Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01763:Gm5611'

153607

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm5611

Ensembl Gene

ENSMUSG00000090602

Gene Name

predicted gene 5611

Synonyms

Accession Numbers

Essential gene?

Probably essential (E-score: 0.964) question?

Stock #

IGL01763

Quality Score

Status

Chromosome

Chromosomal Location

16941341-16942192 bp(+) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

A to G at 16941699 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000164523

SMART Domains

Protein: ENSMUSP00000130546
Gene: ENSMUSG00000090602

Domain	Start	End	E-Value	Type
Pfam:Nucleoplasmin	12	173	7.7e-64	PFAM
low complexity region	207	219	N/A	INTRINSIC
Pfam:NPM1-C	223	271	8.1e-38	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 27 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acer3	C	T	7: 97,915,339 (GRCm39)		probably benign	Het
Atp4a	A	G	7: 30,414,943 (GRCm39)	E244G	probably benign	Het
Cdh20	T	C	1: 109,993,520 (GRCm39)	I325T	probably benign	Het
Dennd2c	T	C	3: 103,064,224 (GRCm39)	L623P	probably damaging	Het
Eef1akmt3	T	C	10: 126,876,952 (GRCm39)	D65G	probably benign	Het
Gimap3	T	A	6: 48,742,430 (GRCm39)	S167C	probably damaging	Het
Gm12185	A	T	11: 48,806,671 (GRCm39)	F173L	probably benign	Het
Gpr161	T	C	1: 165,144,820 (GRCm39)	S387P	probably benign	Het
Hsd17b8	A	G	17: 34,245,835 (GRCm39)	V219A	probably damaging	Het
Mtfr2	G	A	10: 20,228,683 (GRCm39)		probably benign	Het
Myh8	A	G	11: 67,177,245 (GRCm39)	K437R	probably benign	Het
Myo15a	A	G	11: 60,412,564 (GRCm39)	D3335G	probably benign	Het
Ndufaf7	C	T	17: 79,253,771 (GRCm39)	T323I	possibly damaging	Het
Or5g29	A	G	2: 85,421,691 (GRCm39)	N269S	probably benign	Het
Pcdh15	T	C	10: 74,046,293 (GRCm39)	V190A	probably benign	Het
Pdzd2	A	G	15: 12,372,632 (GRCm39)	V2501A	probably benign	Het
Piwil4	A	T	9: 14,617,562 (GRCm39)		probably null	Het
Plxnb2	C	T	15: 89,046,184 (GRCm39)		probably null	Het
Sgcd	A	G	11: 47,085,856 (GRCm39)		probably null	Het
Sin3b	A	G	8: 73,473,236 (GRCm39)	K519E	probably damaging	Het
Slc26a4	C	T	12: 31,578,853 (GRCm39)		probably benign	Het
Spty2d1	T	C	7: 46,649,596 (GRCm39)	D33G	probably damaging	Het
Txnrd3	C	T	6: 89,638,537 (GRCm39)	T242I	probably damaging	Het
Vps13b	A	G	15: 35,709,945 (GRCm39)	D1964G	possibly damaging	Het
Wdr24	A	G	17: 26,045,164 (GRCm39)	T300A	probably benign	Het
Zc2hc1c	C	A	12: 85,336,450 (GRCm39)	Q36K	probably benign	Het
Zfp719	A	T	7: 43,233,613 (GRCm39)	I11F	probably benign	Het

Other mutations in Gm5611

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01615:Gm5611	APN	9	16,941,647 (GRCm39)	exon	noncoding transcript
IGL01800:Gm5611	APN	9	16,941,767 (GRCm39)	exon	noncoding transcript
R1536:Gm5611	UTSW	9	16,941,903 (GRCm39)	exon	noncoding transcript
R1830:Gm5611	UTSW	9	16,942,073 (GRCm39)	exon	noncoding transcript
R4111:Gm5611	UTSW	9	16,941,989 (GRCm39)	exon	noncoding transcript
R4113:Gm5611	UTSW	9	16,941,989 (GRCm39)	exon	noncoding transcript

Posted On

2014-02-04