Incidental Mutation 'IGL01317:Mrgpra1'
ID 73887
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Mrgpra1
Ensembl Gene ENSMUSG00000050650
Gene Name MAS-related GPR, member A1
Synonyms MrgA1
Accession Numbers
Essential gene? Probably non essential (E-score: 0.070) question?
Stock # IGL01317
Quality Score
Status
Chromosome 7
Chromosomal Location 46984623-47003988 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 46985372 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Lysine at position 102 (N102K)
Ref Sequence ENSEMBL: ENSMUSP00000129978 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000098438]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000098438
AA Change: N102K

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000129978
Gene: ENSMUSG00000050650
AA Change: N102K

DomainStartEndE-ValueType
low complexity region 14 27 N/A INTRINSIC
low complexity region 36 49 N/A INTRINSIC
Pfam:7tm_1 57 225 2.1e-8 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam32 A T 8: 25,362,597 (GRCm39) D609E probably damaging Het
Aldh3b1 T C 19: 3,968,104 (GRCm39) I352V probably benign Het
Apeh A T 9: 107,963,406 (GRCm39) S605R probably benign Het
Arhgap32 A G 9: 32,168,260 (GRCm39) K748E probably benign Het
Avpr1a T C 10: 122,285,472 (GRCm39) S255P probably benign Het
Cadps2 T A 6: 23,314,172 (GRCm39) D1124V possibly damaging Het
Cask C T X: 13,388,499 (GRCm39) E83K probably damaging Het
Cep170b A G 12: 112,704,078 (GRCm39) Y670C probably damaging Het
Chd3 A G 11: 69,244,037 (GRCm39) Y1343H probably damaging Het
Cit T A 5: 116,046,775 (GRCm39) V396D probably benign Het
Cldn18 T C 9: 99,578,135 (GRCm39) T203A probably benign Het
Dido1 A C 2: 180,313,550 (GRCm39) N907K probably benign Het
Dmbt1 T A 7: 130,642,921 (GRCm39) D246E probably damaging Het
Dph1 T C 11: 75,071,486 (GRCm39) H303R probably benign Het
Dspp T A 5: 104,321,914 (GRCm39) Y8N probably damaging Het
Efhc2 C T X: 17,071,198 (GRCm39) probably benign Het
Fam171a1 T A 2: 3,203,663 (GRCm39) V215E probably damaging Het
Fhip1a T C 3: 85,580,153 (GRCm39) D684G probably benign Het
Foxm1 T A 6: 128,344,316 (GRCm39) M22K probably damaging Het
Gdpd4 A C 7: 97,647,465 (GRCm39) M371L possibly damaging Het
Hdac9 T C 12: 34,479,488 (GRCm39) probably benign Het
Heatr1 T A 13: 12,413,908 (GRCm39) W162R probably damaging Het
Hydin A T 8: 111,053,078 (GRCm39) D250V probably damaging Het
Itga4 T A 2: 79,153,005 (GRCm39) C897* probably null Het
Itprid1 G T 6: 55,944,790 (GRCm39) A504S possibly damaging Het
Kcnd2 T C 6: 21,727,339 (GRCm39) *631Q probably null Het
Kcnn2 A G 18: 45,693,694 (GRCm39) probably null Het
Lama1 A T 17: 68,125,696 (GRCm39) E2951V probably damaging Het
Lyst A G 13: 13,845,455 (GRCm39) Q1944R probably benign Het
Mmp14 A G 14: 54,673,247 (GRCm39) T52A possibly damaging Het
Mrpl28 G A 17: 26,344,489 (GRCm39) G205D probably damaging Het
Mtmr4 T C 11: 87,493,230 (GRCm39) probably benign Het
Oog2 A G 4: 143,921,837 (GRCm39) N249S probably benign Het
Or4f57 T A 2: 111,790,620 (GRCm39) H266L possibly damaging Het
Ppp6r2 T A 15: 89,170,131 (GRCm39) V882E possibly damaging Het
Qser1 A C 2: 104,617,324 (GRCm39) Y1073D probably damaging Het
Rbl2 C A 8: 91,826,685 (GRCm39) D480E probably damaging Het
Rfx7 G A 9: 72,525,818 (GRCm39) G1003S probably damaging Het
Rrh A C 3: 129,616,074 (GRCm39) F20V possibly damaging Het
Rwdd3 A G 3: 120,965,282 (GRCm39) I15T possibly damaging Het
Sestd1 A T 2: 77,022,889 (GRCm39) M493K possibly damaging Het
Slc17a8 T A 10: 89,456,666 (GRCm39) L32F probably benign Het
Slc29a4 A G 5: 142,691,285 (GRCm39) D55G probably benign Het
Tbc1d10a A T 11: 4,162,826 (GRCm39) Y223F probably benign Het
Tbx20 A G 9: 24,681,051 (GRCm39) V147A probably damaging Het
Tmem63c A T 12: 87,118,770 (GRCm39) probably benign Het
Tmtc2 C A 10: 105,249,646 (GRCm39) R29L probably damaging Het
Ttc21b T A 2: 66,018,700 (GRCm39) M1236L probably benign Het
Unc119 T A 11: 78,238,052 (GRCm39) C12S probably damaging Het
Vcan A G 13: 89,839,787 (GRCm39) M1919T probably benign Het
Zmat4 C A 8: 24,392,185 (GRCm39) T47K probably benign Het
Other mutations in Mrgpra1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00903:Mrgpra1 APN 7 46,985,326 (GRCm39) missense probably benign 0.00
IGL01718:Mrgpra1 APN 7 46,985,675 (GRCm39) splice site probably null
IGL02252:Mrgpra1 APN 7 46,984,912 (GRCm39) missense probably benign 0.00
IGL03301:Mrgpra1 APN 7 46,985,164 (GRCm39) missense probably benign
R0012:Mrgpra1 UTSW 7 46,985,218 (GRCm39) missense probably damaging 0.98
R1019:Mrgpra1 UTSW 7 46,984,833 (GRCm39) missense probably benign 0.00
R2224:Mrgpra1 UTSW 7 46,984,854 (GRCm39) missense possibly damaging 0.50
R2520:Mrgpra1 UTSW 7 46,985,020 (GRCm39) missense possibly damaging 0.75
R2924:Mrgpra1 UTSW 7 46,984,618 (GRCm39) splice site probably null
R3038:Mrgpra1 UTSW 7 46,984,744 (GRCm39) nonsense probably null
R3900:Mrgpra1 UTSW 7 46,985,275 (GRCm39) missense possibly damaging 0.76
R4692:Mrgpra1 UTSW 7 46,985,446 (GRCm39) missense probably damaging 1.00
R4783:Mrgpra1 UTSW 7 46,985,218 (GRCm39) missense probably damaging 0.98
R4784:Mrgpra1 UTSW 7 46,985,218 (GRCm39) missense probably damaging 0.98
R4785:Mrgpra1 UTSW 7 46,985,218 (GRCm39) missense probably damaging 0.98
R4981:Mrgpra1 UTSW 7 46,984,959 (GRCm39) missense probably damaging 1.00
R5031:Mrgpra1 UTSW 7 46,984,985 (GRCm39) nonsense probably null
R6760:Mrgpra1 UTSW 7 46,984,789 (GRCm39) missense probably benign 0.03
R7305:Mrgpra1 UTSW 7 46,985,203 (GRCm39) missense probably benign 0.38
R7348:Mrgpra1 UTSW 7 46,985,157 (GRCm39) missense probably benign 0.09
R7837:Mrgpra1 UTSW 7 46,985,076 (GRCm39) missense possibly damaging 0.68
R8158:Mrgpra1 UTSW 7 46,985,204 (GRCm39) nonsense probably null
R8856:Mrgpra1 UTSW 7 46,985,583 (GRCm39) missense probably benign 0.30
R9100:Mrgpra1 UTSW 7 46,984,732 (GRCm39) missense probably damaging 0.97
R9694:Mrgpra1 UTSW 7 46,985,268 (GRCm39) missense probably damaging 1.00
X0012:Mrgpra1 UTSW 7 46,985,623 (GRCm39) missense probably benign
Posted On 2013-10-07