Mutagenetix > Incidental Mutation

Incidental Mutation 'R3973:Mrgpra3'

312936

Institutional Source

Beutler Lab

Gene Symbol

Mrgpra3

Ensembl Gene

ENSMUSG00000078698

Gene Name

MAS-related GPR, member A3

Synonyms

G protein-coupled receptor, MrgA3

MMRRC Submission

040841-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.048) question?

Stock #

R3973 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

47238698-47251120 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 47239414 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Phenylalanine at position 171 (I171F)

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
AA Change: I171F

PolyPhen 2 Score 0.224 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000135437
Gene: ENSMUSG00000078698
AA Change: I171F

Domain	Start	End	E-Value	Type
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

Meta Mutation Damage Score

0.1919

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.8%
20x: 93.3%

Validation Efficiency

98% (61/62)

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2510039O18Rik	T	C	4: 148,029,488 (GRCm39)	I486T	probably damaging	Het
4933427D14Rik	T	C	11: 72,089,567 (GRCm39)	R106G	probably damaging	Het
Cfap54	A	G	10: 92,675,333 (GRCm39)	S2863P	possibly damaging	Het
Copa	T	A	1: 171,948,812 (GRCm39)	S1155T	probably benign	Het
Crot	T	C	5: 9,027,541 (GRCm39)	T264A	probably benign	Het
Ddx3y	G	A	Y: 1,267,170 (GRCm39)	A232V	probably damaging	Het
Dst	T	G	1: 34,050,979 (GRCm39)	V25G	probably benign	Het
Ehbp1	C	T	11: 22,087,867 (GRCm39)	A406T	probably benign	Het
Eml5	A	T	12: 98,768,724 (GRCm39)		probably benign	Het
Eps8	A	T	6: 137,486,153 (GRCm39)	M453K	probably benign	Het
Galnt3	T	C	2: 65,937,374 (GRCm39)	D112G	possibly damaging	Het
Glra4	C	T	X: 135,663,542 (GRCm39)	A336T	probably damaging	Het
Gmppb	A	G	9: 107,927,338 (GRCm39)	D95G	probably benign	Het
Gprc6a	T	C	10: 51,504,544 (GRCm39)	Y100C	possibly damaging	Het
Gpx6	C	A	13: 21,501,828 (GRCm39)	S150Y	probably damaging	Het
Hsd17b3	A	T	13: 64,207,300 (GRCm39)	V247D	probably damaging	Het
Htr7	T	C	19: 36,034,160 (GRCm39)	D165G	probably damaging	Het
Igha	T	C	12: 113,219,972 (GRCm39)		probably benign	Het
Igsf10	A	G	3: 59,239,345 (GRCm39)	C279R	probably damaging	Het
Irak4	A	G	15: 94,452,621 (GRCm39)	E182G	possibly damaging	Het
Lipo3	A	T	19: 33,535,723 (GRCm39)	V274E	probably damaging	Het
Lrpprc	A	C	17: 85,078,269 (GRCm39)		probably null	Het
Mast1	T	C	8: 85,645,393 (GRCm39)	Y684C	probably damaging	Het
Mdn1	T	C	4: 32,722,363 (GRCm39)	F2382L	probably benign	Het
Mepe	C	T	5: 104,484,944 (GRCm39)	P28L	probably benign	Het
Muc2	T	A	7: 141,300,541 (GRCm39)		probably benign	Het
Myh3	C	T	11: 66,987,262 (GRCm39)	Q1371*	probably null	Het
Nodal	T	A	10: 61,258,833 (GRCm39)	V90E	probably benign	Het
Npas4	A	T	19: 5,036,579 (GRCm39)	H528Q	probably benign	Het
Nt5dc3	T	C	10: 86,660,100 (GRCm39)	V382A	probably damaging	Het
Pcdh18	G	A	3: 49,709,035 (GRCm39)	T293I	probably damaging	Het
Phf20l1	A	G	15: 66,513,665 (GRCm39)	D947G	probably damaging	Het
Phf8-ps	A	T	17: 33,285,405 (GRCm39)	S466T	probably benign	Het
Pla2r1	A	G	2: 60,279,306 (GRCm39)	V758A	probably benign	Het
Plod2	G	T	9: 92,480,672 (GRCm39)	G422*	probably null	Het
Ppp1r12a	T	C	10: 108,089,341 (GRCm39)	V660A	probably benign	Het
Prdm6	T	C	18: 53,673,278 (GRCm39)	I186T	possibly damaging	Het
Prkd3	G	A	17: 79,266,570 (GRCm39)		probably benign	Het
Prrc2a	A	G	17: 35,376,908 (GRCm39)	L734P	probably damaging	Het
Rnf128	C	A	X: 138,565,271 (GRCm39)	L282I	probably damaging	Het
Rnf213	A	G	11: 119,359,879 (GRCm39)	N4424S		Het
Scrn3	T	C	2: 73,166,121 (GRCm39)	S385P	possibly damaging	Het
Serpina1d	A	T	12: 103,734,107 (GRCm39)	S66T	probably benign	Het
Setd3	T	C	12: 108,131,417 (GRCm39)	K3R	possibly damaging	Het
Slc2a7	A	G	4: 150,242,667 (GRCm39)		probably null	Het
Smad4	G	T	18: 73,810,807 (GRCm39)	T59K	possibly damaging	Het
Spc25	A	G	2: 69,032,945 (GRCm39)	L60P	probably damaging	Het
Stam	A	C	2: 14,143,772 (GRCm39)	H354P	probably damaging	Het
Tesk1	C	T	4: 43,445,786 (GRCm39)	P280S	possibly damaging	Het
Tmem120a	C	G	5: 135,765,131 (GRCm39)	R254P	probably benign	Het
Traf5	T	C	1: 191,729,837 (GRCm39)	T405A	probably benign	Het
Trav7-4	A	G	14: 53,699,119 (GRCm39)	S89G	probably benign	Het
Tsc22d1	T	C	14: 76,656,049 (GRCm39)	S761P	probably damaging	Het
Ugt1a10	C	A	1: 88,143,862 (GRCm39)	H361N	probably damaging	Het
Ugt2b1	C	A	5: 87,065,534 (GRCm39)	V502L	probably benign	Het
Vip	T	A	10: 5,592,590 (GRCm39)	S77T	possibly damaging	Het
Wdr72	A	T	9: 74,125,979 (GRCm39)	M1025L	probably benign	Het
Zfp541	A	G	7: 15,806,147 (GRCm39)	D94G	probably damaging	Het

Other mutations in Mrgpra3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH 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
IGL03071:Mrgpra3	APN	7	47,238,929 (GRCm39)	utr 3 prime	probably benign
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
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

Predicted Primers

PCR Primer
(F):5'- AAACGGTCAGCATGATGGTC -3'
(R):5'- TCAAGTTTACCCTACCCAAAGG -3'

Sequencing Primer
(F):5'- GTCAGCATGATGGTCACGAATAATC -3'
(R):5'- TACCCTACCCAAAGGAATTTTTGC -3'

Posted On

2015-04-30