Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03272:Gpr141b'

415304

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 #

IGL03272

Quality Score

Status

Chromosome

Chromosomal Location

19911596-19917121 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

A to T at 19913707 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: 24 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acp2	C	T	2: 91,034,578 (GRCm39)		probably benign	Het
B4galnt3	T	C	6: 120,193,267 (GRCm39)	D413G	probably damaging	Het
Chd2	T	C	7: 73,102,914 (GRCm39)	D1357G	possibly damaging	Het
Dsg1b	T	C	18: 20,530,446 (GRCm39)	L367P	probably benign	Het
Emsy	A	T	7: 98,242,969 (GRCm39)	F1057I	probably damaging	Het
Fam171a2	A	T	11: 102,334,944 (GRCm39)	F64L	possibly damaging	Het
Fat4	T	C	3: 39,063,852 (GRCm39)	S4603P	probably benign	Het
Fyco1	T	C	9: 123,658,668 (GRCm39)	T503A	probably benign	Het
Gpr179	T	C	11: 97,227,419 (GRCm39)	T1579A	possibly damaging	Het
Itgae	T	C	11: 73,024,680 (GRCm39)		probably null	Het
Lrriq3	A	T	3: 154,806,695 (GRCm39)	I115F	probably damaging	Het
Mmrn1	A	G	6: 60,965,419 (GRCm39)	D1149G	probably damaging	Het
Mylk	A	C	16: 34,799,559 (GRCm39)	K1650Q	probably benign	Het
Nrap	T	C	19: 56,334,000 (GRCm39)		probably benign	Het
Or5h25	A	C	16: 58,930,919 (GRCm39)	V18G	probably benign	Het
Ovgp1	T	A	3: 105,888,641 (GRCm39)	D332E	probably damaging	Het
Pou2f1	A	T	1: 165,724,049 (GRCm39)	I296K	possibly damaging	Het
Psd4	A	G	2: 24,295,692 (GRCm39)		probably benign	Het
Satb2	T	C	1: 56,884,802 (GRCm39)	Q433R	probably damaging	Het
Serpinb9f	A	T	13: 33,511,899 (GRCm39)	N134I	probably damaging	Het
Slc6a3	A	G	13: 73,689,048 (GRCm39)	N124S	probably damaging	Het
Spta1	A	G	1: 174,041,710 (GRCm39)	N1360S	probably benign	Het
Strc	G	A	2: 121,202,232 (GRCm39)	T1212I	probably damaging	Het
Tmtc3	T	C	10: 100,292,942 (GRCm39)	K472R	probably benign	Het

Other mutations in Gpr141b

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL02834:Gpr141b	APN	13	19,914,045 (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

2016-08-02