Mutagenetix > Incidental Mutation

Incidental Mutation 'R1835:Mrgpra3'

205168

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

039862-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.053) question?

Stock #

R1835 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

47588950-47601372 bp(-) (GRCm38)

Type of Mutation

nonsense

DNA Base Change (assembly)

G to T at 47589946 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Stop codon at position 77 (Y77*)

Ref Sequence

ENSEMBL: ENSMUSP00000135437 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000176369]

AlphaFold

no structure available at present

Predicted Effect

probably null
Transcript: ENSMUST00000176369
AA Change: Y77*

SMART Domains

Protein: ENSMUSP00000135437
Gene: ENSMUSG00000078698
AA Change: Y77*

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

Coding Region Coverage

1x: 97.4%
3x: 96.8%
10x: 94.9%
20x: 91.0%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 97 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2610507B11Rik	G	T	11: 78,287,750 (GRCm38)	V1993F	probably damaging	Het
4933425L06Rik	C	A	13: 105,082,194 (GRCm38)	A12E	unknown	Het
Acss2	T	A	2: 155,558,630 (GRCm38)	Y530N	probably damaging	Het
Adam4	T	C	12: 81,419,559 (GRCm38)	I763V	probably benign	Het
Aipl1	T	G	11: 72,030,499 (GRCm38)	K190T	possibly damaging	Het
Alms1	T	A	6: 85,678,503 (GRCm38)	S3344T	possibly damaging	Het
Alpi	A	G	1: 87,099,414 (GRCm38)	V381A	possibly damaging	Het
Ankfn1	A	T	11: 89,447,618 (GRCm38)	S365R	probably benign	Het
Aox2	G	A	1: 58,308,991 (GRCm38)	A623T	probably benign	Het
Apc	T	A	18: 34,317,077 (GRCm38)	L2308Q	probably damaging	Het
Atp9b	C	T	18: 80,778,883 (GRCm38)	V501I	probably benign	Het
Baz2b	T	C	2: 59,901,819 (GRCm38)	E1994G	probably benign	Het
Cacna1a	T	C	8: 84,581,357 (GRCm38)		probably null	Het
Cacna1h	C	A	17: 25,392,076 (GRCm38)	V583L	probably benign	Het
Cd55	T	C	1: 130,447,609 (GRCm38)		probably benign	Het
Cep192	T	A	18: 67,804,424 (GRCm38)	S75T	possibly damaging	Het
Cfap54	T	A	10: 92,962,375 (GRCm38)	D1674V	probably benign	Het
Churc1	T	C	12: 76,773,297 (GRCm38)	F27L	possibly damaging	Het
Coro1c	A	G	5: 113,848,543 (GRCm38)	I280T	probably benign	Het
Creb1	C	T	1: 64,550,950 (GRCm38)	Q32*	probably null	Het
Cyp2b9	A	G	7: 26,200,783 (GRCm38)	T339A	probably benign	Het
Dctn3	T	C	4: 41,720,813 (GRCm38)	R51G	probably damaging	Het
Ddb1	T	C	19: 10,626,593 (GRCm38)	V888A	probably damaging	Het
Disp1	A	G	1: 183,089,000 (GRCm38)	Y619H	probably damaging	Het
Dnajc9	T	C	14: 20,388,334 (GRCm38)	D96G	possibly damaging	Het
Eepd1	A	G	9: 25,482,868 (GRCm38)	T143A	possibly damaging	Het
Eps8	T	A	6: 137,522,279 (GRCm38)	K204*	probably null	Het
Ercc5	T	A	1: 44,180,875 (GRCm38)	S1102R	probably benign	Het
Ergic2	T	A	6: 148,189,581 (GRCm38)	Y211F	possibly damaging	Het
Fam135b	G	T	15: 71,490,711 (GRCm38)	L274M	probably damaging	Het
Fat3	G	A	9: 15,998,088 (GRCm38)	T2206I	probably damaging	Het
Fat4	A	G	3: 38,983,571 (GRCm38)	I3791V	probably benign	Het
Gemin4	A	G	11: 76,213,296 (GRCm38)	M213T	possibly damaging	Het
Gnai3	T	C	3: 108,118,407 (GRCm38)	M119V	probably benign	Het
Heatr5b	A	T	17: 78,773,563 (GRCm38)	L1420Q	probably damaging	Het
Herc2	G	T	7: 56,206,765 (GRCm38)	G3918*	probably null	Het
Ints9	A	G	14: 65,032,256 (GRCm38)	Y465C	probably damaging	Het
Ist1	A	G	8: 109,678,883 (GRCm38)	V175A	probably damaging	Het
Kcnj12	T	C	11: 61,069,557 (GRCm38)	L227P	possibly damaging	Het
Kcnq5	T	C	1: 21,466,387 (GRCm38)	S416G	probably benign	Het
Kdm3a	T	A	6: 71,613,956 (GRCm38)	T295S	probably benign	Het
Kif1c	T	A	11: 70,708,971 (GRCm38)	M479K	probably damaging	Het
Kif20b	T	C	19: 34,956,038 (GRCm38)	L83P	probably damaging	Het
Kndc1	A	G	7: 139,927,711 (GRCm38)	E1194G	probably damaging	Het
Llgl1	A	G	11: 60,704,730 (GRCm38)	M81V	probably benign	Het
Map4k5	C	A	12: 69,824,662 (GRCm38)	M495I	probably damaging	Het
Mest	C	T	6: 30,742,791 (GRCm38)	R146C	probably benign	Het
Mettl24	T	A	10: 40,737,816 (GRCm38)		probably null	Het
Mical1	T	C	10: 41,483,535 (GRCm38)	S586P	probably benign	Het
Mss51	A	T	14: 20,483,178 (GRCm38)	C408*	probably null	Het
Myh6	T	C	14: 54,957,401 (GRCm38)	T666A	probably benign	Het
Myo10	T	C	15: 25,805,587 (GRCm38)	C1685R	possibly damaging	Het
Naip5	A	T	13: 100,223,218 (GRCm38)	Y503*	probably null	Het
Neil1	A	C	9: 57,146,604 (GRCm38)	F144C	probably damaging	Het
Nipbl	T	A	15: 8,343,517 (GRCm38)	I1082F	possibly damaging	Het
Nkiras1	T	C	14: 18,276,732 (GRCm38)	V7A	probably damaging	Het
Ntng2	G	A	2: 29,197,057 (GRCm38)	Q384*	probably null	Het
Ocrl	T	A	X: 47,962,116 (GRCm38)	I74N	probably damaging	Het
Olfr137	A	T	17: 38,305,312 (GRCm38)	S50T	probably benign	Het
Olfr1385	A	T	11: 49,494,670 (GRCm38)	I46F	probably damaging	Het
Olfr1408	A	G	1: 173,130,815 (GRCm38)	V134A	probably benign	Het
Olfr381	A	C	11: 73,486,374 (GRCm38)	V150G	probably benign	Het
Olfr535	A	G	7: 140,492,709 (GRCm38)	S24G	probably benign	Het
Olfr761	C	T	17: 37,952,385 (GRCm38)	G213E	possibly damaging	Het
Patj	A	G	4: 98,491,590 (GRCm38)	D151G	probably benign	Het
Plpbp	T	C	8: 27,049,231 (GRCm38)	V126A	probably damaging	Het
Pold2	A	G	11: 5,873,454 (GRCm38)	L325P	possibly damaging	Het
Ppp1r12c	A	C	7: 4,483,651 (GRCm38)	S480A	probably damaging	Het
Pum1	T	C	4: 130,701,048 (GRCm38)	S124P	possibly damaging	Het
Pwp2	C	G	10: 78,179,091 (GRCm38)	G353A	probably damaging	Het
Reln	C	A	5: 21,979,002 (GRCm38)	Q1666H	probably damaging	Het
Rnf19a	T	C	15: 36,265,925 (GRCm38)	I9V	probably benign	Het
Ryr2	T	C	13: 11,769,878 (GRCm38)	H1063R	probably benign	Het
Samd14	C	G	11: 95,023,600 (GRCm38)	D361E	probably damaging	Het
Samd15	A	T	12: 87,201,843 (GRCm38)	N365I	probably damaging	Het
Sec16b	A	G	1: 157,531,312 (GRCm38)	H105R	probably benign	Het
Sez6	T	C	11: 77,953,503 (GRCm38)	S51P	probably benign	Het
Sh3bp1	T	A	15: 78,905,150 (GRCm38)	L236Q	probably damaging	Het
Sspo	C	T	6: 48,457,340 (GRCm38)	T991I	probably damaging	Het
Suco	A	T	1: 161,859,500 (GRCm38)	L97*	probably null	Het
Tab1	C	A	15: 80,148,296 (GRCm38)	R35S	probably benign	Het
Tet3	C	A	6: 83,404,163 (GRCm38)	S341I	possibly damaging	Het
Tlr1	A	T	5: 64,925,700 (GRCm38)	D511E	probably benign	Het
Tmem132b	A	C	5: 125,785,899 (GRCm38)	D656A	probably damaging	Het
Tmtc4	T	A	14: 122,941,988 (GRCm38)		probably null	Het
Trmo	T	C	4: 46,380,158 (GRCm38)	T404A	probably damaging	Het
Trpm1	A	G	7: 64,230,268 (GRCm38)	K790E	probably damaging	Het
Ulk4	C	A	9: 121,168,184 (GRCm38)	R774M	probably null	Het
Ush2a	C	T	1: 188,451,818 (GRCm38)	L1440F	probably benign	Het
Usp16	A	G	16: 87,480,907 (GRCm38)	K682E	probably damaging	Het
Virma	T	C	4: 11,540,511 (GRCm38)	S1471P	probably benign	Het
Vmn1r177	A	T	7: 23,865,686 (GRCm38)	I255N	probably damaging	Het
Vmn2r61	A	T	7: 42,266,652 (GRCm38)	R230*	probably null	Het
Vps13c	T	A	9: 67,993,013 (GRCm38)	F3671L	probably benign	Het
Washc5	T	C	15: 59,359,340 (GRCm38)	N358S	possibly damaging	Het
Wdr72	A	G	9: 74,151,617 (GRCm38)	K331E	probably damaging	Het
Zfp986	A	T	4: 145,899,235 (GRCm38)	K155I	probably benign	Het

Other mutations in Mrgpra3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00162:Mrgpra3	APN	7	47,589,519 (GRCm38)	missense	probably benign	0.00
IGL02097:Mrgpra3	APN	7	47,589,456 (GRCm38)	missense	possibly damaging	0.94
IGL02101:Mrgpra3	APN	7	47,589,552 (GRCm38)	missense	probably damaging	0.99
IGL03071:Mrgpra3	APN	7	47,589,181 (GRCm38)	utr 3 prime	probably benign
PIT4445001:Mrgpra3	UTSW	7	47,590,160 (GRCm38)	missense	possibly damaging	0.88
R0828:Mrgpra3	UTSW	7	47,590,136 (GRCm38)	missense	probably benign	0.12
R1118:Mrgpra3	UTSW	7	47,589,291 (GRCm38)	missense	possibly damaging	0.83
R2258:Mrgpra3	UTSW	7	47,590,094 (GRCm38)	missense	probably benign	0.35
R2393:Mrgpra3	UTSW	7	47,589,617 (GRCm38)	missense	possibly damaging	0.92
R3437:Mrgpra3	UTSW	7	47,589,566 (GRCm38)	missense	probably damaging	1.00
R3973:Mrgpra3	UTSW	7	47,589,666 (GRCm38)	missense	probably benign	0.22
R4273:Mrgpra3	UTSW	7	47,589,432 (GRCm38)	missense	probably benign	0.01
R4495:Mrgpra3	UTSW	7	47,590,065 (GRCm38)	missense	probably benign	0.00
R4768:Mrgpra3	UTSW	7	47,589,728 (GRCm38)	missense	possibly damaging	0.94
R4822:Mrgpra3	UTSW	7	47,589,968 (GRCm38)	missense	possibly damaging	0.69
R4967:Mrgpra3	UTSW	7	47,589,519 (GRCm38)	missense	probably benign	0.33
R5207:Mrgpra3	UTSW	7	47,590,161 (GRCm38)	missense	probably benign	0.06
R5569:Mrgpra3	UTSW	7	47,590,011 (GRCm38)	missense	probably benign	0.00
R5763:Mrgpra3	UTSW	7	47,589,607 (GRCm38)	nonsense	probably null
R6102:Mrgpra3	UTSW	7	47,590,149 (GRCm38)	missense	possibly damaging	0.92
R6612:Mrgpra3	UTSW	7	47,590,035 (GRCm38)	missense	probably benign	0.00
R6718:Mrgpra3	UTSW	7	47,589,696 (GRCm38)	missense	probably benign	0.25
R6859:Mrgpra3	UTSW	7	47,590,033 (GRCm38)	missense	probably benign	0.04
R7029:Mrgpra3	UTSW	7	47,589,542 (GRCm38)	missense	probably benign	0.00
R7034:Mrgpra3	UTSW	7	47,590,090 (GRCm38)	missense	possibly damaging	0.49
R7036:Mrgpra3	UTSW	7	47,590,090 (GRCm38)	missense	possibly damaging	0.49
R7097:Mrgpra3	UTSW	7	47,589,641 (GRCm38)	missense	probably benign
R7475:Mrgpra3	UTSW	7	47,589,947 (GRCm38)	missense	probably damaging	1.00
R8289:Mrgpra3	UTSW	7	47,589,720 (GRCm38)	missense	possibly damaging	0.76
R8315:Mrgpra3	UTSW	7	47,601,303 (GRCm38)	start codon destroyed	probably null	0.93
R9500:Mrgpra3	UTSW	7	47,589,652 (GRCm38)	nonsense	probably null
Z1177:Mrgpra3	UTSW	7	47,601,301 (GRCm38)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- AGTGATACCAGATGGGGCAC -3'
(R):5'- AACACCAGTGCAGGGTTTC -3'

Sequencing Primer
(F):5'- AGACAGGCAGCGCTCAGTG -3'
(R):5'- GGTTTCTGGCCCGAAACAC -3'

Posted On

2014-06-23