Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01749:Gm5263'

278816

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm5263

Ensembl Gene

Gene Name

predicted gene 5263

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01749

Quality Score

Status

Chromosome

Chromosomal Location

146296174-146296774 bp(+) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

T to G at 146296302 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: ENSMUST00000163646

SMART Domains

Protein: ENSMUSP00000126089
Gene: ENSMUSG00000090323

Domain	Start	End	E-Value	Type
PDB:2RR6\|A	1	111	6e-46	PDB
SCOP:d1a9na_	20	119	4e-7	SMART
Blast:AAA	23	92	6e-11	BLAST

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000186665

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
Abca6	T	C	11: 110,135,050 (GRCm39)	E245G	probably damaging	Het
Bach2	A	G	4: 32,580,261 (GRCm39)	T829A	probably damaging	Het
Car1	T	A	3: 14,832,519 (GRCm39)	H205L	probably benign	Het
Cmya5	T	C	13: 93,225,807 (GRCm39)	T3094A	probably benign	Het
Dctn2	G	A	10: 127,117,286 (GRCm39)	R380H	possibly damaging	Het
Flt3	T	C	5: 147,294,838 (GRCm39)	K411R	probably benign	Het
Hook2	T	C	8: 85,719,865 (GRCm39)		probably null	Het
Iqsec1	G	A	6: 90,657,486 (GRCm39)	R571C	probably benign	Het
Lig3	T	G	11: 82,680,693 (GRCm39)	L421R	probably damaging	Het
Mtcl2	G	T	2: 156,863,461 (GRCm39)		probably benign	Het
Nipbl	A	G	15: 8,391,305 (GRCm39)	V223A	probably benign	Het
Or2n1	G	T	17: 38,486,577 (GRCm39)	V201L	probably benign	Het
Or2y12	A	T	11: 49,426,944 (GRCm39)	R311W	probably damaging	Het
Or8b48	C	T	9: 38,492,809 (GRCm39)	P79S	probably damaging	Het
Reln	C	A	5: 22,549,244 (GRCm39)	E55*	probably null	Het
Tlr1	A	T	5: 65,083,290 (GRCm39)	L429*	probably null	Het
Ttc22	A	G	4: 106,495,800 (GRCm39)	T385A	probably benign	Het
Vmn1r48	A	G	6: 90,012,934 (GRCm39)	V297A	possibly damaging	Het

Other mutations in Gm5263

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01750:Gm5263	APN	1	146,296,302 (GRCm39)	exon	noncoding transcript
IGL01751:Gm5263	APN	1	146,296,302 (GRCm39)	exon	noncoding transcript
IGL01767:Gm5263	APN	1	146,296,302 (GRCm39)	exon	noncoding transcript
IGL01810:Gm5263	APN	1	146,296,292 (GRCm39)	exon	noncoding transcript

Posted On

2015-04-16