Mutagenetix > Incidental Mutation

Incidental Mutation 'R8158:Mrgpra1'

633363

Institutional Source

Beutler Lab

Gene Symbol

Mrgpra1

Ensembl Gene

ENSMUSG00000050650

Gene Name

MAS-related GPR, member A1

Synonyms

MrgA1

MMRRC Submission

067584-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.070) question?

Stock #

R8158 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

46984623-47003988 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 46985204 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Stop codon at position 158 (C158*)

Ref Sequence

ENSEMBL: ENSMUSP00000129978 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000098438]

AlphaFold

no structure available at present

Predicted Effect

probably null
Transcript: ENSMUST00000098438
AA Change: C158*

SMART Domains

Protein: ENSMUSP00000129978
Gene: ENSMUSG00000050650
AA Change: C158*

Domain	Start	End	E-Value	Type
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

1x: 100.0%
3x: 99.9%
10x: 99.5%
20x: 98.3%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abl2	T	A	1: 156,469,639 (GRCm39)	S968T	probably benign	Het
Adcy8	T	C	15: 64,655,655 (GRCm39)	D608G	probably benign	Het
Adgb	C	T	10: 10,254,478 (GRCm39)	V1162M	probably benign	Het
Agrn	A	G	4: 156,258,346 (GRCm39)	V1040A	probably benign	Het
Amer3	A	T	1: 34,626,741 (GRCm39)	T327S	possibly damaging	Het
Apaf1	C	T	10: 90,895,520 (GRCm39)	C426Y	probably benign	Het
Bsn	T	C	9: 107,987,232 (GRCm39)	D2840G	unknown	Het
Camsap1	A	T	2: 25,834,440 (GRCm39)	C406*	probably null	Het
Cbr2	A	T	11: 120,621,123 (GRCm39)	M158K	probably damaging	Het
Cgrrf1	T	C	14: 47,091,192 (GRCm39)	S239P	probably benign	Het
Clnk	C	A	5: 38,952,254 (GRCm39)		probably null	Het
Csad	T	C	15: 102,086,197 (GRCm39)	M445V	probably damaging	Het
Dnajb7	T	A	15: 81,291,600 (GRCm39)	N246Y	probably damaging	Het
Dok6	T	C	18: 89,492,071 (GRCm39)	I169V	probably benign	Het
H2bc14	T	C	13: 21,906,631 (GRCm39)	Y122H	probably benign	Het
Il1f10	T	G	2: 24,181,267 (GRCm39)	I11R	possibly damaging	Het
Irs1	C	T	1: 82,267,254 (GRCm39)	V321M	probably damaging	Het
Itga9	T	C	9: 118,706,211 (GRCm39)	F938L	probably damaging	Het
Kif7	T	C	7: 79,354,442 (GRCm39)	D781G	probably damaging	Het
Klhl41	A	T	2: 69,501,505 (GRCm39)	N322I	probably damaging	Het
Krtap31-1	T	G	11: 99,798,901 (GRCm39)	C35G	possibly damaging	Het
Lsm11	A	T	11: 45,824,824 (GRCm39)	D234E	probably benign	Het
Med6	T	C	12: 81,620,677 (GRCm39)	K223R	probably benign	Het
Mfsd4b2	G	A	10: 39,798,064 (GRCm39)	T97I	probably benign	Het
Nr2e1	T	C	10: 42,458,881 (GRCm39)	T8A	probably benign	Het
Oas2	T	C	5: 120,887,838 (GRCm39)	M1V	probably null	Het
Or13a27	T	C	7: 139,925,162 (GRCm39)	I247V	probably benign	Het
Or14a260	T	A	7: 85,984,885 (GRCm39)	I240F	probably benign	Het
Or1e33	T	A	11: 73,738,697 (GRCm39)	M85L	probably benign	Het
Or8k17	T	C	2: 86,066,504 (GRCm39)	Y218C	probably damaging	Het
Or8w1	T	A	2: 87,465,233 (GRCm39)	N286I	probably damaging	Het
Otof	C	T	5: 30,537,538 (GRCm39)	G1257D	probably benign	Het
Phf2	T	C	13: 48,971,236 (GRCm39)	T479A	probably benign	Het
Pik3c2a	T	C	7: 115,942,232 (GRCm39)	N1516S	probably benign	Het
Qrich1	C	A	9: 108,433,236 (GRCm39)	T622K	probably damaging	Het
Rasip1	A	G	7: 45,281,943 (GRCm39)	K482R	probably damaging	Het
Rgl2	T	C	17: 34,155,918 (GRCm39)	F698L	probably benign	Het
Scarb1	T	C	5: 125,380,201 (GRCm39)	D124G	probably benign	Het
Sclt1	A	G	3: 41,625,917 (GRCm39)	I350T	probably benign	Het
Sec23ip	T	G	7: 128,369,364 (GRCm39)	V696G	probably damaging	Het
Serpina1e	G	T	12: 103,917,354 (GRCm39)	T105K	probably benign	Het
Sin3a	A	G	9: 57,020,828 (GRCm39)		probably null	Het
Slc34a2	A	G	5: 53,218,182 (GRCm39)	T154A	probably damaging	Het
Slc9a3	T	C	13: 74,303,241 (GRCm39)	L178P	probably damaging	Het
Smarca2	A	C	19: 26,659,448 (GRCm39)	I913L	probably benign	Het
Spaca7b	T	A	8: 11,715,056 (GRCm39)	D46V	probably damaging	Het
Tcea3	G	A	4: 136,001,027 (GRCm39)		probably null	Het
Tektl1	G	C	10: 78,584,509 (GRCm39)	Q338E	probably benign	Het
Tmcc1	T	A	6: 116,020,435 (GRCm39)	H339L		Het
Trpm2	G	T	10: 77,783,731 (GRCm39)	H247Q	probably damaging	Het
Tyr	T	A	7: 87,121,724 (GRCm39)	D356V	probably damaging	Het
Vmn2r54	A	T	7: 12,349,888 (GRCm39)	C565S	probably damaging	Het
Vmn2r82	A	C	10: 79,213,636 (GRCm39)	N74T	probably benign	Het
Zcchc4	T	C	5: 52,973,260 (GRCm39)	Y375H	probably damaging	Het
Zfhx3	T	A	8: 109,675,353 (GRCm39)	D2134E	possibly damaging	Het
Zfhx4	T	A	3: 5,464,010 (GRCm39)	Y1414*	probably null	Het
Zfp282	A	T	6: 47,867,626 (GRCm39)	E267D	possibly damaging	Het
Zfp442	A	T	2: 150,251,096 (GRCm39)	C269S	possibly damaging	Het
Zp3	T	A	5: 136,014,418 (GRCm39)	S246T	probably benign	Het

Other mutations in Mrgpra1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00903:Mrgpra1	APN	7	46,985,326 (GRCm39)	missense	probably benign	0.00
IGL01317:Mrgpra1	APN	7	46,985,372 (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
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

Predicted Primers

PCR Primer
(F):5'- AGCTTTATCTGCCCAGTACCAC -3'
(R):5'- AGGAACGCCTTCTCAGTCTAC -3'

Sequencing Primer
(F):5'- TTTATCTGCCCAGTACCACAGAAC -3'
(R):5'- GGTCACATCATAGATTCCATACTGC -3'

Posted On

2020-06-30