Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02834:Gpr141b'

361574

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gpr141b

Ensembl Gene

Gene Name

G protein-coupled receptor 141B

Synonyms

Karma, A530099J19Rik

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL02834

Quality Score

Status

Chromosome

Chromosomal Location

19911596-19917121 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

A to T at 19914045 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000151029

SMART Domains

Protein: ENSMUSP00000133733
Gene: ENSMUSG00000047462

Domain	Start	End	E-Value	Type
Pfam:7tm_1	46	294	3.8e-7	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 26 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Arhgap10	A	T	8: 78,091,729 (GRCm39)	L430Q	probably damaging	Het
Cc2d2a	C	T	5: 43,871,863 (GRCm39)	R900*	probably null	Het
Cd14	A	G	18: 36,858,556 (GRCm39)	Y300H	probably benign	Het
Dgcr8	T	A	16: 18,090,623 (GRCm39)	T584S	probably benign	Het
Epb41l5	C	T	1: 119,551,685 (GRCm39)	G100D	probably benign	Het
Fat4	G	A	3: 39,010,893 (GRCm39)	G1998R	probably damaging	Het
Fndc3b	A	T	3: 27,562,652 (GRCm39)	L279H	probably damaging	Het
Gabrr1	A	G	4: 33,151,426 (GRCm39)	E114G	probably damaging	Het
Hrh2	A	G	13: 54,369,019 (GRCm39)	R332G	probably benign	Het
Kif5a	T	C	10: 127,081,625 (GRCm39)	I180V	probably benign	Het
Lyg2	T	A	1: 37,949,048 (GRCm39)	R105W	probably damaging	Het
Myc	A	G	15: 61,859,515 (GRCm39)	I64V	probably damaging	Het
Nrcam	G	A	12: 44,587,858 (GRCm39)		probably null	Het
Ogdhl	A	G	14: 32,047,903 (GRCm39)	Y51C	probably damaging	Het
Or13p5	C	T	4: 118,591,803 (GRCm39)	L26F	probably benign	Het
Or51m1	T	A	7: 103,578,601 (GRCm39)	C190*	probably null	Het
Pdlim3	A	G	8: 46,370,569 (GRCm39)	R290G	probably benign	Het
Ppm1l	G	A	3: 69,456,676 (GRCm39)	A198T	probably damaging	Het
Prkd2	A	G	7: 16,579,859 (GRCm39)	D119G	probably damaging	Het
Rapgef3	A	T	15: 97,646,146 (GRCm39)	I820N	probably damaging	Het
Scnn1b	A	G	7: 121,511,285 (GRCm39)	Y324C	probably damaging	Het
Smc5	G	A	19: 23,234,968 (GRCm39)	R289C	probably benign	Het
Vmn2r51	T	A	7: 9,832,063 (GRCm39)	R508*	probably null	Het
Vps13c	A	T	9: 67,845,137 (GRCm39)	I2074L	probably benign	Het
Wdr64	T	C	1: 175,633,415 (GRCm39)		probably benign	Het
Ydjc	C	T	16: 16,965,153 (GRCm39)	P74L	probably benign	Het

Other mutations in Gpr141b

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL03272:Gpr141b	APN	13	19,913,707 (GRCm39)	exon	noncoding transcript
R0383:Gpr141b	UTSW	13	19,913,317 (GRCm39)	exon	noncoding transcript
R0401:Gpr141b	UTSW	13	19,913,664 (GRCm39)	exon	noncoding transcript
R1564:Gpr141b	UTSW	13	19,913,470 (GRCm39)	exon	noncoding transcript
R1800:Gpr141b	UTSW	13	19,913,849 (GRCm39)	exon	noncoding transcript
R3964:Gpr141b	UTSW	13	19,913,614 (GRCm39)	exon	noncoding transcript
R3966:Gpr141b	UTSW	13	19,913,614 (GRCm39)	exon	noncoding transcript
R4091:Gpr141b	UTSW	13	19,913,635 (GRCm39)	exon	noncoding transcript
R4832:Gpr141b	UTSW	13	19,913,840 (GRCm39)	exon	noncoding transcript
R5671:Gpr141b	UTSW	13	19,913,465 (GRCm39)	exon	noncoding transcript
R5885:Gpr141b	UTSW	13	19,913,519 (GRCm39)	exon	noncoding transcript
R5932:Gpr141b	UTSW	13	19,913,646 (GRCm39)	exon	noncoding transcript
R5956:Gpr141b	UTSW	13	19,913,300 (GRCm39)	exon	noncoding transcript
X0026:Gpr141b	UTSW	13	19,913,171 (GRCm39)	exon	noncoding transcript
Z1088:Gpr141b	UTSW	13	19,913,379 (GRCm39)	exon	noncoding transcript

Posted On

2015-12-18