Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00563:AU016765'

332619

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

AU016765

Ensembl Gene

ENSMUSG00000073377

Gene Name

expressed sequence AU016765

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.123) question?

Stock #

IGL00563

Quality Score

Status

Chromosome

Chromosomal Location

64821084-64862585 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

C to A at 64826877 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: ENSMUST00000097295

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000168379

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000168920

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000169472

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
1500035N22Rik	T	C	5: 25,202,619 (GRCm39)		probably benign	Het
Atp13a4	T	C	16: 29,222,596 (GRCm39)		probably benign	Het
Clstn2	A	G	9: 97,464,505 (GRCm39)		probably benign	Het
Crip1	T	A	12: 113,117,232 (GRCm39)		probably null	Het
Dnah6	T	C	6: 73,172,603 (GRCm39)	N285S	possibly damaging	Het
Fktn	A	T	4: 53,747,007 (GRCm39)		probably null	Het
Fndc3a	C	A	14: 72,796,797 (GRCm39)		probably benign	Het
Focad	T	A	4: 88,267,046 (GRCm39)	M1019K	unknown	Het
Fuca2	A	T	10: 13,381,651 (GRCm39)	D188V	probably damaging	Het
Gzmk	C	T	13: 113,309,658 (GRCm39)	V92I	probably benign	Het
Mprip	C	T	11: 59,643,443 (GRCm39)	R520W	probably damaging	Het
Mrpl19	A	G	6: 81,942,853 (GRCm39)	V19A	probably benign	Het
Ndufb3	T	A	1: 58,634,958 (GRCm39)	H103Q	possibly damaging	Het
Pkd1l3	T	C	8: 110,382,779 (GRCm39)	V1675A	possibly damaging	Het
Saxo1	C	T	4: 86,363,809 (GRCm39)	E225K	probably damaging	Het
Sbno1	A	G	5: 124,540,268 (GRCm39)	S383P	probably damaging	Het
Slc22a29	T	A	19: 8,138,993 (GRCm39)	T490S	probably benign	Het
Smc6	T	A	12: 11,351,532 (GRCm39)	S854T	probably benign	Het
Smim23	T	C	11: 32,771,893 (GRCm39)	T58A	probably benign	Het
Tas2r134	T	C	2: 51,518,100 (GRCm39)	I193T	possibly damaging	Het
Thsd7a	G	T	6: 12,379,658 (GRCm39)		probably null	Het
Trav13n-4	T	G	14: 53,601,423 (GRCm39)	V64G	possibly damaging	Het
Trmt10a	G	A	3: 137,853,177 (GRCm39)	E13K	probably damaging	Het
Txndc11	T	C	16: 10,922,496 (GRCm39)	S239G	probably damaging	Het
Vmn2r96	T	A	17: 18,804,077 (GRCm39)	N442K	probably benign	Het
Vps13a	C	T	19: 16,712,078 (GRCm39)		probably null	Het
Wdr64	A	G	1: 175,526,366 (GRCm39)	D5G	probably benign	Het

Other mutations in AU016765

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL00562:AU016765	APN	17	64,826,877 (GRCm39)	exon	noncoding transcript
R1718:AU016765	UTSW	17	64,862,433 (GRCm39)	exon	noncoding transcript
R1936:AU016765	UTSW	17	64,826,873 (GRCm39)	exon	noncoding transcript
R1940:AU016765	UTSW	17	64,826,873 (GRCm39)	exon	noncoding transcript
R2140:AU016765	UTSW	17	64,826,995 (GRCm39)	exon	noncoding transcript
R4665:AU016765	UTSW	17	64,826,916 (GRCm39)	exon	noncoding transcript

Posted On

2015-08-05