Mutagenetix > Incidental Mutation

Incidental Mutation 'R0026:Mrgprx2'

189171

Institutional Source

Beutler Lab

Gene Symbol

Mrgprx2

Ensembl Gene

ENSMUSG00000074109

Gene Name

MAS-related GPR, member X2

Synonyms

MrgB10, Mrgprb10

MMRRC Submission

038321-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.058) question?

Stock #

R0026 (G1)

Quality Score

Status

Validated

Chromosome

Chromosomal Location

48478619-48499321 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 48482023 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Histidine to Leucine at position 106 (H106L)

Ref Sequence

ENSEMBL: ENSMUSP00000140945 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000098433] [ENSMUST00000186394]

AlphaFold

Q3UG50

Predicted Effect

probably benign
Transcript: ENSMUST00000098433
AA Change: H349L

PolyPhen 2 Score 0.057 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000127022
Gene: ENSMUSG00000074109
AA Change: H349L

Domain	Start	End	E-Value	Type
Pfam:7TM_GPCR_Srx	50	230	4.6e-10	PFAM
Pfam:7tm_1	59	290	1e-6	PFAM
low complexity region	319	334	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000186394
AA Change: H106L

PolyPhen 2 Score 0.663 (Sensitivity: 0.86; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000140945
Gene: ENSMUSG00000074109
AA Change: H106L

Domain	Start	End	E-Value	Type
SCOP:d1l9ha_	11	50	1e-5	SMART
low complexity region	76	91	N/A	INTRINSIC

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 99.3%
3x: 98.9%
10x: 97.8%
20x: 96.3%

Validation Efficiency

93% (70/75)

Allele List at MGI

Other mutations in this stock

Total: 61 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1110002E22Rik	T	A	3: 138,066,805 (GRCm38)	I585N	possibly damaging	Het
4931408C20Rik	T	A	1: 26,683,369 (GRCm38)	D910V	probably benign	Het
A830005F24Rik	C	T	13: 48,514,372 (GRCm38)		probably benign	Het
Abca16	C	T	7: 120,477,923 (GRCm38)		probably benign	Het
Acot10	G	A	15: 20,666,236 (GRCm38)	L140F	probably benign	Het
Adam19	G	T	11: 46,136,259 (GRCm38)	C573F	probably damaging	Het
Aff3	A	G	1: 38,203,893 (GRCm38)	S948P	probably benign	Het
Anxa3	T	A	5: 96,838,401 (GRCm38)	Y300N	probably benign	Het
BC016579	T	C	16: 45,640,367 (GRCm38)	T113A	probably benign	Het
Bmpr1b	A	G	3: 141,870,733 (GRCm38)	L113P	probably benign	Het
Casq1	T	C	1: 172,219,400 (GRCm38)		probably benign	Het
Cdc16	T	A	8: 13,759,130 (GRCm38)		probably null	Het
Cep135	C	T	5: 76,606,734 (GRCm38)	R353*	probably null	Het
Cma1	A	T	14: 55,942,164 (GRCm38)	C188S	probably damaging	Het
Csf3r	A	G	4: 126,031,884 (GRCm38)	T151A	probably benign	Het
Cyp4b1	C	T	4: 115,647,521 (GRCm38)	G56D	possibly damaging	Het
Dbn1	T	C	13: 55,477,784 (GRCm38)	E275G	probably damaging	Het
Dlgap2	C	T	8: 14,727,363 (GRCm38)	Q203*	probably null	Het
Ephb3	A	G	16: 21,214,917 (GRCm38)	D251G	probably damaging	Het
Fancd2os	G	T	6: 113,597,691 (GRCm38)	T118N	probably damaging	Het
Gm10801	T	C	2: 98,663,909 (GRCm38)		probably benign	Het
Got1l1	C	T	8: 27,200,248 (GRCm38)	V132I	probably benign	Het
H2-M9	T	C	17: 36,641,527 (GRCm38)		probably benign	Het
Ibtk	A	G	9: 85,690,303 (GRCm38)	V1278A	probably benign	Het
Kctd3	T	C	1: 188,976,621 (GRCm38)	T519A	probably damaging	Het
Lgsn	T	A	1: 31,203,443 (GRCm38)	V202D	probably damaging	Het
Madd	A	G	2: 91,175,708 (GRCm38)	F381L	possibly damaging	Het
Map1s	G	A	8: 70,914,638 (GRCm38)	G729D	probably damaging	Het
Mlycd	A	G	8: 119,410,435 (GRCm38)	I465V	probably benign	Het
Mrgprb1	T	C	7: 48,447,204 (GRCm38)	R108G	possibly damaging	Het
Ncor1	T	C	11: 62,438,429 (GRCm38)	Y6C	probably damaging	Het
Nfkb1	T	C	3: 135,591,573 (GRCm38)	D773G	probably damaging	Het
Nxnl1	A	G	8: 71,566,573 (GRCm38)	S3P	probably damaging	Het
Olfr109	T	A	17: 37,466,803 (GRCm38)	V199D	probably damaging	Het
Olfr921	G	A	9: 38,775,596 (GRCm38)	V114I	probably benign	Het
Otud7a	T	C	7: 63,735,801 (GRCm38)	F338L	probably benign	Het
Pdcl3	T	A	1: 38,991,280 (GRCm38)	L14Q	probably damaging	Het
Pla2g7	T	A	17: 43,594,930 (GRCm38)		probably benign	Het
Prpf31	T	A	7: 3,639,668 (GRCm38)	N413K	probably benign	Het
Rapgef5	T	C	12: 117,689,161 (GRCm38)	S307P	probably benign	Het
Relt	C	A	7: 100,850,221 (GRCm38)	E164*	probably null	Het
Rnf185	T	C	11: 3,426,617 (GRCm38)	D86G	probably damaging	Het
Rrm2b	T	C	15: 37,953,741 (GRCm38)	E21G	probably benign	Het
Scn5a	A	G	9: 119,522,566 (GRCm38)	I783T	probably damaging	Het
Senp1	T	C	15: 98,076,668 (GRCm38)	R88G	probably damaging	Het
Skint5	A	T	4: 113,546,468 (GRCm38)		probably benign	Het
Slc35b1	T	C	11: 95,390,642 (GRCm38)	S294P	probably benign	Het
Slc5a2	T	A	7: 128,270,053 (GRCm38)	I335N	probably damaging	Het
Sstr1	T	A	12: 58,212,858 (GRCm38)	M89K	probably damaging	Het
Szt2	A	T	4: 118,384,772 (GRCm38)	S1612R	possibly damaging	Het
Taf1c	T	C	8: 119,604,236 (GRCm38)		probably null	Het
Taf1d	T	A	9: 15,308,648 (GRCm38)	S64R	probably damaging	Het
Tmem125	A	G	4: 118,542,073 (GRCm38)	S54P	possibly damaging	Het
Ttf1	T	A	2: 29,071,349 (GRCm38)	I583N	possibly damaging	Het
Uchl4	A	T	9: 64,235,371 (GRCm38)		probably null	Het
Unc5b	A	T	10: 60,774,592 (GRCm38)	I482N	possibly damaging	Het
Unc80	C	A	1: 66,521,584 (GRCm38)	Q824K	probably benign	Het
Utrn	T	C	10: 12,726,196 (GRCm38)		probably benign	Het
Vmn2r61	T	G	7: 42,275,474 (GRCm38)	I484R	possibly damaging	Het
Vps13b	T	C	15: 35,923,301 (GRCm38)	I3774T	possibly damaging	Het
Yipf1	T	A	4: 107,345,160 (GRCm38)	L240*	probably null	Het

Other mutations in Mrgprx2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01603:Mrgprx2	APN	7	48,482,626 (GRCm38)	missense	probably damaging	1.00
IGL01655:Mrgprx2	APN	7	48,482,691 (GRCm38)	nonsense	probably null
IGL02052:Mrgprx2	APN	7	48,482,294 (GRCm38)	missense	possibly damaging	0.75
IGL02254:Mrgprx2	APN	7	48,482,938 (GRCm38)	missense	probably benign	0.16
IGL02985:Mrgprx2	APN	7	48,482,497 (GRCm38)	missense	probably damaging	0.98
R0387:Mrgprx2	UTSW	7	48,499,160 (GRCm38)	start codon destroyed	probably null	0.98
R0514:Mrgprx2	UTSW	7	48,482,964 (GRCm38)	start codon destroyed	probably null
R0650:Mrgprx2	UTSW	7	48,482,918 (GRCm38)	missense	probably damaging	0.96
R1014:Mrgprx2	UTSW	7	48,482,558 (GRCm38)	splice site	probably null
R2011:Mrgprx2	UTSW	7	48,482,534 (GRCm38)	missense	probably damaging	0.96
R2224:Mrgprx2	UTSW	7	48,482,860 (GRCm38)	missense	probably benign	0.43
R4238:Mrgprx2	UTSW	7	48,482,990 (GRCm38)	missense	probably benign
R4846:Mrgprx2	UTSW	7	48,482,836 (GRCm38)	missense	probably damaging	1.00
R5385:Mrgprx2	UTSW	7	48,483,005 (GRCm38)	missense	probably benign	0.11
R5891:Mrgprx2	UTSW	7	48,482,246 (GRCm38)	missense	probably benign
R6490:Mrgprx2	UTSW	7	48,482,869 (GRCm38)	missense	probably damaging	1.00
R6576:Mrgprx2	UTSW	7	48,482,632 (GRCm38)	missense	probably damaging	1.00
R6934:Mrgprx2	UTSW	7	48,482,065 (GRCm38)	missense	possibly damaging	0.79
R6948:Mrgprx2	UTSW	7	48,482,716 (GRCm38)	missense	possibly damaging	0.52
R7938:Mrgprx2	UTSW	7	48,482,492 (GRCm38)	missense	probably benign	0.01
R7944:Mrgprx2	UTSW	7	48,483,005 (GRCm38)	missense	probably benign	0.11
R7945:Mrgprx2	UTSW	7	48,483,005 (GRCm38)	missense	probably benign	0.11
R8221:Mrgprx2	UTSW	7	48,482,779 (GRCm38)	missense	probably benign	0.00
R8750:Mrgprx2	UTSW	7	48,482,030 (GRCm38)	missense	probably benign
R8782:Mrgprx2	UTSW	7	48,482,551 (GRCm38)	missense	probably damaging	0.98
R9015:Mrgprx2	UTSW	7	48,499,190 (GRCm38)	unclassified	probably benign
X0027:Mrgprx2	UTSW	7	48,482,498 (GRCm38)	missense	probably damaging	1.00
X0063:Mrgprx2	UTSW	7	48,482,798 (GRCm38)	missense	probably benign	0.04
Z1176:Mrgprx2	UTSW	7	48,482,342 (GRCm38)	missense	probably damaging	0.98

Predicted Primers

PCR Primer
(F):5'- AGTTGGTAAAACCCTGAGCAAGATAGC -3'
(R):5'- CTTACACAAGATTCCTGTGACCAGGC -3'

Sequencing Primer
(F):5'- CCAACTGAGTTAACCTTGGGTCA -3'
(R):5'- CCTTGTAGTATATATCCGGTCACAG -3'

Posted On

2014-05-13