging Het
Prkdc T G 16: 15,617,848 (GRCm39) D3226E probably benign Het
Prl4a1 A T 13: 28,204,246 (GRCm39) E96V probably benign Het
Robo4 T C 9: 37,315,580 (GRCm39) probably benign Het
Scn7a G A 2: 66,530,291 (GRCm39) L685F possibly damaging Het
Spata1 A G 3: 146,181,089 (GRCm39) Y290H possibly damaging Het
Tex10 T C 4: 48,452,946 (GRCm39) D671G probably benign Het
Tifa T G 3: 127,590,728 (GRCm39) Y166* probably null Het
Tnfsf10 G A 3: 27,389,769 (GRCm39) D277N probably damaging Het
Tram1 A T 1: 13,649,998 (GRCm39) Y75* probably null Het
Vmn1r60 T A 7: 5,547,368 (GRCm39) N244I probably damaging Het
Xpo4 A G 14: 57,855,685 (GRCm39) I248T possibly damaging Het
Zc2hc1a A G 3: 7,589,182 (GRCm39) probably benign Het
Zfp386 T A 12: 116,022,760 (GRCm39) H124Q probably benign Het
Other mutations in Or10j5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00334:Or10j5 APN 1 172,785,158 (GRCm39) missense possibly damaging 0.66
IGL00336:Or10j5 APN 1 172,785,045 (GRCm39) missense probably benign 0.30
IGL01155:Or10j5 APN 1 172,784,491 (GRCm39) missense probably benign 0.43
IGL01549:Or10j5 APN 1 172,784,541 (GRCm39) missense probably damaging 1.00
IGL02679:Or10j5 APN 1 172,784,743 (GRCm39) missense probably damaging 1.00
IGL03352:Or10j5 APN 1 172,784,850 (GRCm39) missense probably benign 0.00
R0449:Or10j5 UTSW 1 172,784,965 (GRCm39) missense probably damaging 1.00
R1725:Or10j5 UTSW 1 172,784,908 (GRCm39) missense possibly damaging 0.90
R1726:Or10j5 UTSW 1 172,784,658 (GRCm39) missense probably benign 0.00
R1735:Or10j5 UTSW 1 172,784,374 (GRCm39) missense probably benign
R1928:Or10j5 UTSW 1 172,784,881 (GRCm39) missense probably damaging 0.98
R4258:Or10j5 UTSW 1 172,785,205 (GRCm39) missense possibly damaging 0.88
R4359:Or10j5 UTSW 1 172,784,647 (GRCm39) missense probably benign
R4434:Or10j5 UTSW 1 172,785,111 (GRCm39) missense probably damaging 1.00
R4666:Or10j5 UTSW 1 172,785,157 (GRCm39) missense probably benign
R4874:Or10j5 UTSW 1 172,785,166 (GRCm39) missense probably benign 0.00
R5063:Or10j5 UTSW 1 172,785,009 (GRCm39) missense possibly damaging 0.48
R5988:Or10j5 UTSW 1 172,784,723 (GRCm39) nonsense probably null
R6074:Or10j5 UTSW 1 172,784,945 (GRCm39) missense probably benign 0.10
R7021:Or10j5 UTSW 1 172,784,494 (GRCm39) missense probably benign 0.01
R7234:Or10j5 UTSW 1 172,784,673 (GRCm39) missense probably damaging 0.96
R7527:Or10j5 UTSW 1 172,784,511 (GRCm39) missense probably benign 0.00
R8271:Or10j5 UTSW 1 172,784,744 (GRCm39) nonsense probably null
R8890:Or10j5 UTSW 1 172,785,045 (GRCm39) missense probably benign 0.30
R8906:Or10j5 UTSW 1 172,784,186 (GRCm39) start gained probably benign
R9048:Or10j5 UTSW 1 172,784,929 (GRCm39) missense probably benign
R9583:Or10j5 UTSW 1 172,784,893 (GRCm39) missense probably damaging 1.00
Z1088:Or10j5 UTSW 1 172,784,891 (GRCm39) missense probably damaging 1.00
Posted On 2016-08-02