Incidental Mutation 'IGL01629:Mrgprx3-ps'
ID 92856
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Mrgprx3-ps
Ensembl Gene ENSMUSG00000099560
Gene Name MAS-related GPR, member X3, pseudogene
Synonyms LOC269919, Gm660, Gm19419
Accession Numbers
Essential gene? Probably non essential (E-score: 0.238) question?
Stock # IGL01629
Quality Score
Status
Chromosome 7
Chromosomal Location 46959126-46960043 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 46959353 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Stop codon at position 213 (K213*)
Ref Sequence ENSEMBL: ENSMUSP00000136396 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000179005]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000179005
AA Change: K213*
SMART Domains Protein: ENSMUSP00000136396
Gene: ENSMUSG00000074111
AA Change: K213*

DomainStartEndE-ValueType
Pfam:7tm_1 12 178 3.4e-9 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000187741
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgra2 G A 8: 27,608,761 (GRCm39) A540T possibly damaging Het
Adm2 T A 15: 89,207,605 (GRCm39) probably null Het
Alox12 G A 11: 70,133,660 (GRCm39) P555S probably damaging Het
Alpk2 A G 18: 65,433,113 (GRCm39) S1798P probably damaging Het
Amfr T A 8: 94,714,136 (GRCm39) probably null Het
Arhgef18 T A 8: 3,431,942 (GRCm39) C168S possibly damaging Het
Atxn7l3 A T 11: 102,183,320 (GRCm39) probably benign Het
Ccdc191 A G 16: 43,779,663 (GRCm39) K707E possibly damaging Het
Cdc5l G T 17: 45,724,116 (GRCm39) D391E probably benign Het
Cmtm2b T C 8: 105,056,420 (GRCm39) S110P possibly damaging Het
Cyp2j8 T C 4: 96,387,840 (GRCm39) D207G probably damaging Het
Ddhd2 A G 8: 26,225,855 (GRCm39) F501L possibly damaging Het
Dnaaf6rt T A 1: 31,262,014 (GRCm39) probably null Het
Dnah1 C T 14: 31,014,277 (GRCm39) V1823M probably damaging Het
Gjb4 T C 4: 127,245,419 (GRCm39) D174G possibly damaging Het
Gm45213 A G 7: 65,711,962 (GRCm39) D58G probably damaging Het
Hes1 C T 16: 29,884,976 (GRCm39) probably benign Het
Krt33b T A 11: 99,920,386 (GRCm39) Q89L probably benign Het
Llcfc1 C A 6: 41,661,459 (GRCm39) S3Y possibly damaging Het
Ltf A G 9: 110,864,874 (GRCm39) N569S probably damaging Het
Mknk1 T A 4: 115,732,731 (GRCm39) W320R probably damaging Het
Mslnl T G 17: 25,963,749 (GRCm39) V388G possibly damaging Het
Nfkb1 T C 3: 135,307,228 (GRCm39) I566V probably benign Het
Npy1r G A 8: 67,156,873 (GRCm39) V98I probably benign Het
Phf1 G T 17: 27,153,247 (GRCm39) A22S probably benign Het
Plcg1 T G 2: 160,599,930 (GRCm39) F897V possibly damaging Het
Ric1 A T 19: 29,581,381 (GRCm39) E1367D probably benign Het
Slc24a3 T C 2: 145,482,130 (GRCm39) probably benign Het
Sorl1 A G 9: 41,968,565 (GRCm39) probably null Het
Speer4a2 C T 5: 26,290,700 (GRCm39) S157N probably damaging Het
Spink5 T C 18: 44,129,677 (GRCm39) probably benign Het
Syne2 A G 12: 76,051,377 (GRCm39) I4036V possibly damaging Het
Taok1 A T 11: 77,429,030 (GRCm39) M890K possibly damaging Het
Tenm2 A T 11: 36,755,711 (GRCm39) Y96N probably damaging Het
Ttll10 T A 4: 156,131,351 (GRCm39) T233S probably benign Het
Vps39 G T 2: 120,154,079 (GRCm39) L628M probably benign Het
Zfp563 G A 17: 33,323,600 (GRCm39) R105H probably damaging Het
Other mutations in Mrgprx3-ps
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01919:Mrgprx3-ps APN 7 46,959,959 (GRCm39) missense probably benign 0.00
IGL02455:Mrgprx3-ps APN 7 46,959,263 (GRCm39) exon noncoding transcript
R0218:Mrgprx3-ps UTSW 7 46,959,154 (GRCm39) missense possibly damaging 0.87
R0308:Mrgprx3-ps UTSW 7 46,959,766 (GRCm39) missense probably benign 0.25
R4003:Mrgprx3-ps UTSW 7 46,959,959 (GRCm39) missense probably benign 0.00
R4274:Mrgprx3-ps UTSW 7 46,959,574 (GRCm39) exon noncoding transcript
R4411:Mrgprx3-ps UTSW 7 46,959,746 (GRCm39) exon noncoding transcript
R4413:Mrgprx3-ps UTSW 7 46,959,746 (GRCm39) exon noncoding transcript
R5254:Mrgprx3-ps UTSW 7 46,959,184 (GRCm39) exon noncoding transcript
Posted On 2013-12-09