Incidental Mutation 'IGL02117:Mrgprx1'
ID 280442
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Mrgprx1
Ensembl Gene ENSMUSG00000070552
Gene Name MAS-related GPR, member X1
Synonyms Mrgprc11, MrgC11
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02117
Quality Score
Status
Chromosome 7
Chromosomal Location 47670719-47677345 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to T at 47671371 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Stop codon at position 125 (C125*)
Ref Sequence ENSEMBL: ENSMUSP00000091954 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094390]
AlphaFold Q8CIP3
Predicted Effect probably null
Transcript: ENSMUST00000094390
AA Change: C125*
SMART Domains Protein: ENSMUSP00000091954
Gene: ENSMUSG00000070552
AA Change: C125*

DomainStartEndE-ValueType
Pfam:7tm_1 43 202 1.9e-7 PFAM
low complexity region 227 245 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921509C19Rik T A 2: 151,315,466 (GRCm39) M71L probably benign Het
Abcb11 A G 2: 69,154,169 (GRCm39) probably benign Het
Ago4 T C 4: 126,410,645 (GRCm39) T249A probably benign Het
Ahr A T 12: 35,562,922 (GRCm39) C92* probably null Het
Arhgap17 G A 7: 122,885,996 (GRCm39) probably benign Het
Arid1a G T 4: 133,420,126 (GRCm39) T992K unknown Het
Camk2a A G 18: 61,111,061 (GRCm39) I83M probably damaging Het
Ccdc154 T C 17: 25,386,792 (GRCm39) probably null Het
Chtf18 T C 17: 25,941,177 (GRCm39) H607R possibly damaging Het
Col25a1 T C 3: 130,313,422 (GRCm39) probably benign Het
Col9a1 C T 1: 24,276,574 (GRCm39) Q530* probably null Het
Cryl1 G T 14: 57,523,904 (GRCm39) D219E probably damaging Het
Cul3 A T 1: 80,300,781 (GRCm39) probably benign Het
Cul9 C A 17: 46,851,301 (GRCm39) R373L probably benign Het
Exo1 A G 1: 175,721,309 (GRCm39) Y316C possibly damaging Het
Fam114a1 G A 5: 65,187,465 (GRCm39) V408M probably benign Het
Hmcn2 A T 2: 31,347,185 (GRCm39) S4792C possibly damaging Het
Hps5 A G 7: 46,432,940 (GRCm39) F260S probably damaging Het
Hrh4 T C 18: 13,155,477 (GRCm39) S339P probably benign Het
Ist1 A T 8: 110,405,584 (GRCm39) L152Q probably damaging Het
Marco A G 1: 120,418,683 (GRCm39) V190A probably benign Het
Mdn1 T C 4: 32,709,364 (GRCm39) V1711A probably benign Het
Mmp9 A G 2: 164,791,644 (GRCm39) Y179C probably damaging Het
Mrgprb5 A G 7: 47,818,742 (GRCm39) probably benign Het
Msh6 A G 17: 88,298,234 (GRCm39) probably benign Het
Myot C A 18: 44,488,177 (GRCm39) R441S probably benign Het
Or11g7 A G 14: 50,691,399 (GRCm39) R297G possibly damaging Het
Paf1 A G 7: 28,098,115 (GRCm39) probably benign Het
Pde11a A G 2: 75,821,606 (GRCm39) L891P probably damaging Het
Prkar2a T A 9: 108,596,460 (GRCm39) I135N probably damaging Het
Rap1gap C T 4: 137,454,355 (GRCm39) T646M probably damaging Het
Rgs7bp T C 13: 105,088,087 (GRCm39) D229G possibly damaging Het
Rhobtb3 C T 13: 76,025,547 (GRCm39) S523N probably damaging Het
Setd7 A T 3: 51,428,826 (GRCm39) Y335N probably damaging Het
Setdb2 C T 14: 59,639,764 (GRCm39) R709Q probably damaging Het
Socs4 T C 14: 47,528,264 (GRCm39) Y400H probably damaging Het
Spag16 A T 1: 69,909,479 (GRCm39) H192L probably damaging Het
Ssh1 A T 5: 114,084,541 (GRCm39) C566* probably null Het
Stap1 T G 5: 86,234,552 (GRCm39) I98S possibly damaging Het
Tgs1 C T 4: 3,585,836 (GRCm39) H238Y probably damaging Het
Tifab T C 13: 56,324,275 (GRCm39) Y56C probably benign Het
Tssk2 A G 16: 17,717,653 (GRCm39) E352G probably benign Het
Vmn2r57 A T 7: 41,049,874 (GRCm39) V625D probably benign Het
Wbp1l T C 19: 46,632,876 (GRCm39) Y75H probably benign Het
Wnt5a T C 14: 28,228,077 (GRCm39) probably benign Het
Other mutations in Mrgprx1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01152:Mrgprx1 APN 7 47,671,234 (GRCm39) missense probably benign 0.00
IGL01326:Mrgprx1 APN 7 47,671,517 (GRCm39) missense probably benign 0.26
IGL02219:Mrgprx1 APN 7 47,671,477 (GRCm39) missense probably benign 0.20
IGL02431:Mrgprx1 APN 7 47,670,875 (GRCm39) missense probably benign 0.00
IGL02441:Mrgprx1 APN 7 47,671,336 (GRCm39) missense probably benign 0.39
IGL02682:Mrgprx1 APN 7 47,671,740 (GRCm39) missense probably damaging 1.00
R0219:Mrgprx1 UTSW 7 47,671,294 (GRCm39) missense probably damaging 1.00
R4366:Mrgprx1 UTSW 7 47,670,941 (GRCm39) missense probably damaging 0.98
R4521:Mrgprx1 UTSW 7 47,671,447 (GRCm39) missense probably benign
R4801:Mrgprx1 UTSW 7 47,670,959 (GRCm39) missense possibly damaging 0.89
R4802:Mrgprx1 UTSW 7 47,670,959 (GRCm39) missense possibly damaging 0.89
R5452:Mrgprx1 UTSW 7 47,671,556 (GRCm39) missense probably benign 0.07
R5537:Mrgprx1 UTSW 7 47,670,898 (GRCm39) missense probably benign
R6444:Mrgprx1 UTSW 7 47,671,562 (GRCm39) missense possibly damaging 0.87
R6834:Mrgprx1 UTSW 7 47,671,385 (GRCm39) missense probably damaging 0.99
R7406:Mrgprx1 UTSW 7 47,671,733 (GRCm39) missense possibly damaging 0.62
R9664:Mrgprx1 UTSW 7 47,671,273 (GRCm39) missense probably benign 0.38
RF020:Mrgprx1 UTSW 7 47,671,259 (GRCm39) small insertion probably benign
RF024:Mrgprx1 UTSW 7 47,671,259 (GRCm39) small insertion probably benign
RF026:Mrgprx1 UTSW 7 47,671,257 (GRCm39) small insertion probably benign
RF043:Mrgprx1 UTSW 7 47,671,257 (GRCm39) small insertion probably benign
Z1088:Mrgprx1 UTSW 7 47,670,877 (GRCm39) missense probably damaging 0.98
Posted On 2015-04-16