Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03337:Gm6455'

417064

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm6455

Ensembl Gene

Gene Name

predicted gene 6455

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL03337

Quality Score

Status

Chromosome

Chromosomal Location

10914996-10920775 bp(+) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

A to G at 10917251 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000095015

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000168057

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000198483

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 22 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca15	A	G	7: 119,995,930 (GRCm39)	I1356V	probably benign	Het
Akr1b8	T	C	6: 34,331,209 (GRCm39)	I15T	probably benign	Het
Arrdc3	G	A	13: 81,038,766 (GRCm39)	V23I	probably benign	Het
Bmp6	G	A	13: 38,682,919 (GRCm39)	V470I	probably damaging	Het
Cltc	A	T	11: 86,594,509 (GRCm39)	I1476N	possibly damaging	Het
Dclk2	A	C	3: 86,813,366 (GRCm39)	I193M	probably damaging	Het
Dnah5	A	G	15: 28,290,287 (GRCm39)	M1226V	probably benign	Het
Firrm	A	G	1: 163,818,328 (GRCm39)	S38P	probably damaging	Het
Igkv4-62	A	T	6: 69,376,946 (GRCm39)	W68R	probably damaging	Het
Lbr	C	T	1: 181,659,788 (GRCm39)	G136R	possibly damaging	Het
Ldhb	C	T	6: 142,439,882 (GRCm39)	M219I	probably benign	Het
Lysmd2	A	G	9: 75,542,945 (GRCm39)	D184G	probably damaging	Het
Nrxn3	T	A	12: 89,221,790 (GRCm39)	M150K	probably damaging	Het
Pdss2	T	C	10: 43,221,589 (GRCm39)	V167A	probably damaging	Het
Scn7a	A	T	2: 66,506,304 (GRCm39)	D1528E	probably benign	Het
Thsd7a	C	T	6: 12,405,173 (GRCm39)	C757Y	probably damaging	Het
Tmem213	T	C	6: 38,086,478 (GRCm39)		probably null	Het
Trip11	A	G	12: 101,851,278 (GRCm39)	S929P	probably damaging	Het
Utp20	T	A	10: 88,590,428 (GRCm39)	M2349L	probably benign	Het
Vmn2r58	T	A	7: 41,513,810 (GRCm39)	I278F	possibly damaging	Het
Vmn2r61	A	G	7: 41,916,509 (GRCm39)	N374S	possibly damaging	Het
Vps8	A	G	16: 21,381,918 (GRCm39)	T1089A	probably benign	Het

Other mutations in Gm6455

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02408:Gm6455	APN	5	10,917,257 (GRCm39)	exon	noncoding transcript

Posted On

2016-08-02