Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02275:Gm5828'

287301

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm5828

Ensembl Gene

Gene Name

predicted gene 5828

Synonyms

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.370) question?

Stock #

IGL02275

Quality Score

Status

Chromosome

Chromosomal Location

16838503-16840362 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

T to A at 16839342 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: ENSMUST00000071842

SMART Domains

Protein: ENSMUSP00000136559
Gene: ENSMUSG00000091020

Domain	Start	End	E-Value	Type
low complexity region	60	74	N/A	INTRINSIC
low complexity region	143	163	N/A	INTRINSIC
low complexity region	174	182	N/A	INTRINSIC
low complexity region	207	218	N/A	INTRINSIC
HMG	222	292	1.88e-17	SMART
low complexity region	307	339	N/A	INTRINSIC
low complexity region	435	481	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 24 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700037C18Rik	T	A	16: 3,724,146 (GRCm39)	D130V	probably damaging	Het
4930596D02Rik	T	C	14: 35,533,880 (GRCm39)	T9A	probably benign	Het
Anapc1	C	A	2: 128,501,772 (GRCm39)	A757S	probably benign	Het
Bpifa6	A	T	2: 153,834,192 (GRCm39)	D328V	probably benign	Het
Cdh19	T	A	1: 110,853,616 (GRCm39)	K275I	probably benign	Het
Col18a1	A	G	10: 76,895,217 (GRCm39)	I1148T	possibly damaging	Het
Commd1	A	T	11: 22,850,017 (GRCm39)	V222D	probably damaging	Het
Crim1	T	A	17: 78,677,427 (GRCm39)	M876K	possibly damaging	Het
Dennd1b	C	A	1: 139,008,992 (GRCm39)	H232N	probably damaging	Het
Dhx57	T	C	17: 80,582,268 (GRCm39)	T393A	probably benign	Het
Dnai7	T	C	6: 145,123,090 (GRCm39)	Y592C	probably damaging	Het
Gabrb2	G	T	11: 42,482,721 (GRCm39)	R193L	probably benign	Het
Gm6483	C	T	8: 19,741,629 (GRCm39)	P55S	probably damaging	Het
Hsp90ab1	T	C	17: 45,879,364 (GRCm39)	Y619C	possibly damaging	Het
Kctd19	A	G	8: 106,123,006 (GRCm39)	I136T	probably damaging	Het
Or2n1	G	T	17: 38,486,577 (GRCm39)	V201L	probably benign	Het
Or2w6	A	C	13: 21,843,170 (GRCm39)	F108V	probably benign	Het
Sel1l	T	C	12: 91,781,789 (GRCm39)	Y532C	probably damaging	Het
Sirpb1a	A	G	3: 15,475,469 (GRCm39)		probably null	Het
Ush2a	C	T	1: 187,995,466 (GRCm39)	T79M	possibly damaging	Het
Usp24	T	C	4: 106,244,690 (GRCm39)	V1215A	probably damaging	Het
Vdac3-ps1	T	C	13: 18,205,379 (GRCm39)		noncoding transcript	Het
Vmn2r75	T	C	7: 85,814,348 (GRCm39)	T382A	probably benign	Het
Vps53	T	C	11: 75,937,949 (GRCm39)	Y728C	probably benign	Het

Other mutations in Gm5828

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01143:Gm5828	APN	1	16,840,172 (GRCm39)	exon	noncoding transcript
IGL01751:Gm5828	APN	1	16,840,208 (GRCm39)	exon	noncoding transcript
IGL02400:Gm5828	APN	1	16,840,042 (GRCm39)	exon	noncoding transcript
IGL02480:Gm5828	APN	1	16,839,766 (GRCm39)	exon	noncoding transcript
R0143:Gm5828	UTSW	1	16,838,579 (GRCm39)	exon	noncoding transcript
R1245:Gm5828	UTSW	1	16,839,353 (GRCm39)	exon	noncoding transcript
R1405:Gm5828	UTSW	1	16,839,768 (GRCm39)	exon	noncoding transcript
R1514:Gm5828	UTSW	1	16,839,583 (GRCm39)	exon	noncoding transcript
R1644:Gm5828	UTSW	1	16,839,485 (GRCm39)	exon	noncoding transcript
R2118:Gm5828	UTSW	1	16,840,199 (GRCm39)	exon	noncoding transcript
R2290:Gm5828	UTSW	1	16,838,568 (GRCm39)	exon	noncoding transcript
R3428:Gm5828	UTSW	1	16,838,838 (GRCm39)	exon	noncoding transcript
R3962:Gm5828	UTSW	1	16,838,868 (GRCm39)	exon	noncoding transcript
R4657:Gm5828	UTSW	1	16,839,642 (GRCm39)	exon	noncoding transcript
R5067:Gm5828	UTSW	1	16,839,516 (GRCm39)	exon	noncoding transcript

Posted On

2015-04-16