Incidental Mutation 'IGL03071:Mrgpra3'
ID 417535
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Mrgpra3
Ensembl Gene ENSMUSG00000078698
Gene Name MAS-related GPR, member A3
Synonyms G protein-coupled receptor, MrgA3
Accession Numbers
Essential gene? Probably non essential (E-score: 0.048) question?
Stock # IGL03071
Quality Score
Status
Chromosome 7
Chromosomal Location 47238698-47251120 bp(-) (GRCm39)
Type of Mutation utr 3 prime
DNA Base Change (assembly) T to C at 47238929 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000135437 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000176369]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000176369
SMART Domains Protein: ENSMUSP00000135437
Gene: ENSMUSG00000078698

DomainStartEndE-ValueType
low complexity region 14 31 N/A INTRINSIC
Pfam:7TM_GPCR_Srx 48 234 6.3e-7 PFAM
Pfam:7tm_1 57 286 2.7e-9 PFAM
Coding Region Coverage
Validation Efficiency
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
Mroh9 C A 1: 162,866,766 (GRCm39) G657C probably damaging Het
Ogfod1 T C 8: 94,784,395 (GRCm39) W318R probably damaging Het
Or10j5 A G 1: 172,784,502 (GRCm39) T47A probably benign 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 Mrgpra3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00162:Mrgpra3 APN 7 47,239,267 (GRCm39) missense probably benign 0.00
IGL02097:Mrgpra3 APN 7 47,239,204 (GRCm39) missense possibly damaging 0.94
IGL02101:Mrgpra3 APN 7 47,239,300 (GRCm39) missense probably damaging 0.99
PIT4445001:Mrgpra3 UTSW 7 47,239,908 (GRCm39) missense possibly damaging 0.88
R0828:Mrgpra3 UTSW 7 47,239,884 (GRCm39) missense probably benign 0.12
R1118:Mrgpra3 UTSW 7 47,239,039 (GRCm39) missense possibly damaging 0.83
R1835:Mrgpra3 UTSW 7 47,239,694 (GRCm39) nonsense probably null
R2258:Mrgpra3 UTSW 7 47,239,842 (GRCm39) missense probably benign 0.35
R2393:Mrgpra3 UTSW 7 47,239,365 (GRCm39) missense possibly damaging 0.92
R3437:Mrgpra3 UTSW 7 47,239,314 (GRCm39) missense probably damaging 1.00
R3973:Mrgpra3 UTSW 7 47,239,414 (GRCm39) missense probably benign 0.22
R4273:Mrgpra3 UTSW 7 47,239,180 (GRCm39) missense probably benign 0.01
R4495:Mrgpra3 UTSW 7 47,239,813 (GRCm39) missense probably benign 0.00
R4768:Mrgpra3 UTSW 7 47,239,476 (GRCm39) missense possibly damaging 0.94
R4822:Mrgpra3 UTSW 7 47,239,716 (GRCm39) missense possibly damaging 0.69
R4967:Mrgpra3 UTSW 7 47,239,267 (GRCm39) missense probably benign 0.33
R5207:Mrgpra3 UTSW 7 47,239,909 (GRCm39) missense probably benign 0.06
R5569:Mrgpra3 UTSW 7 47,239,759 (GRCm39) missense probably benign 0.00
R5763:Mrgpra3 UTSW 7 47,239,355 (GRCm39) nonsense probably null
R6102:Mrgpra3 UTSW 7 47,239,897 (GRCm39) missense possibly damaging 0.92
R6612:Mrgpra3 UTSW 7 47,239,783 (GRCm39) missense probably benign 0.00
R6718:Mrgpra3 UTSW 7 47,239,444 (GRCm39) missense probably benign 0.25
R6859:Mrgpra3 UTSW 7 47,239,781 (GRCm39) missense probably benign 0.04
R7029:Mrgpra3 UTSW 7 47,239,290 (GRCm39) missense probably benign 0.00
R7034:Mrgpra3 UTSW 7 47,239,838 (GRCm39) missense possibly damaging 0.49
R7036:Mrgpra3 UTSW 7 47,239,838 (GRCm39) missense possibly damaging 0.49
R7097:Mrgpra3 UTSW 7 47,239,389 (GRCm39) missense probably benign
R7475:Mrgpra3 UTSW 7 47,239,695 (GRCm39) missense probably damaging 1.00
R8289:Mrgpra3 UTSW 7 47,239,468 (GRCm39) missense possibly damaging 0.76
R8315:Mrgpra3 UTSW 7 47,251,051 (GRCm39) start codon destroyed probably null 0.93
R9500:Mrgpra3 UTSW 7 47,239,400 (GRCm39) nonsense probably null
Z1177:Mrgpra3 UTSW 7 47,251,049 (GRCm39) nonsense probably null
Posted On 2016-08-02