Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01077:Gm53'

52237

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm53

Ensembl Gene

ENSMUSG00000078706

Gene Name

predicted gene 53

Synonyms

LOC193022

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.088) question?

Stock #

IGL01077

Quality Score

Status

Chromosome

Chromosomal Location

96142486-96155310 bp(+) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

C to T at 96142594 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: ENSMUST00000119837

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000129907

SMART Domains

Protein: ENSMUSP00000119642
Gene: ENSMUSG00000078706

Domain	Start	End	E-Value	Type
low complexity region	3	14	N/A	INTRINSIC
low complexity region	20	36	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000139381

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000150490

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 28 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aox1	A	T	1: 58,096,569 (GRCm39)		probably benign	Het
Arhgap4	A	G	X: 72,943,699 (GRCm39)		probably benign	Het
Ascc3	T	G	10: 50,525,413 (GRCm39)		probably benign	Het
Cacng5	C	T	11: 107,772,531 (GRCm39)	V106I	probably benign	Het
Car10	T	C	11: 93,487,969 (GRCm39)	I222T	possibly damaging	Het
Cep250	G	A	2: 155,804,054 (GRCm39)	V55M	probably damaging	Het
Chst4	T	A	8: 110,756,597 (GRCm39)	Y422F	probably benign	Het
Dnajc13	T	C	9: 104,108,220 (GRCm39)	E185G	probably benign	Het
Dtx2	T	A	5: 136,058,057 (GRCm39)	M454K	possibly damaging	Het
Flg2	T	A	3: 93,127,513 (GRCm39)	S2142T	unknown	Het
Ganc	C	T	2: 120,276,996 (GRCm39)	T686M	possibly damaging	Het
Gria3	T	C	X: 40,677,369 (GRCm39)	V254A	possibly damaging	Het
H2-DMb2	G	T	17: 34,367,587 (GRCm39)	A3S	probably damaging	Het
H2-DMb2	A	G	17: 34,366,694 (GRCm39)	Y42C	probably damaging	Het
Mtrex	A	T	13: 113,051,023 (GRCm39)	I184K	probably damaging	Het
Myzap	T	C	9: 71,454,042 (GRCm39)	E343G	probably damaging	Het
Nap1l2	T	C	X: 102,228,922 (GRCm39)	D332G	probably benign	Het
Npr1	T	G	3: 90,365,669 (GRCm39)	D628A	probably damaging	Het
Raet1e	T	C	10: 22,057,219 (GRCm39)	L181S	probably damaging	Het
Rnf43	G	T	11: 87,622,718 (GRCm39)	M606I	probably benign	Het
Serpinb6b	G	A	13: 33,162,049 (GRCm39)	D283N	possibly damaging	Het
Slit2	A	G	5: 48,374,785 (GRCm39)		probably null	Het
Supt5	C	T	7: 28,023,213 (GRCm39)	W323*	probably null	Het
Svep1	T	A	4: 58,068,760 (GRCm39)	I3009F	possibly damaging	Het
Tedc1	C	T	12: 113,126,808 (GRCm39)	R357*	probably null	Het
Tll1	T	C	8: 64,523,266 (GRCm39)	Y482C	probably benign	Het
Trappc8	G	A	18: 20,970,035 (GRCm39)	T985I	probably benign	Het
Zfp945	T	C	17: 23,071,359 (GRCm39)	K180R	probably damaging	Het

Other mutations in Gm53

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL02197:Gm53	APN	11	96,142,549 (GRCm39)	exon	noncoding transcript
R3790:Gm53	UTSW	11	96,142,477 (GRCm39)	exon	noncoding transcript
R4857:Gm53	UTSW	11	96,142,562 (GRCm39)	exon	noncoding transcript

Posted On

2013-06-21