Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00764:4930480E11Rik'

8465

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

4930480E11Rik

Ensembl Gene

Gene Name

RIKEN cDNA 4930480E11 gene

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.050) question?

Stock #

IGL00764

Quality Score

Status

Chromosome

Chromosomal Location

77413249-77414734 bp(+) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

C to T at 77413625 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Stop codon at position 117 (Q117*)

Ref Sequence

ENSEMBL: ENSMUSP00000037594 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000035626]

Predicted Effect

probably null
Transcript: ENSMUST00000035626
AA Change: Q117*

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 18 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Cep350	G	T	1: 155,816,492 (GRCm39)	T401K	possibly damaging	Het
Dnah17	A	G	11: 117,987,311 (GRCm39)	V1333A	probably damaging	Het
Dnah6	T	C	6: 73,172,603 (GRCm39)	N285S	possibly damaging	Het
Eif2b3	T	C	4: 116,923,666 (GRCm39)	S294P	probably benign	Het
Fanci	A	G	7: 79,045,660 (GRCm39)	M1V	probably null	Het
Fgd6	A	G	10: 93,879,496 (GRCm39)	I117V	probably benign	Het
Fgf15	A	G	7: 144,450,672 (GRCm39)		probably null	Het
Iars1	T	C	13: 49,865,303 (GRCm39)	I593T	probably benign	Het
Myof	A	T	19: 37,963,371 (GRCm39)	C409S	probably benign	Het
Nedd1	A	T	10: 92,530,836 (GRCm39)		probably benign	Het
Neto1	A	T	18: 86,516,937 (GRCm39)	H418L	probably damaging	Het
Plxnd1	A	T	6: 115,944,933 (GRCm39)	V981E	possibly damaging	Het
Ptpn13	T	C	5: 103,745,584 (GRCm39)	V2430A	probably damaging	Het
Thbs2	G	T	17: 14,910,514 (GRCm39)	D28E	probably damaging	Het
Vps50	C	T	6: 3,532,177 (GRCm39)	Q227*	probably null	Het
Xpnpep2	T	C	X: 47,220,031 (GRCm39)	V604A	probably benign	Het
Zfp773	T	G	7: 7,135,683 (GRCm39)	K304N	probably damaging	Het
Zfp831	A	G	2: 174,487,701 (GRCm39)	E792G	possibly damaging	Het

Other mutations in 4930480E11Rik

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R2888:4930480E11Rik	UTSW	X	77,414,288 (GRCm39)	missense	probably damaging	0.99
R2889:4930480E11Rik	UTSW	X	77,414,288 (GRCm39)	missense	probably damaging	0.99
R2890:4930480E11Rik	UTSW	X	77,414,288 (GRCm39)	missense	probably damaging	0.99
R2897:4930480E11Rik	UTSW	X	77,413,868 (GRCm39)	nonsense	probably null
R2898:4930480E11Rik	UTSW	X	77,413,868 (GRCm39)	nonsense	probably null
R7117:4930480E11Rik	UTSW	X	77,414,311 (GRCm39)	missense	probably benign	0.24
R7250:4930480E11Rik	UTSW	X	77,414,311 (GRCm39)	missense	probably benign	0.24
R7251:4930480E11Rik	UTSW	X	77,414,311 (GRCm39)	missense	probably benign	0.24
R7252:4930480E11Rik	UTSW	X	77,414,311 (GRCm39)	missense	probably benign	0.24

Posted On

2012-12-06