Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01750:Gm5263'

278821

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm5263

Ensembl Gene

ENSMUSG00000090323

Gene Name

predicted gene 5263

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01750

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):

AlphaFold

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: 29 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Alpk3	A	G	7: 80,742,030 (GRCm39)	R616G	probably damaging	Het
Cacna1b	G	A	2: 24,544,407 (GRCm39)	P1260S	probably damaging	Het
Ccz1	A	T	5: 143,940,880 (GRCm39)	Y225N	probably damaging	Het
Col15a1	C	T	4: 47,303,897 (GRCm39)	P1101S	probably damaging	Het
Cyp2d22	T	A	15: 82,258,570 (GRCm39)	H97L	probably benign	Het
Emsy	G	A	7: 98,268,508 (GRCm39)	S511F	probably damaging	Het
Fnbp1l	G	T	3: 122,338,326 (GRCm39)	Y351*	probably null	Het
Hook2	T	C	8: 85,719,865 (GRCm39)		probably null	Het
Hrob	T	C	11: 102,145,777 (GRCm39)		probably benign	Het
Itgb4	G	A	11: 115,879,752 (GRCm39)	V635I	probably damaging	Het
Kmt2d	G	A	15: 98,751,049 (GRCm39)		probably benign	Het
Lpin1	T	C	12: 16,627,177 (GRCm39)	N123S	probably benign	Het
Man2c1	T	C	9: 57,048,064 (GRCm39)		probably null	Het
Obscn	T	C	11: 58,922,465 (GRCm39)	E6558G	probably damaging	Het
Or2j6	T	C	7: 139,980,570 (GRCm39)	T130A	probably benign	Het
Or2n1	G	T	17: 38,486,577 (GRCm39)	V201L	probably benign	Het
Or8b48	C	T	9: 38,492,809 (GRCm39)	P79S	probably damaging	Het
Pcdh7	A	G	5: 57,877,764 (GRCm39)	T440A	probably damaging	Het
Pitx1	A	G	13: 55,974,304 (GRCm39)	Y176H	probably damaging	Het
Plec	A	G	15: 76,057,589 (GRCm39)	V4116A	probably damaging	Het
Polrmt	A	G	10: 79,575,680 (GRCm39)	V617A	possibly damaging	Het
Pprc1	T	C	19: 46,060,268 (GRCm39)		probably benign	Het
Rbm19	G	A	5: 120,256,857 (GRCm39)	A57T	probably benign	Het
Rin1	T	C	19: 5,102,064 (GRCm39)	I134T	possibly damaging	Het
Thumpd2	G	A	17: 81,361,815 (GRCm39)	A137V	probably benign	Het
Tle4	T	C	19: 14,427,153 (GRCm39)	Y756C	probably damaging	Het
Tln1	A	G	4: 43,545,435 (GRCm39)	L986P	probably damaging	Het
Tmem132c	C	A	5: 127,540,023 (GRCm39)	Q350K	possibly damaging	Het
Zfp474	A	G	18: 52,772,349 (GRCm39)	N334S	possibly damaging	Het

Other mutations in Gm5263

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01749: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